CA2776954A1

CA2776954A1 - Combinatorial libraries based on c-type lectin domain

Info

Publication number: CA2776954A1
Application number: CA2776954A
Authority: CA
Inventors: Martha Wild; Anke Kretz-Rommel; Katherine Bowdish; Mark Renshaw
Original assignee: Anaphore Inc
Current assignee: Bird Rock Bio Inc
Priority date: 2009-10-09
Filing date: 2010-02-10
Publication date: 2011-04-14
Also published as: WO2011043834A1; EP2486132A1; JP2013507123A; CN102686727A

Abstract

This invention relates to polypeptide libraries comprising polypeptides having a C-type lectin domain (CTLD) with a randomized loop region, as well as nucleic acid libraries comprising nucleic acid molecules encoding such polypeptides. The invention also relates to methods for generating the randomized polypeptides and the polypeptide libraries. The invention further relates to methods of screening the polypeptide and nucleic acid libraries based on the specific binding of the modified CTLDs to a target molecule of interest. The invention also relates to polypeptides derived from such libraries that bind to target molecules of interest.

Description

Combinatorial Libraries Based on C-type Lectin Domain CROSS-REFERENCE TO RELATED APPLICATION

[001 ] This application is a continuation-in-part of U.S. Application Serial No. 12/577067, filed on October 9, 2009 and a continuation-in-part of International Application PCT
US09/60271, filed on October 9, 2009, all of which applications are incorporated by reference herein in their entireties.

SEQUENCE LISTING STATEMENT

[002] The sequence listing is filed in this application in electronic format only and is incorporated by reference herein. The sequence listing text file "09-493 Subst_SegList.txt" was created on March 21, 2010, and is 385 kilobytes in size.

FIELD OF THE INVENTION

[003] This invention relates to polypeptide libraries comprising polypeptides having a C-type lectin domain (CTLD) with a randomized loop region, as well as nucleic acid libraries comprising nucleic acid molecules encoding such polypeptides. The invention also relates to methods for generating the randomized polypeptides and the polypeptide libraries. The invention further relates to methods of screening the polypeptide and nucleic acid libraries based on the specific binding of the modified CTLDs to a target molecule of interest. The invention also relates to polypeptides derived from such libraries that bind to target molecules of interest.
BACKGROUND OF THE INVENTION

[004] The C-type lectin-like domain (CTLD) is a protein motif that has been identified in a number of proteins isolated from a variety of animal species (reviewed in Drickamer and Taylor (1993) and Drickamer (1999)). Initially, the CTLD domain was identified as a domain common to the so-called C-type lectins (calcium-dependent carbohydrate binding proteins) and named "Carbohydrate Recognition Domain" ("CRD"). More recently, it has become evident that this domain is shared among many eukaryotic proteins, of which several do not bind sugar moieties, and hence, the canonical domain has been named "CTLD."

RECTIFIED SHEET (RULE 91) ISA/EP

[005] CTLDs have been reported to bind a wide diversity of compounds, including carbohydrates, lipids, proteins, and even ice (Aspberg et al. (1997), Bettler et al. (1992), Ewart et al. (1998), Graversen et al. (1998), Mizumo et al. (1997), Sano et al. (1998), and Tormo et al.
(1999)). While some proteins contain a single copy of the CTLD, other proteins contain from two to multiple copies of the domain. In the physiologically functional unit, multiplicity in the number of CTLDs is often achieved by assembling single copy protein protomers into larger structures.

[006] The CTLD contains approximately 120 amino acid residues and, characteristically, contains two or three intra-chain disulfide bridges. Although the primary sequences of CTLDs from different proteins share relatively low amino acid sequence homology, the secondary and tertiary structures of a number of CTLDs are similar, resulting in a highly conserved three dimensional structure, in which the structural variability is essentially confined to the CTLD
loop-region. The CTLD loop region, which typically contains up to five loops, plays a role in ligand and calcium binding. Several CTLDs contain either one or two binding sites for calcium and most of the side chains which interact with calcium are located in the loop-region.

[007] Based on available three-dimensional structural information, the canonical CTLD is characterized by seven main secondary structure elements (five [3-strands and two a-helices) sequentially appearing in the following order: 01; al; a2; 02; 03; 04; and 05 (FIG. 1). In CTLDs for which the three dimensional structures have been determined, the (3-strands are arranged in two anti-parallel (3-sheets, one composed of (31 and 05, the other composed of (i2, (33 and (34. An additional (3-strand, [30, often precedes (31 in the sequence and, where present, forms an additional strand integrating with the 3l, (35 sheet. Further, two disulfide bridges, one connecting al and (35 (C,-Civ, FIG. 1) and one connecting (33 and the polypeptide segment connecting (34 and (35 (C11-C111, FIG. 1) are invariantly found in all CTLDs characterized so far.

[008] In the CTLD three-dimensional structure, the conserved secondary and tertiary structural elements form a compact scaffold for a number of loops, which in the present context collectively are referred to as the "loop-region," protruding out from the core. The primary structure of the loop. region of the CTLDs is organized into two segments, loop segment A (LSA) and loop segment B (LSB). LSA represents the long polypeptide segment connecting [32 and (33 RECTIFIED SHEET (RULE 91) ISA/EP

which often lacks regular secondary structure and contains up to four loops.
LSB represents the polypeptide segment connecting the (3-strands (i3 and (34. A schematic of a CTLD, including the loop region, is shown in FIGs 4-6. Residues in LSA, together with single residues in (34, have been shown to specify the Caz+- and ligand-binding sites of several CTLDs, including that of tetranectin. For example, mutagenesis studies, involving substitution of a single or a few residues, have shown that changes in binding specificity, Cat+-sensitivity and/or affinity can be accommodated by CTLD domains (Weis and Drickamer (1996), Chiba et al. (1999), Graversen et al. (2000)).

[009] Tetranectin is a trimeric glycoprotein (Holtet et a). (1997), Nielsen et al. (1997)) which has been isolated from human plasma and found to be present in the extracellular matrix in certain tissues. Tetranectin is known to bind calcium, complex polysaccharides, plasminogen, fibrinogen/fibrin, and apolipoprotein (a). The interaction with plasminogen and apolipoprotein (a) is mediated by the kringle 4-protein domain therein. This interaction is known to be sensitive to calcium and to derivatives of the amino acid lysine (Graversen et al.
(1998)).

[010] A human tetranectin gene has been characterized, and both human and murine tetranectin cDNA clones have been isolated. The mature protein of both the human and murine tetranectin comprises 181 amino acid residues. See US Patent Application Publication 2007/0154901, which is incorporated here in its entirety. The three dimensional structures of full length recombinant human tetranectin and of the isolated tetranectin CTLD have been determined independently in two separate studies (Nielsen et al. (1997) and Kastrup et at. (1998)).
Tetranectin is a two- or possibly three-domain protein, i.e. the main part of the polypeptide chain comprises the CTLD
(amino acid residues G1y53 to Val] 81), whereas the region Leu26 to Lys52 encodes an alpha-helix governing trimerization of the protein via the formation of a homotrimeric parallel coiled coil. The polypeptide segment Glul to G1u25 contains the binding site for complex polysaccharides (Lys6 to Lys 15) (Lorentsen et at. (2000)) and appears to contribute to stabilization of the trimeric structure (Holtet et al. (1997)). The two amino acid residues Lys148 and Glul50, localized in loop 4, and Asp165 (localised in [i4) have been shown to be of critical importance for plasminogen kringle 4 binding, with residues Ile140 (in loop 3) and Lys 166 and Arg167 (in (34) shown to be of importance as well (Graversen et at. (1998)).
Substitution of Thr149 (in loop 4) with an aromatic residue has been shown to significantly increase affinity of RECTIFIED SHEET (RULE 91) ISA/EP

tetranectin to kringle 4 and to increase affinity for plasminogen kringle 2 to a level comparable to the affinity of wild type tetranectin for kringle 4 (Graversen et al. (2000)).
Trimerizable truncations of tetranectin have been described. See US 2010/0028995, filed April 8, 2009, which is incorporated by reference herein in its entirety.

[011] A number of other proteins having CTLDs are known, including the following non-limiting examples: lithostatin, mouse macrophage galactose lectin, Kupffer cell receptor, chicken neurocan, perlucin, asialoglycoprotein receptor, cartilage proteoglycan core protein, IgE Fc receptor, pancreatitis-associated protein, mouse macrophage receptor, Natural Killer group, stem cell growth factor, factor IX/X binding protein, mannose binding protein, bovine conglutinin, bovine CL43, collectin liver 1, surfactant protein A, surfactant protein D, e-selectin, tunicate c-type lectin, CD94 NK receptor domain, LY49A NK receptor domain, chicken hepatic lectin, trout c-type lectin, HIV gp 120-binding c-type lectin, dendritic cell immunoreceptor, and many snake venom proteins.

[012] The variation of binding site configuration among naturally occurring CTLDs shows that their common core structure can accommodate many essentially different configurations of the ligand binding site (see, e.g., US 2007/0275393, which is incorporated by reference herein).
CTLDs are therefore particularly well suited to serve as a basis for constructing new and useful protein products with desired binding properties to target molecules of interest.

[013] For example, the CTLDs (or CTLD-based protein products) have advantages relative to antibody derivatives as each binding site in a CTLD-based protein product is harbored in a single structurally autonomous protein domain. Also, the CTLD domains are resistant to proteolysis, and neither stability nor access to the ligand-binding site is compromised by the attachment of other protein domains to the N- or C-terminus of the CTLD.

[014] With respect to therapeutic uses, the CTLD-based protein products are identical to the corresponding natural CTLD protein already present in the body, and are therefore expected to elicit minimal immunological response in the patient. Single CTLDs are about half the mass of an antibody and may in some applications be advantageous as it may provide better tissue penetration and distribution, as well as a shorter half-life in circulation.
Multivalent formats of CTLD proteins may provide increased binding capacity and avidity and longer circulation half-RECTIFIED SHEET (RULE 91) ISA/EP

life.

[015] The present invention provides combinatorial CTLD polypeptide libraries and methods for identifying and isolating CTLDs to serve as a basis for constructing new and useful protein products with desired binding properties to target molecules of interest.

SUMMARY OF THE INVENTION

[016] In one aspect, the invention provides a combinatorial polypeptide library comprising polypeptide members having a C-type lectin domain (CTLD) with a randomized loop region, in which the randomized loop region has been modified from the native sequence of the CTLD.
The invention provides a combinatorial polypeptide library, and a library of nucleic acids encoding the library of polypeptides, comprising polypeptide members having a C-type lectin domain (CTLD) with a randomized loop region, wherein the loop region of the CTLD is randomized according to one of the following Schemes:

[017] (a) amino acid modifications in at least one of the four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise an insertion of at least one amino acid in Loop I and random substitution of at least five amino acids within Loop 1;

[018] (b) amino acid modifications in at least one of the four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise random substitution of at least five amino acids within Loop I and random substitution of at least three amino acids within Loop 2;

[019] (c) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise random substitution of at least seven amino acids within Loop 1 and at least one amino acid insertion in Loop 4;

[020] (d) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise at least one amino acid insertion in Loop 3 and random substitution of at least three amino acids within Loop 3;

[021] (e) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise a modification that combines two loops into a single loop, wherein the two combined loops are Loop 3 and Loop 4;

RECTIFIED SHEET (RULE 91) ISA/EP

[022] (f) amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise at least one amino acid insertion in Loop 4 and random substitution of at least three amino acids within Loop 4;

[023] (g) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD and in loop segment B (LSB), wherein the amino acid modifications comprise random substitution of at least five amino acid residues in Loop 3 and random substitution of at least three amino acids within Loop 5;

[024] (h) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise random substitution of at least one amino acid and insertion of at least six amino acids in Loop 3;

[025] (i) amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise a mixture of (1) random substitution of at least six amino acids in Loop 3 and (2) random substitution of at least six amino acids and at least one amino acid insertion in Loop 3; and [026] (j) amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise at least four or more amino acid insertions in at least one of the four loops in the loop segment A (LSA) or loop 5 in loop segment B (LSB) of the CTLD.

[027] In one aspect, the CTLD of the polypeptides of the library have the following secondary structure:

a. five J3-strands and two a-helices sequentially appearing in the order 01, al, a2, 02, 03, (i4, and 05, the [3-strands being arranged in two anti-parallel (3-sheets, one composed of J31 and (35, the other composed of J32, 03 and 04, b. at least two disulfide bridges, one connecting al and (35 and one connecting (33 and the polypeptide segment connecting (34 and (35, and c. a loop region containing loop segment A (LSA) and loop segment B (LSB) in which LSA connects (32 and (33, and LSB connects (33 and (34.

RECTIFIED SHEET (RULE 91) ISA/EP

[028] In various further aspects, the polypeptides of the library have a random substitution of the amino acid located adjacent the C-terminal end of Loop 2 in the C-terminal direction. Also, when the CTLD is from human tetranectin, the CTLD can further comprise random substitution of Arginine-130. Also, when the CTLD is from mouse tetranectin, the CTLD can further comprise random substitution of Leucine-130. In certain of the modifications of (a) - (j), when the CTLD is from human or mouse tetranectin, the CTLD can further comprise a random substitution of proline 144.

[029) In various further embodiments, the polypeptides of the library can have random substitution of one or more amino acids involved in calcium coordination and/or plasminogen binding. For example, when the CTLD is from tetranectin, the CTLD can further comprise substitution of Lysine-148 to Alanine (in Loop 4).

[030] In certain embodiments, when the combinatorial library has the modified CTLD of Scheme (a), the amino acid modifications comprise two amino acid insertions in Loop I and random substitution of at least five amino acids within Loop 1. In other embodiments, when the combinatorial library has the modified CTLD of scheme (a) and the CTLD is from human tetranectin, the amino acid modifications comprise at least one amino acid insertion in Loop 1, random substitution of at least five amino acids within Loop 1, and include a random substitution of Arginine 130. In one specific embodiment, when the combinatorial library has the modified CTLD of scheme (a) and the CTLD is from human tetranectin, the amino acid modifications comprise two amino acid insertions in Loop 1, random substitution of five amino acids within Loop 1, and a random substitution of Arginine 130. In one specific embodiment, when the combinatorial library has the modified CTLD of scheme (a) and the CTLD is from mouse tetranectin, the amino acid modifications comprise two amino acid insertions in Loop 1, random substitution of five amino acids within Loop 1, and a random substitution of Leucine 130.1n. any of the embodiments for scheme (a), the amino acid modifications can further comprise a substitution of Lysine-148 to Alanine.

(031] In certain embodiments, when the combinatorial library has the modified CTLD of Scheme (b) and the CTLD is from human tetranectin, the amino acid modifications include random substitutions of at least five amino acids in Loop 1, random substitution of at least three RECTIFIED SHEET (RULE 91) ISA/EP

amino acids in Loop 2, and include a random substitution of Arginine 130. In one embodiment, when the combinatorial library has the modified CTLD of Scheme (b) and the CTLD is from human tetranectin, the amino acid modifications include random substitutions of five amino acids in Loop 1, random substitution of three amino acids in Loop 2, and a random substitution of Arginine 130. In certain other embodiments, when the combinatorial library has the modified CTLD of Scheme (b) and the CTLD is from mouse tetranectin, the amino acid modifications include random substitutions of at least five amino acids in Loop 1, random substitution of at least three amino acids in Loop 2, and include a random substitution of Leucine 130. In one embodiment, when the combinatorial library has the modified CTLD of Scheme (b) and the CTLD is from mouse tetranectin, the amino acid modifications include random substitutions of five amino acids in Loop 1, random substitution of three amino acids in Loop 2, and a random substitution of Leucine 130. In any of the embodiments for scheme (b), the amino acid modifications can further comprise a substitution of Lysine-1 48 to Alanine.
In other specific embodiments, individual members of the combinatorial library include loop regions including any or all of the polyeptpide sequences provided by Table 3 in the Examples below.

[032] In certain embodiments, when the combinatorial library has the modifications of Scheme (c), the amino acid modifications optionally further comprise random substitution of at least two amino acids. In certain other embodiments, when the combinatorial library has the modifications of Scheme (c), the amino acid modifications comprise three amino acid insertions within Loop 4 and optionally further comprise random substitution of at least two amino acids. In one embodiment, the amino acid modifications comprise random substitution of at least seven amino acids within Loop 1, at least three amino acid insertions in Loop 4, and random substitution of at least two amino acids within Loop 4. In one specific embodiment, the amino acid modifications comprise random substitution of seven amino acids within Loop 1, three amino acid insertions in Loop 4, and random substitution of two amino acids within Loop 4. In other specific embodiments, individual members of the combinatorial library include loop regions including any or all of the polyeptpide sequences provided by Table 3 in the Examples below.

[033] In other embodiments, when the combinatorial library has the modified CTLD of Scheme (d), the amino acid modifications can further comprise at least one amino acid insertion in Loop 4, and can further comprise random substitution of at least three amino acids within Loop 4. In RECTIFIED SHEET (RULE 91) ISA/EP

any of the described embodiments for scheme (d), the amino acid modifications can comprise three amino acid insertions in Loop 3. In any of the described embodiments for scheme (d), the amino acid modifications can comprise three amino acid insertions in Loop 4.
Thus, in certain embodiments, the amino acid modifications comprise random substitution of at least three amino acids within Loop 3, random substitution of at least three amino acids within Loop 4, at least one amino acid insertion in Loop 3 and at least one amino acid insertion in Loop 4. In certain .embodiments, the amino acid modifications comprise random substitution of at least three amino acids within Loop 3, random substitution of at least three amino acids within Loop 4, at least three amino acid insertions in Loop 3 and at least three amino acid insertions in Loop 4. In one specific embodiment, the amino acid modifications comprise random substitution of three amino acids within Loop 3, random substitution of three amino acids within Loop 4, three amino acid insertions in Loop 3, and three amino acid insertions in Loop 4. In other specific embodiments, individual members of the combinatorial library include loop regions including any or all of the polyeptpide sequences provided by Table 3 in the Examples below.

[034] In certain embodiments, when the members of the combinatorial library have the modified CTLD of Scheme (e), the amino acid modifications comprise random substitution of at least six amino acids within Loop 3 and random substitution of at least four amino acids within Loop 4. In one specific embodiment, the amino acid modifications comprise random substitution of six amino acids within Loop 3 and random substitution of four amino acids within Loop 4. In any of the embodiments for scheme (e), when the CTLD is from human tetranectin, the amino acid modifications can further comprise random substitution of Proline-144. In one specific embodiment, when the CTLD is from human tetranectin, the amino acid modifications comprise random substitution of six amino acids within Loop 3, random substitution of four amino acids within Loop 4, and a random substitution of proline 144, resulting in a combined Loop 3 and Loop 4 amino acid sequence, comprising, for example, NWEXXXXXXX XGGXXXN (SEQ
ID
NO: 578), wherein X is any amino acid and wherein the amino acid sequence of SEQ ID NO:
578 forms a single Loop region. In other specific embodiments, individual members of the combinatorial library include loop regions including any or all of the polyeptpide sequences provided by Table 3 in the Examples below.

[035] In other embodiments, when the combinatorial library has the modified CTLD of Scheme RECTIFIED SHEET (RULE 91) ISA/EP

(t), the amino acid modifications comprise four amino acid insertions in Loop 4. In one embodiment, when the combinatorial library has the modified CTLD of Scheme (f), the amino acid modifications comprise at least four amino acid insertions in Loop 4 and random substitution of at least three amino acids within Loop 4. In one specific embodiment, the amino acid substitutions comprise four amino acid insertions in Loop 4 and random substitution of three amino acids within Loop 4. In other specific embodiments, individual members of the combinatorial library include loop regions including any or all of the polyeptpide sequences provided by Table 3 in the Examples below.

[036] In other embodiments, when the combinatorial library has the modified CTLD of Scheme (g), and the CTLD is from tetranectin, the amino acid modifications can further comprise one or more amino acid modifications in Loop 4 that modulates plasminogen binding affinity of the CTLD, for example, the substitution of Lysine 148 to Alanine. Thus, in certain embodiments, when the CTLD is from human or mouse tetranectin, the amino acid modifications comprise random substitution of at least five amino acid residues in Loop 3, random substitution of at least three amino acid residues in Loop 5, and substitution of Lysine 148 to Alanine in Loop 4. In one specific embodiment, the amino acid modifications comprises random substitution of five amino acid residues in Loop 3 and random substitution of three amino acid residues in Loop 5, and, in another specific embodiment, when the CTLD is from human or mouse tetranectin, the amino acid modifications further comprise substitution of Lysine 148 to Alanine in Loop 4. In other specific embodiments, individual members of the combinatorial library include loop regions including any or all of the polyeptpide sequences provided by Table 3 in the Examples below.

[037) In certain embodiments, when the combinatorial library has the modified CTLD of Scheme (h) and the CTLD is from tetranectin, the amino acid modifications can further comprise one or more amino acid modifications in Loop 4 that modulates plasminogen binding affinity of the CTLD, for example, the substitution of lysine 148 to Alanine. In certain embodiments when the CTLD is from human or mouse tetranectin, the members of the combinatorial library have random substitution of at least one amino acid and insertion of at least six amino acids in Loop 3, and substitution of Lysine 148 to Alanine in Loop 4. In one specific embodiment, when the combinatorial library has the modified CTLD of Scheme (h), the amino acid modifications comprise random substitution of one amino acid and insertion of six amino acids in Loop 3. In RECTIFIED SHEET (RULE 91) ISA/EP

one specific embodiment, when the CTLD is from human or mouse tetranectin, the members of the combinatorial library have random substitution of one amino acid and insertion of six amino acids in Loop 3, and substitution of lysine 148 to alanine in Loop 4. In any of these embodiments when the CTLD is from human or mouse tetranectin, one of the substitutions is the substitution of Isoleucine 140. In other specific embodiments, individual members of the combinatorial library include loop regions including any or all of the polyeptpide sequences provided by Table 3 in the Examples below.

[038] In one embodiment, when the combinatorial library has the modified CTLD
of Scheme (i), the amino acid modifications comprise a mixture of random substitution of six amino acids in Loop 3, random substitution of six amino acids and one amino acid insertion in Loop 3, and random substitution of six amino acids and two amino acid insertions in Loop 3. In any of the embodiments of scheme (i), when the CTLD is from tetranectin, the amino acid modifications further comprise a substitution of Lysine 148 to Alanine in Loop 4.

[039] In further aspects of the invention, the polypeptide members of the combinatorial polypeptide library have one or more amino acid modifications in any combination of two, three, four, or five of the loops in loop segment A (LSA) and loop segment B (LSB).
The polypeptide members can also comprise a CTLD region having amino acid modifications in regions outside of the LSA and LSB. In other specific embodiments, individual members of the combinatorial library include loop regions including any or all of the polyeptpide sequences provided by Table 17 in the Examples below.

[040] In certain embodiments of the invention, the combinatorial library is composed of polypeptide members having modified loop regions in the CTLD from human or murine tetranectin. In certain embodiments, the polypeptide members can also have an N-terminal extension and/or a C-terminal extension of the CTLD. The N-terminal extension and/or C- -terminal extension can provide effector function, enzyme function, further binding function, or multimerizing function. In one embodiment, at least one of the N-terminal extension and the C-terminal extension includes the non-CTLD-portions of a native C-type lectin-like protein or C-type lectin or a C-type lectin lacking a functional transmembrane domain. In one embodiment, the proteins are multimers of a moiety comprising the CTLD.

RECTIFIED SHEET (RULE 91) ISA/EP

[041) In other embodiments of the invention, the polypeptide members can have additional alterations in the loop regions, introduced by peptide grafting or identified by panning, that can provide effector function, enzyme function, further binding function, or multimerising function.

[042] In other embodiments, the combinatorial library is composed of polypeptide members having modified loop regions in the CTLD region of a full-length human or murine tetranectin.
In certain embodiments, the polypeptide members can have an N-terminal extension of the trimerization domain of tetranectin. The N-terminal extension can provide effector function, enzyme function, further binding function, or multimerizing function. In one embodiment, the N-terminal extension is a peptide or a polypeptide with known function or a peptide identified by panning.

[043] In another aspect, the invention is directed to a library of nucleic acid molecules that encode any of the polypeptides described herein. In one embodiment, the invention provides a library of nucleic acid molecules encoding polypeptides having a CTLD with a randomized loop region, wherein the loop region of the CTLD is randomized according to any of the Schemes (a) - (i) described herein. In other embodiments, the invention provides a library of nucleic acid molecules encoding polypeptides having a CTLD randomized according to any of the Schemes (a) - (i) and having any of the further modifications or sequences described herein.

-[044] The library of nucleic acid molecules can be expressed in a display system having an observable phenotype that represents at least one property of the displayed expression products and the corresponding genotypes. Examples of suitable display systems include a phage display system; a yeast display system; a viral display system; a cell-based display system; a ribosome-linked display system; or a plasmid-linked display system.

[045] In another aspect, the invention is directed to a method for generating a combinatorial library of any of the polypeptides described herein. Thus, the invention provides a method for generating a combinatorial library of polypeptides having a CTLD with a randomized loop region, wherein the loop region of the CTLD is randomized according to any of the Schemes (a) - (i) described herein. In one embodiment, the method comprises generating at least one random mutation in at least one of the four loops in the LSA region of the CTLD. In another embodiment, the method comprises generating at least one random mutation in at least one of the RECTIFIED SHEET (RULE 91) ISA/EP

four loops in the LSA region and generating at least one random mutation in the loop in the LBA
region of the CTLD. The random mutation can be created by oligonucleotide-directed randomization, DNA shuffling by random fragmentation, loop shuffling, loop walking, or error-prone PCR mutagenesis and other methods known in the art. In other embodiments, the invention provides a method for generating a combinatorial library of polypeptides having a CTLD randomized according to any of the Schemes (a) - (j) and having any of the further modifications or sequences described herein.

[046] In another aspect, the invention is directed to a method for identifying and isolating a polypeptide having specific binding activity to a target molecule. In one embodiment, the method comprises providing a combinatorial library of polypeptides having a CTLD wherein the loop region of the CTLD is randomized according to any of the Schemes (a) -(j), contacting the combinatorial polypeptide library with the target molecule under conditions that allow for binding between a polypeptide and the target molecule; and isolating a polypeptide that binds to the target molecule. In another embodiment, the method comprises providing a combinatorial library of polypeptides having a CTLD randomized according to any of the Schemes (a) - (j) and any of the further modification or sequences described herein, contacting the combinatorial polypeptide library with the target molecule under conditions that allow for binding between a polypeptide and the target molecule; and isolating a polypeptide that binds to the target molecule. The method can further include a library of nucleic acid molecules encoding polypeptides of the combinatorial polypeptide library described herein, wherein the library of nucleic acids is expressed in a display system, wherein the display system comprises an observable phenotype that represents at least one property of the displayed expression products and the corresponding genotypes.

[047] The invention is also directed to a method for the identification and isolation of a polypeptide that specifically binds to a target using a library of nucleic acid molecules. In one embodiment, the invention provides a method for the identification and isolation of a polypeptide capable of specifically binding to a target comprising the steps of providing a library of nucleic acids encoding polypeptides having a CTLD with a randomized loop region, wherein the loop region of the CTLD is randomized according to any of Schemes (a) - (j), expressing the nucleic acid library in a display system to obtain an ensemble of polypeptides, in which the amino acid RECTIFIED SHEET (RULE 91) ISA/EP

residues at one or more sequence positions differ between different members of said ensemble of polypeptides, contacting the ensemble of polypeptides with said target, and isolating a polypeptide that is capable of specifically binding to said target. In other embodiments, the method comprises providing a library of nucleic acid molecules encoding polypeptides having a CTLD randomized according to any of the Schemes (a) - (j) and having any of the further modifications or sequences described herein.

[048] In another aspect, the invention provides a polypeptide having the scaffold structure of a C-type Lectin Like Domain (CTLD), wherein the polypeptide binds to a target other than a natural target for that CTLD and wherein the CTLD scaffold structure of the CTLD is modified according to any of the schemes (a) - (j). In one embodiment, the CTLD
scaffold structure is modified according to any of the schemes (a) - (j) and further comprises any of the further modifications described herein, for example, modifications outside the CTLD
loop region. In one embodiment, the polypeptide has the scaffold structure of the CTLD from human or mouse tetranectin and binds to a target other than plasminogen.

[049] The polypeptide can be produced using a combinatorial library of polypeptides having a CTLD, wherein the loop region of the CTLD is randomized according to any of the Schemes (a) - (j), contacting the combinatorial polypeptide library with the target molecule under conditions that allow for binding between a polypeptide and the target molecule; and isolating a polypeptide that binds to the target molecule, wherein the the target molecule is not the natural target for that CTLD. In one embodiment of this method, the CTLD is human or mouse tetranectin. In another embodiment of this method, the CTLD is randomized according to any of the Schemes (a) - (j) and comprises any of the further modifications described herein, for example, modifications outside the CTLD loop region.

BRIEF DESCRIPTION OF THE FIGURES

[050] Figure 1 depicts an alignment of the amino acid sequences of ten CTLDs of known three-dimensional structure. The sequence locations of main secondary structural elements are indicated above each sequence and labeled in sequential numerical order wherein "aX" denotes an a-helix number X, and (3Y denotes a (3-strand number Y. The four cysteine residues involved in the formation of the two conserved disulfide bridges of the CTLDs are indicated and RECTIFIED SHEET (RULE 91) ISA/EP

numbered as C1, Cn, Cm, and Civ, where the disulfide bridges are formed by C[-Crv and Cn-Ctn. The various loop regions in the human tetranectin sequence are indicated by underlining.
[051] The various CTLDs include: "hTN" (human tetranectin, Nielsen et al., (1997)); "MBP"
(mannose binding protein, Weis et al., (1991); Sheriff et al., (1994)); "SP-D"
(surfactant protein D, Hakansson et al., (1999)); "LY49A" (NK receptor LY49A, Tormo et al., (1999)); "Hl-ASR"
(H1 subunit of the asialoglycoprotein receptor, Meier et al., (2000)); "MMR-4"
(macrophage mannose receptor domain 4, Feinberg et al., (2000)); "IX-A" and "IX-B"
(coagulation factors IX/X-binding protein domain A and B, respectively, Mizuno et al., (1997);
"Lit" (lithostatine, Bertrand et al., (1996)); and "TU14" (tunicate C-type lectin, Poget et al., (1999)).

[052] Figure 2 depicts an alignment of the nucleotide and amino acid sequences of the coding regions of the mature forms of human and murine tetranectin with an indication of known secondary structural elements.

[053] Figure 3 depicts an alignment of several C-type lectin domains from tetranectins isolated from human (Swissprot P05452), mouse (Swissprot P43025), chicken (Swissprot Q9DDD4), bovine (Swissprot Q2KIS7), Atlantic salmon (Swissprot B5XCV4), frog (Swissprot Q5I0R9), zebrafish (GenBank XP_701303), and related CTLD homologues isolated from cartilage of cattle (Swissprot u22298) and reef shark (Swissprot p26258).

[054] Figure 4 depicts the three dimensional structure (ribbon format) for human tetranectin, depicting the secondary structural features of the protein. The structure was solved in the Cat+-bound form.

[055] Figure 5A depicts the three dimensional overlay structures of the CTLDs for human tetranectin (HTN) and several tetranectin homologues, including human mannose binding protein (MBP), rat mannose binding protein-C (MBP-C), human surfactant protein D, rat mannose binding protein-A (MBP-A), and rat surfactant protein A. The CTLD
overlay structures were generated using Swiss PDB Viewer DeepView v. 4Ø1 for MacIntosh using the three-dimensional structure of human tetranectin as a.template. Figure 5B
shows the corresponding amino acid sequences of the CTLDS for human tetranectin and the tetranectin homologues depicted in Figure 5A. In Figure B, 1 HUP = human mannose binding protein, RECTIFIED SHEET (RULE 91) ISA/EP

1 BV4A = rat mannose binding protein, 2GGUA = human surfactant protein D, I
KXOA= rat mannose binding protein A, IR13 = rat surfactant protein A.

[056] Figure 6A depicts the three dimensional overlay structures of the CTLDs for human tetranectin (HTN) and several tetranectin homologues, including human pancreatitis-associated protein, human dendritic cell-specific ICAM-3-grabbing non-integrin 2 (DC-SIGNR), rat aggrecan, mouse scavenger receptor, and human scavenger receptor. The CTLD
overlay structures were generated using Swiss PDB Viewer DeepView v. 4Ø1 for MacIntosh using the three-dimensional structure of human tetranectin as a template. Figure 6B
shows the corresponding amino acid sequences of the CTLDS for human tetranectin and the tetranectin homologues depicted in Figure 6A. In Figure 6B, 1 TDQB = rat aggrecan, 1 UVOA
= human pancreatitis-associated protein, 20X8A = human scavenger receptor, 20X9A =
mouse scavenger receptor, and I SL6A = human DC-SIGNR) [057] Figure 7 shows the PCR strategy for creating randomized loops in a CTLD.

[058] Figure 8 shows the DNA and amino acid sequence of the human tetranectin CTLD*
modified to contain restriction sites for cloning, indicating the Ca2+ binding sites. Restriction sites are underscored with solid lines. Loops are underlined with dashed lines. Calcium coordinating residues are in bold italics and include Site 1: D 116, El 20, GI
47, El 50, N151;
Site 2: Q143, D145, E150, D165. The CTLD domain starts at amino acid A45 in bold (i.e.
ALQTVCL...). Changes to the native tetranectin (TNCTLD) base sequence are shown in lower case. The restriction sites were created using silent mutations that did not alter the native amino acid sequence.

[059] Figure 9 depicts a non-limiting strategy for lengthening and introducing randomization in a CTLD loop region.

[060] Figure 10 shows the results of experiments measuring cell death in the presence of five DR5 ATRIMERsTM: 4a8c, 2ala, 1a7b, 9b3d and 8b6b. H2122 lung adenocamoma cells and A2780 ovarian carcinoma cells were incubated at 1 x 104 cells/well with DR5 ATRIMERsTM (20 g/ml,) or TRAIL (0.2 g/mL). Data are expressed as percent cell death relative to the respective buffer control.

RECTIFIED SHEET (RULE 91) ISA/EP

[0611 Figure 11 shows the results of an experiment comparing binding of the polypeptides of the invention and native human IL-23 to human IL-23R.

[062] Figure 12 shows the results of an experiment comparing IL-23-induced IL-17 production in the presence of ATRIMERTM complex 4G8 of the invention, native human IL-23, and Ustekinumab.

[063] Figure 13 shows the results of an experiment comparing IL-23 induced IL-17 production in the presence of ATRIMERTM complex 1 A4 of the invention and Ustekinumab.

[064] Figure 14 shows the results of an experiment comparing IL-12-induced IFNy production in the presence of ATRIMERTM complex 4G8 of the invention, native human IL-23, and Ustekinumab.

[065] Figure 15 shows the results of an experiment comparing Stat-3 phosphorylation in NKL
cell in in response to IL-23 and the the polypeptides of the invention.

[066] Figures 16A and 16B are tables showing experimental results associated with several ATRIMERTM polypeptide complexes of the invention.

DETAILED DESCRIPTION OF THE INVENTION
[067] Definitions [068] All scientific and technical terms used throughout the application should be understood to have their common scientific/technical meaning, unless specifically indicated otherwise.
Similarly when the singular form of a term or article is used, it should be understood to also encompass the plural form of that term or article.

[069] The terms "C-type lectin-like protein" and "C-type lectin" are used to refer to any protein or polypeptide present in or encoded in the genomes of any eukaryotic species, wherein the protein or polypeptide contains one or more C-type lectin domains (CTLDs) or one or more domains belonging to any subgroup of CTLD, (e.g., the CRDs, which can bind carbohydrate ligands). The definition includes membrane attached C-type lectin-like proteins and C-type lectins, "soluble" C-type lectin-like proteins and C-type lectins lacking a functional RECTIFIED SHEET (RULE 91) ISA/EP

transmembrane domain and variant C-type lectin-like proteins and C-type lectins in which one or more amino acid residues have been altered in vivo by glycosylation or any other post-synthetic modification, as well as any product that is obtained by chemical and enzymatic modification of C-type lectin-like proteins and C-type lectins. In the claims and throughout the specification certain alterations can be defined with reference to particular amino acid residue numbers of a CTLD or a CTLD-containing protein. See, Essentials of Glycobiology, second edition. Edited by A. Varki, R.D. Cummings, J.D. Esko, HH. Freeze, P. Stanley, C.R. Bertozzi, G.W. Hart, M.E.
Etzler. CHS Press.

[070] The CTLD consists of roughly 120 amino acid residues and, characteristically, contains two or three intra-chain disulfide bridges. Although the similarity at the amino acid sequence level between CTLDs from different proteins is relatively low, the three dimensional structures of a number of CTLDs have been found to be highly conserved, with the structural variability essentially confined to the loop-region, often defined by up to five loops.
Several CTLDs contain either one or two binding sites for calcium and most of the side chains which interact with calcium are located in the loop-region.

[071] On the basis of CTLDs for which three dimensional structural information is available, it has been inferred that the canonical CTLD is structurally characterized by seven main secondary-structure elements (i.e. five [3-strands and two a-helices) sequentially appearing in the order J31, al, a2, (i2, (33, (34, and 05. Figure 1 illustrates an alignment of the CTLDs of known three dimensional structures of ten C-type lectins. In all CTLDs for which three dimensional structures have been determined, the 0-strands are arranged in two anti-parallel (3-sheets, one composed of [31 and (35, the other composed of (32, (33 and 04. An additional J3-strand, (i0, often precedes (31 in the sequence and, where present, forms an additional strand integrating with the (31, [35-sheet. Further, two disulfide bridges, one connecting al and (35 (Ci-CN) and one connecting 03 and the polypeptide segment connecting 04 and 05 (C11-C111) are invariantly found in all CTLDs characterized to date.

[072] The conserved secondary structure elements (alpha helix and beta sheet) form a compact scaffold for a number of loops, which in the present context collectively are referred to as the "loop-region", protruding out from the core. In the primary structure of the CTLDs, these loops RECTIFIED SHEET (RULE 91) ISA/EP

are organized in two segments, loop segment A, LSA, and loop segment B, LSB.
LSA represents the long polypeptide segment connecting 02 and 03 that often lacks regular secondary structure and contains up to four loops. LSB represents the polypeptide segment connecting the (3-strands [33 and 04. Residues in LSA, together with single residues in 04, have been shown to specify the Cat+- and ligand-binding sites of several CTLDs, including that of tetranectin. For example, mutagenesis studies, involving substitution of one or a few residues, have shown that changes in binding specificity, Cat+-sensitivity and/or affinity can be accommodated by CTLD domains [073] As discussed herein, a number of proteins having CTLDs are known, including the following non-limiting examples: tetranectin, lithostatin, mouse macrophage galactose lectin, Kupffer cell receptor, chicken neurocan, perlucin, asialoglycoprotein receptor, cartilage proteoglycan core protein, IgE Fc receptor, pancreatitis-associated protein, mouse macrophage receptor, Natural Killer group, stem cell growth factor, factor IX/X binding protein, mannose binding protein, bovine conglutinin, bovine CL43, collectin liver 1, surfactant protein A, surfactant protein D, e-selectin, tunicate c-type lectin, CD94 NK receptor domain, LY49A NK
receptor domain, chicken hepatic lectin, trout c-type lectin, HIV gp 120-binding c-type lectin, and dendritic cell immunoreceptor. See U.S. 2007/0275393, which is incorporated by reference herein in its entirety.

[074] The terms "amino acid," "amino acids," and "amino acid residues" refer to all naturally occurring L-amino acids, as well as non-naturally occurring amino acids. This definition is meant to include norleucine, ornithine, and homocysteine. The naturally occurring L-amino acids can be classified according to the chemical composition and properties of their side chains.
They are broadly classified into two groups, charged and uncharged. Each of these groups is divided into subgroups to classify the amino acids more accurately: A. Charged Amino Acids -(A. 1. Acidic Residues): Asp, Glu; (A.2. Basic Residues): Lys, Arg, His, Orn;
B. Uncharged Amino Acids - (B. 1. Hydrophilic Residues): Ser, Thr, Asn, Gln; (B.2.
Aliphatic Residues): Gly, Ala, Val, Leu, Ile, Nle; (B.3. Non-polar Residues): Cys, Met, Pro, Hcy; (B.4.
Aromatic Residues): Phe, Tyr, Trp.

[075] A "non-natural amino acid " or "non-naturally occuring amino acid"
refers to an amino acid that is not one of the 20 common amino acids including, for example, amino acids that RECTIFIED SHEET (RULE 91) ISA/EP

occur by modification (e.g. post-translational modifications) of a naturally encoded amino acid (including but not limited to, the 20 common amino acids or pyrolysine and selenocysteine) but are not themselves naturally incorporated into a growing polypeptide chain by the translation complex. Examples of such non-naturally-occurring amino acids include, but are not limited to, N-acetylglucosaminyl-L-serine, N-acetylglucosaminyl-L-threonine, and O-phosphotyrosine.
[076] Many of the unnatural amino acids suitable for use in the present invention are commercially available, e.g., from Sigma (USA) or Aldrich (Milwaukee, Wis., USA). Those that are not commercially available are optionally synthesized as provided herein or as provided in various publications or using standard methods known to those of skill in the art. For organic synthesis techniques, see, e.g., Organic Chemistry by Fessendon and Fessendon, (1982, Second Edition, Willard Grant Press, Boston Mass.); Advanced Organic Chemistry by March (Third Edition, 1985, Wiley and Sons, New York); and Advanced Organic Chemistry by Carey and Sundberg (Third Edition, Parts A and B, 1990, Plenum Press, New York).
Additional publications describing the synthesis of unnatural amino acids include, e.g., entitled "In vivo incorporation of Unnatural Amino Acids;" Matsoukas et al., (1995) J. Med.
Chem., 38, 4660-4669; King, F. E. & Kidd, D. A. A. (1949) A New Synthesis of Glutamine and of. gamma. -Dipeptides of Glutamic Acid from Phthylated Intermediates. J.
Chem. Soc., 3315-3319; Friedman, O. M. & Chatterrji, R. (1959) Synthesis of Derivatives of Glutamine as Model Substrates for Anti-Tumor Agents. J. Am. Chem. Soc. 81, 3750-3752; Craig, J.
C. et al. (1988) Absolute Configuration of the Enantiomers of 7-Chloro-4[[4-(diethylamino)-1-methylbutyl]amino]quinoline (Chloroquine). J. Org. Chem. 53, 1167-1170;
Azoulay, M., Vilmont, M. & Frappier, F. (1991) Glutamine analogues as Potential Antimalarials, Eur. J. Med.
Chem. 26, 201-5; Koskinen, A. M. P. & Rapoport, H. (1989) Synthesis of 4-Substituted Prolines as Conformationally Constrained Amino Acid Analogues. J. Org. Chem. 54, 1859-1866;
Christie, B. D. & Rapoport, H. (1985) Synthesis of Optically Pure Pipecolates from L-Asparagine. Application to the Total Synthesis of (+)-Apovincamine through Amino Acid Decarbonylation and Iminium Ion Cyclization. J. Org. Chem. 1989: 1859-1866;
Barton et al., (1987) Synthesis of Novel a-Amino-Acids and Derivatives Using Radical Chemistry: Synthesis of L-and D-a-Amino-Adipic Acids, L-a-aminopimelic Acid and Appropriate Unsaturated Derivatives. Tetrahedron Lett. 43: 4297-4308; and, Subasinghe et al., (1992) Quisqualic acid RECTIFIED SHEET (RULE 91) ISA/EP

analogues: synthesis of beta-heterocyclic 2-aminopropanoic acid derivatives and their activity at a novel quisqualate-sensitized site. J. Med. Chem. 35: 4602-7. See also, US
2004/0198637 and US 2005/0170404, each of which is incorporated by reference herein in their entirety.

[077) The terms "amino acid modification(s)" and "modification(s)" refer to amino acid substitutions, deletions or insertions or any combinations thereof in an amino acid sequence relative to the native sequence. Substitutional variants herein are those that have at least one amino acid residue in a native CTLD sequence removed and a different amino acid inserted in its place at the same position. The substitutions may be single, where only one amino acid in the molecule has been substituted, or they may be multiple, where two or more amino acids have been substituted in the same molecule. Specific reference to more than one amino acid substitution in a CTLD refers to multiple substitutions in which each individual amino acid substitution can occur at any amino acid position within the CTLD, including consecutive and non-consecutive amino acid positions. Likewise, specific reference to more than one amino acid insertion or deletion in a CTLD refers to multiple insertions or deletions in which each individual amino acid insertion or deletion can occur at any amino acid position within the CTLD, including consecutive and non-consecutive amino acid positions.

[078] The terms "nucleic acid molecule encoding", "DNA sequence encoding", and "DNA
encoding" refer to the order or sequence of deoxyribonucleotides along a strand of deoxyribonucleic acid. The order of these deoxyribonucleotides determines the order of amino acids along the polypeptide chain. The DNA sequence thus encodes the amino acid sequence.
[079] The terms "randomize," "randomizing" and "randomized" as well as any similar terms used in any context to identify randomized polypeptide or nucleic acid sequences, refer to ensembles of polypeptide or nucleic acid sequences or segments, in which the amino acid residue or nucleotide at one or more sequence positions may differ between different members of the ensemble of polypeptides or nucleic acids, such that the amino acid residue or nucleotide occurring at each such sequence position may belong to a set of amino acid residues or nucleotides that may include all possible amino acid residues or nucleotides or any restricted subset thereof. The terms are often used to refer to ensembles in which the number of possible amino acid residues or nucleotides is the same for each member of the ensemble, but may also be RECTIFIED SHEET (RULE 91) ISA/EP

used to refer to such ensembles in which the number of possible amino acid residues or nucleotides in each member of the ensemble may be any integer number within an appropriate range of integer numbers.

[080] The terms "modulate" or "modulating" when used with reference to either the binding affinity of a CTLD to plasminogen, metal (e.g., Mgt+, Cat+, Zn2+, Mn2+, etc.) or any other target molecule refer to a change in the binding affinity of a modified CTLD
polypeptide to either plasminogen or metal ion or target molecule relative to the binding affinity of the native (unmodified) CTLD polypeptide. Thus, "modulating" includes increasing binding affinity, decreasing binding affinity, and/or abolishing or abrogating binding affinity (although not to the exclusion of the specific recitation of the terms "abolishing" or" abrogating"
plasminogen, metal ion, or target molecule binding activity).

[081] When referring to a binding pair, such as ligand/receptor, antibody/antigen, or other binding pair, binding is measured in a binding reaction which is determinative of the presence of a member of a binding pair in a heterogeneous population of another member of the binding pair. Under designated conditions, "specific binding" occurs when one member of the binding pair binds to another member of the binding pair in a heterologous population and does not bind in a significant amount to other proteins or polypeptides present in the sample. Specific binding can be measured using the methods described herein, including Biacore and ELISA.

[082] The term "IX-2 Library" refers to a combinatorial polypeptide library comprising polypeptide members that have a C-type lectin domain (CTLD) comprising amino acid modifications in at least one of the four loops in the LSA of the CTLD, wherein the amino acid modifications comprise at least two amino acid insertions in Loop 1 and random substitution of at least five amino acids within Loop 1 of the CTLD.

[083] The term "1-2 library" refers to a combinatorial polypeptide library comprising polypeptide members that have a C-type lectin domain (CTLD) comprising amino acid modifications in at least one of the four loops in the LSA of the CTLD, wherein the amino acid modifications comprise random substitution of at least five amino acids within Loop 1 and random substitution of at least three amino acids within Loop 2.

RECTIFIED SHEET (RULE 91) ISA/EP

[084] The term "1-4 library" refers to a combinatorial polypeptide library comprising polypeptide members that have a C-type lectin domain (CTLD) comprising amino acid modifications in at least one of the four loops in the LSA of the CTLD, wherein the amino acid modifications comprise random substitution of at least seven amino acids within Loop 1, at least three amino acid insertions in Loop 4, and random substitution of at least two amino acids.

[085] The term "3X library" refers to a combinatorial polypeptide library comprising polypeptide members that have a C-type lectin domain (CTLD) comprising amino acid modifications in at least one of the four loops in the LSA of the CTLD, wherein the amino acid modifications comprise a mixture of random substitution of at least six amino acids, random substitution of at least six amino acids and at least one amino acid substitution, and random substitution of at least six amino acids and at least two amino acid substitutions in Loop 3.
[086] The term "3-4X library" refers to a combinatorial polypeptide library comprising polypeptide members that have a C-type lectin domain (CTLD) comprising amino acid modifications in at least one of the four loops in the LSA of the CTLD, wherein the amino acid modifications comprise at least three amino acid insertions in Loop 3 and random substitution of at least three amino acids within Loop 3 and comprise at least three amino acid insertions in Loop 4 and random substitution of at least three amino acids within Loop 4.

[087] The term "3-4 combo library" refers to a combinatorial polypeptide library comprising polypeptide members that have a C-type lectin domain (CTLD) comprising amino acid modifications in at least one of the four loops in the LSA of the CTLD, wherein the amino acid modifications comprise a modification that combines two loops into a single loop, wherein the two combined loops are Loop 3 and Loop 4.

[088] The term "4 library" refers to a combinatorial polypeptide library comprising polypeptide members that have a C-type lectin domain (CTLD) comprising amino acid modifications in at least one of the four loops in the LSA of the CTLD, wherein the amino acid modifications comprise at least four amino acid insertions in Loop 4 and random substitution of at least three amino acids within Loop 4.

[089] The term "3-5 library" refers to a combinatorial polypeptide library comprising RECTIFIED SHEET (RULE 91) ISA/EP

polypeptide members that have a C-type lectin domain (CTLD) comprising amino acid modifications in at least one of the four loops in the LSA of the CTLD, wherein the amino acid modifications comprise random substitution of at least five amino acids within Loop 3 and random substitution of at least three amino acids within Loop 5.

[090] The term "Loop 3X loop library" refers to a combinatorial polypeptide library comprising polypeptide members that have a C-type lectin domain (CTLD) comprising amino acid modifications in at least one of the four loops in the LSA of the CTLD, wherein the amino acid modifications comprise random substitution of at least one amino acid and at least six amino acid insertions.

[091] Combinatorial Polypeptide Libraries with modified CTLD

[092] The invention relates generally to a combinatorial polypeptide library comprising polypeptide members having a C-type lectin domain (CTLD) with a randomized loop region, in which the randomized loop region has been modified from the native sequence of the CTLD.
The randomized loop region of the CTLD can comprise one or more amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD and can further comprise one or more amino acid modifications in the loop in Loop Segment B (LSB) (also known as loop 5). The invention also relates to methods for generating and using the randomized combinatorial polypeptide libraries. By applying standard combinatorial methods known in the chemical, recombinant protein and antibody arts, the libraries and methods of the invention allow for the generation, screening, and identification of protein products that exhibit binding specificity to target molecules of interest.

[093] The variation of binding site configuration among naturally occurring CTLDs shows that their common core structure can accommodate many essentially different configurations of the ligand binding site (see, e.g., US 2007/0275393). CTLDs are therefore particularly well suited to serve as a basis for constructing such new and useful protein products with desired binding properties. Accordingly, while in one aspect the invention relates to combinatorial polypeptide libraries comprising modifications to the loop region of the CTLD (LSA and LSB), other modifications to the general CTLD core structure (i.e., the R-strands and a-helices) can be made without affecting the utility of the libraries described herein. One of skill in the art can target RECTIFIED SHEET (RULE 91) ISA/EP

particular modifications in the CTLD core structure that will retain CTLD
functionality. For example, based on secondary and tertiary structures of various polypeptides comprising CTLDs, hydropathy, charge (ionic), and hydrogen bonding interactions can all be taken into consideration, and appropriate substitutions made which retain CTLD function.
Such modifications include conservative amino acid substitutions. In embodiments that comprise variants, such as deletion, insertion, or substitution variants in the region outside of the loop region of the CTLD, the percent identity can be as low as 50%. In other embodiments comprising such variation within the CTLD region, variants are at least 80%
identical to any given CTLD sequence, or CTLD consensus sequence. In certain embodiments such variants are at least 85%, 86%, 87%, 88%, 89%,90%,9l%,92%,93%2 94%,95%,,96%,97%,98%, or 99%, identical to any CTLD sequence, or CTLD consensus sequence.

[094] The CTLD used in the combinatorial libraries can be derived from any CTLD. Examples of suitable CTLDs are CTLDs described herein (i.e., Figures 1-3) and in US
2007/0275393, which is incorporated by reference herein in its entirety (i.e., Figure 1 and Table 1) and CTLDs otherwise known in the art. In certain embodiments, the CTLD has the following secondary structure: five (3-strands and two a-helices sequentially appearing in the order (31, al, a2, (32, [33, (34, and (35, the 3-strands being arranged in two anti-parallel (3-sheets, one composed of (31 and (35, the other composed of (i2, (33 and (34, at least two disulfide bridges, one connecting al and (35 and one connecting (33 and the polypeptide segment connecting (34 and (35, and a loop region containing loop segment A (LSA) and loop segment B (LSB) in which LSA connects (32 and (33, and LSB connects (33 and (34.

[095] In particular embodiments, the CTLD sequence is a human or murine tetranectin CTLD
sequence that is modified according to the invention. FIG. 2 shows the alignment of the nucleic acid and polypeptide sequences of human and mouse tetranectin CTLDs. In other embodiments, the CTLD is from a variety of peptides, for example, those shown in FIG. 3, which shows an alignment of several CTLDs from tetranectins isolated from human (Swissprot P05452), mouse (Swissprot P43025), chicken (Swissprot Q9DDD4), bovine (Swissprot Q2KIS7), Atlantic salmon (Swissprot B5XCV4), frog (Swissprot Q5IOR9), zebrafish (GenBank XP -701303), and related CTLD homologues isolated from cartilage of cattle (Swissprot u22298) and reef shark (Swissprot p26258).

RECTIFIED SHEET (RULE 91) ISA/EP

[096] Thus, in a broad aspect, the invention provides a polypeptide library comprising polypeptide members that comprise a C-type lectin domain (CTLD), wherein the CTLD
comprises one or more amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, and/or in the loop in loop segment B (LSB) (Loop 5). Examples of polypeptide libraries comprising polypeptides having a C-type lectin domain comprising one or more amino acid modifications in at least one of.the five loops in the loop region (LSA and LSB) of the CTLD are described herein.

[097] In certain embodiments of the polypeptide libraries, the polypeptide members have CTLDs in which one, two, three, four, or five of the CTLD loops have one or more amino acid modifications, wherein the one or more modifications include at least one amino acid insertion that extends the loop region beyond its original length. In certain of these embodiments, the one or more modifications include from 1 to about 30 amino acid insertions (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 amino acid insertions) in any single loop in the loop region (LSA and LSB). In certain of these embodiments, the one or more modifications include at least one amino acid insertion in at least two of the five loops in the loop region (e.g., two, three, or four loops in LSA or one, two, or three loops in LSA and one loop in LSB).

[098] In certain embodiments, the polypeptide libraries comprise polypeptide members that comprise a C-type lectin domain (CTLD), wherein the CTLD comprises one or more amino acid modifications in at least one of the five loops in the loop region (LSA and LSB), wherein certain Ca 2+ coordinating amino acids in the loop regions are retained. In other embodiments, the polypeptide libraries comprise polypeptide members that comprise a C-type lectin domain (CTLD), wherein the CTLD comprises one or more amino acid modifications in at least one of the five loops in the loop region (LSA and LSB), wherein certain amino acid(s) involved with plasminogen binding activity are eliminated.

[099] In certain embodiments of this aspect, the polypeptide library comprises polypeptide members that comprise a C-type lectin domain (CTLD), wherein the CTLD
comprises one or more amino acid modifications in regions of the CTLD that fall outside of the LSA and LSB
regions. Accordingly, such modifications can be designed or randomly generated in any one or RECTIFIED SHEET (RULE 91) ISA/EP

more of the beta strand and/or alpha helical regions. An example of this is shown in Table 17.
[0100] The loop region of any CTLD, if not already identified or characterized, can be identified by using any variety of structural or sequence-based analysis using the existing sequence based information for any single structurally characterized CTLD or any combination of structurally characterized CTLDs. Typically, the loop regions are stretches of amino acids found between more ordered regions of the CTLD amino acid sequence (e.g., between the a-helices or (3-strands), and typically have a more flexible conformation. Loop segment A
(LSA) in a CTLD
typically falls between the (32 and 133 strands of the canonical CTLD motif.
The (LSA) contains smaller loop regions (loops 1, 2, 3, and 4), which are usually located between small beta sheet structures that provide a degree of order to the (LSA) (see, e.g., FIG 4).
CTLDs typically have a smaller loop structure (loop segment B, "LSB" or "loop 5") located between (33 and (34.

[0101] As mentioned, the loop region of any CTLD can be identified using structural and/or sequence-based analyses based on the existing sequence information for any single structurally characterized CTLD or any combination of structurally characterized CTLDs. For example, the location of the loop region of any uncharacterized CTLD can be identified by aligning a prospective CTLD sequence with the group of structure-characterized CTLDs presented in FIG.
1. The sequence alignments shown in FIG. 1 were strictly elucidated from actual three dimensional structure data. Given that the polypeptide segments of corresponding structural elements of the framework also exhibit strong amino acid sequence similarities, FIG. 1 provides a set of direct sequence-structure signatures, which can readily be inferred from the sequence alignment. As shown in FIG. 1, the loop region (LSA and LSB) is flanked by segments corresponding to the (32-, (33-, and (34-strands (loops 1-4 of LSA typically fall between the (32 and (33 strands of the canonical CTLD and loop 5 of LSB is typically located between [33 and [34 of the CTLD). The (32-, [i3-, and (34-strands can be identified by identification of their respective consensus sequences (published in US Patent Application Publication 2007/0275393). The loop region of the prospective CTLD can be identified by aligning the sequence of the prospective CTLD with the sequence shown in FIG. 1 and assigning approximate locations of framework structural elements as guided by the sequence alignment, i.e., identifying the (32-, (33-, and [34-strands, adjusting the alignment to ensure precise alignment of the four canonical cysteine residues involved in the formation of the two conserved disulfide bridges (Ci-Civ and C11-C111, in RECTIFIED SHEET (RULE 91) ISA/EP

FIG. 1) invariably found in all CTLDs characterized thus far. Furthermore, the loop regions of a prosective CTLD can be identified using known protein structure modeling programs, such as Swiss PDB Viewer DeepView v. 4Ø1 for Macintosh, by aligning the sequence of prospective CTLD with any of the CTLD sequences in FIG 1. Other protein modeling programs that can be used in the same manner are known in the art and available for public use, for example, MODELLER and Selvita SPMP 2.0 (See Sali A, Blundell TL. (1993) Comparative protein modelling by satisfaction of spatial restraints. J. Mol. Biol. 234, 779-815;
Marti-Renom MA, Stuart A, Fiser A, Sanchez R, Melo F, Sali A. (2000) Comparative protein structure modeling of genes and genomes. Annu. Rev. Biophys. Biomol. Struct. 29, 291-325; Fiser A, Sali A. (2003) Modeller: generation and refinement of homology-based protein structure models. Methods Enzymol. 374:461-91).

[0102] The sequence-structure analyses also demonstrate that CTLDs can be used as frameworks in the construction of new classes of CTLD libraries. The additional steps involved in preparing starting materials for the construction of a new class of CTLD library on the basis of a CTLD for which the precise three dimensional structure has not yet been determined includes the following: (1) alignment of the sequence of the new CTLD with the sequence shown in FIG. 1;
and (2) assignment of approximate locations of framework structural elements as guided by the sequence alignment, observing any requirement for minor adjustment of the alignment to ensure precise alignment of the four canonical cysteine residues involved in the formation of the two conserved disulfide bridges (Ci-Civ and C11-C111, in FIG. 1).

[0103] The polypeptides comprising a CTLD used in the polypeptide libraries of the invention can be full-length proteins or partial proteins having a CTLD, for example, the full-length amino acid sequence or partial amino acid sequence of any of the proteins described herein and otherwise known. Alternatively, the polypeptides comprising a CTLD used in the polypeptide libraries of the invention can be polypeptides comprising only CTLD sequence, for example, the amino acid sequence of any of the CTLDs described herein and otherwise known.
The polypeptides comprising CTLD sequence can have additional flanking C-terminal and/or N-terminal (non-CTLD) amino acid sequence.

[0104] In one aspect, the invention provides a combinatorial peptide library, and a library of RECTIFIED SHEET (RULE 91) ISA/EP

nucleic acid sequences encoding the polypeptides of the library, wherein the CTLDs of the polypeptides have been modified according to a number of schemes, which have been labeled for the purposes of identification only as Schemes (a)-(j). While=each scheme is more particularly described herein, the modifications are at least as follows:

[0105] amino acid modifications in at least one of four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise an insertion of at least one amino acid in Loop I and random substitution of at least five amino acids within Loop 1;

[0106] amino acid modifications in at least one of four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise random substitution of at least five amino acids within Loop 1 and random substitution of at least three amino acids within Loop 2;
[0107] amino acid modifications in at least one of four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise random substitution of at least seven amino acids within Loop 1 and at least one amino acid insertion in Loop 4;

[0108] amino acid modifications in at least one of four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise at least one amino acid insertion in Loop 3 and random substitution of at least three amino acids within Loop 3;

[0109] amino acid modifications in at least one of four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise a modification that combines two loops into a single loop, wherein the two combined loops are Loop 3 and Loop 4;

[0110] amino acid modifications in at least one of four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise at least one amino acid insertion in Loop 4 and random substitution of at least three amino acids within Loop 4;

[0111 ] amino acid modifications in at least one of the five loops in loop segment A (LSA) and loop segment B (LSB) of the CTLD, wherein the amino acid modifications comprise random substitution of at least five amino acid residues in Loop 3 and random substitution of at least three amino acids within Loop 5;

[0112] amino acid modifications in at least one of the four loops in loop segment A (LSA) of the RECTIFIED SHEET (RULE 91) ISA/EP

CTLD, wherein the amino acid modifications comprise random substitution of at least one amino acid and insertion of at least six amino acids in Loop 3;

[0113] (i) amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise a mixture of (1) random substitution of at least six amino acids in Loop 3 and (2) random substitution of at least six amino acids and at least one amino acid insertion in Loop 3; and [0114] (j) amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise at least four or more amino acid insertions in at least one of the four loops in the loop segment A (LSA) or loop 5 in loop segment B (LSB) of the CTLD.

[0115] With respect to scheme (a), the invention provides a combinatorial polypeptide library comprising polypeptide members having a randomized C-type lectin domain (CTLD), wherein the randomized CTLD includes amino acid modifications in at least one of the four loops in LSA
or in the loop in LSB of the CTLD, wherein the amino acid modifications comprise at least one amino acid insertion in Loop I and random substitution of at least five amino acids within Loop 1.

[0116] In certain embodiments of this aspect of the combinatorial library, when the CTLD is from human tetranectin, the CTLD also has a random substitution of Arginine-130. For CTLDs other than the CTLD of human tetranectin, this peptide is located immediately adjacent to the C-terminal peptide of Loop 2 in the C-terminal direction. For example, in mouse tetranectin, this peptide is Gly-130. In certain embodiments of this aspect of the combinatorial library, when the CTLD is from tetranectin, for example human or mouse tetranectin, the CTLD
includes a substitution of Lysine- 148 to Alanine in Loop 4.

[0117] In certain embodiments, when the combinatorial library has the modified CTLD of Scheme (a), the amino acid modifications comprise two amino acid insertions in Loop I and random substitution of at least five amino acids within Loop 1. In other embodiments, when the combinatorial library has the modified CTLD of scheme (a) and the CTLD is from human tetranectin, the amino acid modifications comprise at least one amino acid insertion in Loop 1, RECTIFIED SHEET (RULE 91) ISA/EP

random substitution of at least five amino acids within Loop 1, and include a random substitution of Arginine 130. In one specific embodiment, when the combinatorial library has the modified CTLD of scheme (a) and the CTLD is from human tetranectin, the amino acid modifications comprise two amino acid insertions in Loop 1, random substitution of five amino acids within Loop 1, and a random substitution of Arginine 130. In one specific embodiment, when the combinatorial library has the modified CTLD of scheme (a) and the CTLD is from mouse tetranectin, the amino acid modifications comprise two amino acid insertions in Loop 1, random substitution of five amino acids within Loop 1, and a random substitution of Leucine 130. In any of the embodiments for scheme (a), the amino acid modifications can further comprise a substitution of Lysine-148 to Alanine. Thus, in one specific embodiment of this aspect of the combinatorial library, the CTLD comprises two amino acid insertions in Loop 1, random substitution of at least five amino acids within Loop 1, random substitution of Arginine- 130 or other amino acid located outside and adjacent to loop 2 in the C-terminal direction, and a substitution of lysine-148 to alanine in Loop 4.

[0118] With respect to scheme (b), the invention provides a combinatorial polypeptide library comprising polypeptide members having a randomized C-type lectin domain (CTLD), wherein the randomized CTLD comprises amino acid modifications in at least one of the four loops in the LSA of the CTLD, wherein the amino acid modifications comprise random substitution of at least five amino acids within Loop I and random substitution of at least three amino acids within Loop 2.

[0119] In certain embodiments of this aspect of the combinatorial library of scheme (b), when the CTLD is from tetranectin, the amino acid modifications comprise random substitution of at least five amino acids within Loop 1, random substitution of at least three amino acids within Loop 2, and random substitution of Arginine-130, or other amino acid located outside and adjacent to loop 2 in the C-terminal direction. In certain embodiments, when the combinatorial library has the modified CTLD of Scheme (b) and the CTLD is from human tetranectin, the amino acid modifications include random substitutions of at least five amino acids in Loop 1, random substitution of at least three amino acids in Loop 2, and include a random substitution of Arginine 130. In one embodiment, when the combinatorial library has the modified CTLD of Scheme (b) and the CTLD is from human tetranectin, the amino acid modifications include RECTIFIED SHEET (RULE 91) ISA/EP

random substitutions of five amino acids in Loop 1, random substitution of three amino acids in Loop 2, and a random substitution of Arginine 130. In certain other embodiments, when the combinatorial library has the modified CTLD of Scheme (b) and the CTLD is from mouse tetranectin, the amino acid modifications include random substitutions of at least five amino acids in Loop 1, random substitution of at least three amino acids in Loop 2, and include a random substitution of Leucine 130. In one embodiment, when the combinatorial library has the modified CTLD of Scheme (b) and the CTLD is from mouse tetranectin, the amino acid modifications include random substitutions of five amino acids in Loop 1, random substitution of three amino acids in Loop 2, and a random substitution of Leucine 130. In any of the embodiments for scheme (b), the amino acid modifications can further comprise a substitution of Lysine- 148 to Alanine. Thus, in one specific embodiment, the amino acid modifications comprise random substitution of at least five amino acids within Loop 1, random substitution of at least three amino acids within Loop 2, and random substitution of Arginine-130, or other amino acid located outside and adjacent to loop 2 in the C-terminal direction and a substitution of Lysine-148 to Alanine in Loop 4.

[0120] With respect to scheme (c), the invention provides a combinatorial polypeptide library comprising polypeptide members that have a randomized C-type lectin domain (CTLD), wherein the randomized CTLD comprises amino acid modifications in at least one of the four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise random substitution of at least seven amino acids within Loop I and at least one amino acid insertion in Loop 4.

[01211 In certain embodiments of this aspect of the combinatorial library, the polypeptide members of the combinatorial library further comprise random substitution of at least two amino acids within Loop 4. In certain other embodiments of this aspect, the amino acid modifications comprise three amino acid insertions within Loop 4 and optionally further comprise random substitution of at least two amino acids. In one embodiment, the amino acid modifications comprise random substitution of at least seven amino acids within Loop 1, at least three amino acid insertions in Loop 4, and random substitution of at least two amino acids within Loop 4. In one specific embodiment, the amino acid modifications comprise random substitution of seven amino acids within Loop 1, three amino acid insertions in Loop 4, and random substitution of RECTIFIED SHEET (RULE 91) ISA/EP

two amino acids within Loop 4.

[0122] With respect to scheme (d), the invention provides a combinatorial polypeptide library comprising polypeptide members that have a randomized C-type lectin domain (CTLD), wherein the randomized CTLD comprises amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise at least one amino acid insertion in loop 3 and random substitution of at least three amino acids within Loop 3.

[0123] In certain embodiments, when the combinatorial library has the modified CTLD of Scheme (d), the amino acid modifications can further comprise at least one amino acid insertion in Loop 4, and can further comprise random substitution of at least three amino acids within Loop 4. In any of the described embodiments for scheme (d), the amino acid modifications can comprise three amino acid insertions in Loop 3. In any of the described embodiments for scheme (d), the amino acid modifications can comprise three amino acid insertions in Loop 4.
Thus, in certain embodiments, the amino acid modifications comprise random substitution of at least three amino acids within Loop 3, random substitution of at least three amino acids within Loop 4, at least one amino acid insertion in Loop 3 and at least one amino acid insertion in Loop 4. In certain embodiments, the amino acid modifications comprise random substitution of at least three amino acids within Loop 3, random substitution of at least three amino acids within Loop 4, at least three amino acid insertions in Loop 3 and at least three amino acid insertions in Loop 4. In one specific embodiment, the amino acid modifications comprise random substitution of three amino acids within Loop 3, random substitution of three amino acids within Loop 4, three amino acid insertions in Loop 3, and three amino acid insertions in Loop 4. In any of the described embodiments, when the CTLD is tetranectin, the amino acid modifications can further compr random substitution of Lysine-148 to Alanine or in Loop 4.

[0124] With respect to scheme (e), the invention provides a combinatorial polypeptide library comprising polypeptide members that have a randomized C-type lectin domain (CTLD), wherein the randomized CTLD comprises amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise a modification that combines two Loops into a single Loop, wherein the two combined Loops are RECTIFIED SHEET (RULE 91) ISA/EP

Loop 3 and Loop 4. In certain embodiments, when the members of the combinatorial library have the modified CTLD of Scheme (e), the amino acid modifications comprise random substitution of at least six amino acids within Loop 3 and random substitution of at least four amino acids within Loop 4. In one specific embodiment, the amino acid modifications comprise random substitution of six amino acids within Loop 3 and random substitution of four amino .acids within Loop 4. In any of the embodiments for scheme (e), when the CTLD
is from human tetranectin, the amino acid modifications can further comprise random substitution of Proline-144. In one specific embodiment, when the CTLD is from human tetranectin, the amino acid modifications comprise random substitution of six amino acids within Loop 3, random substitution of four amino acids within Loop 4, and a random substitution of proline 144, resulting in a combined Loop 3 and Loop 4 amino acid sequence, comprising, for example, NWEXXXXXXX XGGXXXN (SEQ ID NO: 578), wherein X is any amino acid and wherein the amino acid sequence of SEQ ID NO: 578 forms a single Loop region. Thus, in one specific embodiment, the polypeptide members of the combinatorial library comprise the sequence NWEXXXXXXX XGGXXXN (SEQ ID NO: 578), wherein X is any amino acid and wherein the amino acid sequence of SEQ ID NO: 578 forms a single loop from combined and modified Loop 3 and Loop 4.

[0125] With respect to scheme (f), the invention provides a combinatorial polypeptide library comprising polypeptide members that have a randomized C-type lectin domain (CTLD), wherein the randomized CTLD comprises amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise at least one amino acid insertion in Loop 4 and random substitution of at least three amino acids within Loop 4. In certain embodiments, the amino acid modifications comprise four amino acid insertions in Loop 4. In one embodiment, the amino acid modifications comprise at least four amino acid insertions in Loop 4 and random substitution of at least three amino acids within Loop 4. In one specific embodiment, the amino acid substitutions comprise four amino acid insertions in Loop 4 and random substitution of three amino acids within Loop 4.

[0126] With respect to scheme (g), the polypeptide members of the combinatorial library comprise a modified Loop 3 and a modified Loop 5, wherein the modified Loop 3 comprises randomization of five amino acid residues and the modified Loop 5 comprises randomization of RECTIFIED SHEET (RULE 91) ISA/EP

three amino acid residues. In one embodiment, the polypeptide members of the combinatorial library comprise a modified Loop 3, a modified Loop 5, and a modified Loop 4, wherein the modification to Loop 4 abrogates plasminogen binding. For example, when the combinatorial library has the modified CTLD of Scheme (g), and the CTLD is from tetranectin, the amino acid modifications can further comprise one or more amino acid modifications in Loop 4 that modulates plasminogen binding affinity of the CTLD, for example, the substitution of Lysine 148 to Alanine. Thus, in certain embodiments, when the CTLD is from human or mouse tetranectin, the amino acid modifications comprise random substitution of at least five amino acid residues in Loop 3, random substitution of at least three amino acid residues in Loop 5, and substitution of Lysine 148 to Alanine in Loop 4. In one specific embodiment, the amino acid modifications comprises random substitution of five amino acid residues in Loop 3 and random substitution of three amino acid residues in Loop 5, and, in another specific embodiment, when the CTLD is from human or mouse tetranectin, the amino acid modifications further comprise substitution of Lysine 148 to Alanine in Loop 4.

[0127] With respect to scheme (h), the invention provides a combinatorial polypeptide library comprising polypeptide members that have a randomized C-type lectin domain (CTLD), wherein the randomized CTLD comprises amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the-CTLD, wherein the amino acid modifications comprise random substitution of at least one amino acid and at least six amino acid insertions. In certain embodiments, when the CTLD is from tetranectin, the amino acid modifications can further comprise one or more amino acid modifications in Loop 4 that modulates plasminogen binding affinity of the CTLD, for example, the substitution of lysine 148 to Alanine.
In certain embodiments when the CTLD is from human or mouse tetranectin, the members of the combinatorial library have random substitution of at least one amino acid and insertion of at least six amino acids in Loop 3, and substitution of Lysine 148 to Alanine in Loop 4. In one specific embodiment, the amino acid modifications comprise random substitution of one amino acid and insertion of six amino acids in Loop 3. In one specific embodiment, when the CTLD is from human or mouse tetranectin, the members of the combinatorial library have random substitution of one amino acid and insertion of six amino acids in Loop 3, and substitution of lysine 148 to alanine in Loop 4. In any of these embodiments when the CTLD is from human or mouse tetranectin, one of the substitutions is the substitution of Isoleucine 140.

RECTIFIED SHEET (RULE 91) ISA/EP

[0128] With respect to scheme (i), the invention provides a combinatorial polypeptide library comprising polypeptide members that have a randomized C-type lectin domain (CTLD), wherein the randomized CTLD comprises amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise a mixture of random substitution of six amino acids in Loop 3 and random substitution of six amino acids and one amino acid insertion in Loop 3. In one embodiment, the mixture further comprises random substitution of six amino acids and two amino acid insertions in Loop 3. Thus in one embodiment, the amino acid modifications comprises a mixture of random substitution of six amino acids in Loop 3, random substitution of six amino acids and one amino acid insertion in Loop 3, and random substitution of six amino acids and two amino acid insertions in Loop 3. In any of the embodiments of scheme (i), when the CTLD is from tetranectin, the amino acid modifications further comprise a substitution of Lysine 148 to Alanine in Loop 4.

[0129] With respect to scheme (i), the invention provides a combinatorial polypeptide library comprising polypeptide members that have a randomized C-type lectin domain (CTLD), wherein the randomized CTLD comprises amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise at least four or more amino acid insertions in at least one of the four loops in the loop segment A (LSA) or loop 5 in loop segment B (LSB) of the CTLD.

[0130] In embodiments wherein the combinatorial library comprises one or more amino acid modifications to the Loop 4 region (alone or in combination with modifications to other regions of the CTLD), certain of the modification(s) are designed to maintain, modulate, or abrogate the metal ion-binding affinity of the CTLD. Such modifications affect the plasminogen-binding activity of the CTLD (see, e.g., Nielbo, et al., Biochemistry, 2004, 43 (27), pp 8636-8643; or Graversen 1998).

[0131] The polypeptide members of the libraries can comprise one or more amino acid modifications (e.g., by insertion, substitution, extension, or randomization) in any combination of the four LSA loops and the LSB loop (Loop 5) of the CTLD. Thus, in any of the various embodiments described herein, the randomized CTLD can comprise one or more amino acid RECTIFIED SHEET (RULE 91) ISA/EP

modifications in the loop of the LSB loop region (Loop 5), either alone, or in combination with one or more amino acid modifications in any one, two, three, or four loops of the LSA loop region (Loops 1-4). In one aspect, the invention provides a combinatorial polypeptide library comprising polypeptide members that have a randomized C-type lectin domain (CTLD), wherein the randomized CTLD comprises one or more amino acid modifications in at least one of the four loops in loop segment A (LSA) and one or more amino acid modifications in the loop in loop segment B (LSB) (Loop 5) of the CTLD, wherein the one or more amino acid modifications comprises randomization of the LSB amino acid residues.

[0132] According to the various embodiments described herein, the polypeptide members of the combinatorial libraries can have one or more amino acid modifications in any two, three, four, or five loops in the loop region (LSA and LSB) of the CTLD (e.g., any random combination of random amino acid modifications to two loops, to three loops, to four loops, or to all five loops). The polypeptide members of the combinatorial librar ies can further comprise additional amino acid modifications to regions of the CTLD outside of the loop region (LSA and LSB), such as in the a-helices or R-strands (see, e.g., FIG. 1).

[0133] In further embodiments of the invention, the CTLD loop regions can be extended beyond the exemplary constructs detailed in the non-limiting Examples below.

[0134] In one aspect, the invention also provides a library of nucleic acid molecules encoding polypeptides of the combinatorial polypeptide library according to any one of the above-described aspects and embodiments. In one embodiment of this aspect, the invention provides a library of nucleic acid sequences encoding the polypeptides of the library, wherein the CTLDs of the polypeptides have been modified according to Schemes (a)-(j).

[0135] Generating recombinant CTLD modified loop libraries [0136] In one aspect, the invention provides methods for generating a polypeptide library comprising polypeptide members that have a C-type lectin domain (CTLD), wherein the CTLD
comprises one or more amino acid modifications in at least one of the four loops in loop segment A (LSA) and/or in the loop in loop segment B (LSB) (Loop 5) of the CTLD.

[0137] In embodiments of this aspect, the method comprises generating at least one random RECTIFIED SHEET (RULE 91) ISA/EP

mutation in at least one of the four loops in the LSA region and/or in the loop in the LSB region of the CTLD, wherein the at least one random mutation comprises (a) an insertion of one or more amino acids in the at least one loop; or (b) a substitution of one or more amino acids within or immediately adjacent to the at least one loop; or (c) a deletion of one or more amino acids within or immediately adjacent to the at least one loop; (d) a modification that combines two adjacent loops, or (e) any combination thereof.

[0138] In certain embodiments of this aspect, the method comprises generating random mutations in at least one of the four loops in the LSA region and/or in the loop in the LSB region of the CTLD in accordance with any of Schemes (a)-(j).

[0139] In certain embodiments of this aspect, the polypeptides of the recombinant CTLD
libraries comprise modified CTLDs in which certain Ca 2+ coordinating amino acid(s) in the loop regions is retained and/or comprise modified CTLDs in which plasminogen binding activity is eliminated.

[0140] Also, in certain embodiments of this aspect, the recombinant CTLD
libraries can comprise polypeptides having modified CTLD regions, wherein the amino acid modifications fall outside of the loop region (LSA and LSB) of the CTLD. Accordingly, such modifications can be designed or randomly generated in any one or more of the beta strand and/or alpha helical regions.

[0141] Generating randomized and optimized recombinant CTLD libraries to obtain protein products that can bind specifically to targets of interest can be performed by any technique known in the art such as, for example, oligonucleotide-directed randomization, error-prone PCR
mutagenesis, DNA shuffling by random fragmentation, loop shuffling, loop walking, somatic hypermutation (see, e.g., US Patent Publication 2009/0075378, which is incorporated by reference), and other known methods in the art to create sequence diversity in order to generate molecules with optimal binding activity. (See, e.g., Stemmer, W.P., Proc Natl Acad Sci USA, (Oct. 1994) 91:10747-751; Patrick, W.M. & Firth, A.E., Biomolecular Engineering, (2005) 22:105-112; Firth, A.E. & Patrick, W.M., Bioinformatics, (2005) 21(15):3314-3315; and Lutz S.
& Patrick, W.M., Curr. Opin. Biotechnol., (2004) 15:291-297).

RECTIFIED SHEET (RULE 91) ISA/EP

[0142] In certain embodiments, the generating and optimizing methods comprise an oligonucleotide-directed randomization (NNK or NNS) strategy for mutagenizing the loops. For example, the human tetranectin (hTN) CTLD shown in FIG. 1 and FIG. 4 contains five loops (four loops in LSA and one loop in LSB), which can be altered to confer binding of the CTLD to any target molecule(s) of interest. Random amino acid sequences (generated via randomization, substitution, insertion, etc) can be introduced into one or more of these loops to create libraries from which CTLD domains with the desired binding properties can be selected.
Construction of these libraries containing random peptides constrained within any or all of the five loops of the human tetranectin CTLD can be accomplished using either a NNK or NNS as described herein.
These libraries can comprise further amino acid modifications that are introduced in regions of the CTLD that are outside of the LSA or LSB regions (e.g., the (x-helices and/or a-strands). The following procedure describes a non-limiting, illustrative example of a method by which seven random peptides can be inserted into loop 1 of the hTN CTLD.

[0143] PCR can be used to generate a first fragment (fragment A, see FIG. 7) using the following strategy. Forward oligo 1 Xfor (5'-GG CTG GGC CTG AAC GAC ATG NNK
NNK
NNK NNK NNK NNK NNK TGG GTG GAT ATG ACT GGC GCC-3'; SEQ ID NO: 137) wherein N = A, T, G or C, and K = G or T, encodes the region surrounding loop I of the CTLD, but replaces 15 nucleotides coding for five amino acids (AAEGT; SEQ ID NO:
579) of loop I
with seven NNK codons. These NNK codons encoding seven random amino acids replace the wild type codons encoding the five native tetranectin amino acids. Oligo 1 Xfor (SEQ ID NO:
137) can be annealed with the reverse oligo I Xrev2 (5'-GGC GGT GAT CTC AGT
TTC CCA
OTT CTT GTA GGC GAT GCG GGC GCC AGT CAT ATC CAC CCA-3'; SEQ ID NO: 580).
The two oligos are complementary across 21 nucleotides of their 3' ends.
Referring to Figure 7, PCR is used to generate Fragment A (101 bp) from these two overlapping oligos.
Similarly, a Fragment B (see FIG. 7) can be created by performing PCR using forward oligo BstXl for (5'-ACT GGG AAA CTG AGA TCA CCG CCC AAC CTG ATG GCG GCG CAA CCG AGA
ACT GCG CGG TCC TG-3'; SEQ ID NO: 139) and the reverse primer PstBssRevC (5'-CCC
TGC AGC OCT TGT CGA ACC ACT TGC COT TOG COG CGC CAG ACA GGA CCG CGC
AGT TCT-3'; SEQ ID NO: 140) to generate a 105 bp fragment. PCR can be performed using a high fidelity polymerase or taq blend and standard PCR thermocycling conditions. The 3' end of RECTIFIED SHEET (RULE 91) ISA/EP

fragment A is complementary to the 5' end of fragment B. These fragments can be gel isolated and subsequently combined for overlap extension PCR using outer primers Bglforl2 (SEQ ID
NO: 141) and PstRev (SEQ ID NO: 142). The resulting 195 bp fragment can be gel isolated and then digested with the restriction enzymes Bgl II and Pst I, after which the final 185 bp fragment can be gel isolated and cloned into a phage display vector (such as CANTAB 5E) containing the restriction modified CTLD shown below fused to Gene III, which is similarly digested with Bg1 II and Pst I for cloning.

[0144] Modification of other loops by replacement with randomized amino acids can be similarly performed as described herein. The replacement of defined amino acids within a loop with randomized amino acids is not restricted to any specific loop, nor is it restricted to the original size of the loops. Likewise, total replacement of the loop is not required, partial replacement is possible for any of the loops. In some cases retention of some of the original amino acids within the loop, such as the calcium coordinating amino acids, may be desirable. In these cases, replacement with randomized amino acids may occur for either fewer of the amino acids within the loop to retain the calcium coordinating amino acids, or additional randomized amino acids may be added to the loop to increase the overall size of the loop yet still retain these calcium coordinating amino acids. Very large peptides can be accommodated and tested by combining loop regions, such as loops I and 2 or loops 3 and 4, into one larger replacement loop.
[0145] The nucleic acid molecules can be obtained by ordinary methods for chemical synthesis of nucleic acids by directing the step-wise synthesis to add pre-defined combinations of pure nucleotide monomers or a mixture of any combination of nucleotide monomers at each step in the chemical synthesis of the nucleic acid fragment. In this way it is possible to generate any level of sequence degeneracy, from one unique nucleic acid sequence to the most complex mixture, which will represent a complete or incomplete representation of maximum number unique sequences of 4N, where N is the number of nucleotides in the sequence.

[0146] Complex compositions comprising a plurality of nucleic acid fragments can, alternatively, be prepared by generating mixtures of nucleic acid fragments by chemical, physical or enzymatic fragmentation of high-molecular mass nucleic acid compositions such as, for example, genomic nucleic acids extracted from any organism. To render such mixtures of RECTIFIED SHEET (RULE 91) ISA/EP

nucleic acid fragments useful in the generation of recombinant libraries, as described here, the crude mixtures of fragments, obtained in the initial cleavage step, would typically be size-fractionated to obtain fragments of an approximate molecular mass range which would then typically be adjoined to a suitable pair of linker nucleic acids, designed to facilitate insertion of the linker-embedded mixtures of size-restricted oligonucleotide fragments into the receiving nucleic acid vector.

[0147] Nucleic acid fragments can be inserted in specific locations into receiving nucleic acids by any common method of molecular cloning of nucleic acids, such as by appropriately designed PCR manipulations in which chemically synthesized nucleic acids are copy-edited into the receiving nucleic acid,_in which case no endonuclease restriction sites are required for insertion.
Alternatively, the insertion/excision of nucleic acid fragments may be facilitated by engineering appropriate combinations of endonuclease restriction sites into the target nucleic acid into which suitably designed oligonucleotide fragments may be inserted using standard methods of molecular cloning of nucleic acids.

[0148] After rounds of selection on specific targets (e.g. eukaryotic cells, virus, bacteria, specific proteins, polysaccharides, other polymers, organic compounds etc.) DNA is isolated from the specific phages, and the nucleotide sequence of the segments encoding the ligand-binding region determined, excised from the phagemid DNA and transferred to the appropriate derivative expression vector for heterologous production of the desired product.
Heterologous production in a prokaryote can be used for the isolation of the desired product.

[0149] To facilitate the construction of combinatorial CTLD libraries, restriction sites can be introduced into the CTLD. For example, suitable restriction sites located in the vicinity of the nucleic acid sequences encoding (32, [33 and [34 in both human and murine tetranectin were designed with minimal perturbation of the polypeptide sequence encoded by the altered sequences. It was found possible to establish a design strategy, as detailed below, by which identical endonuclease restriction sites could be introduced at corresponding locations in the two sequences, allowing interesting loop-region variants to be readily excised from a recombinant murine CTLD and inserted correctly into the CTLD framework of human tetranectin or vice versa.

RECTIFIED SHEET (RULE 91) ISA/EP

[0150] Analysis of the nucleotide sequence encoding the mature form of human tetranectin (FIG.
2) reveals that a recognition site for the restriction endonuclease Bgl II is found at position 326 to 331 (AGATCT), involving the encoded residues Glul 09, Ilel 10, and Trpl I I of 02, and that a recognition site for the restriction endonuclease Kas I is found at position 382 to 387 (GGCGCC), involving the encoded amino acid residues G1y128 and A1a129 (located C-terminally in loop 2). By utilizing alternate codons for naturally occurring amino acids in the tetranectin sequence, the restriction endonuclease sites Pst I (CTGCAG) and Mfe I (CAATTG) were engineered into the tetranectin coding sequence at positions 501 to 506 (CTGCCG, originally), involving the encoded amino acid residues Arg167, Cys168, and Arg169, and positions 511 to 516 (CAGCTG, originally), involving the encoded amino acid residues Gln171 and Leu172, all located between 04 and 05.

[0151 ] In certain other aspects of the invention, nucleic acid constructs in the form of plasmids, vectors, transcription or expression cassettes which comprise at least one nucleic acid described herein are provided. Suitable vectors can be chosen or constructed, containing appropriate regulatory sequences, including promoter sequences, terminator sequences, polyadenylation sequences, enhancer sequences, marker genes and other sequences as appropriate. Vectors may be plasmids, viral e.g. phage, or phagemid, as appropriate. For further details see, for example, Molecular Cloning: a Laboratory Manual: 2nd edition, Sambrook et al., 1989, Cold Spring Harbor Laboratory Press.

[0152] The invention also provides a recombinant host cell which comprises one or more of the constructs as described herein. Suitable host cells include bacteria, mammalian cells, yeast, and baculovirus systems. Mammalian cell lines available in the art for expression of a heterologous polypeptide include Chinese hamster ovary cells, HeLa cells, baby hamster kidney cells, NSO
mouse melanoma cells and many others. In one embodiment the host cell is HEK293 cells.
[0153] Display Systems [0154] The resulting recombinant CTLD libraries described herein can be displayed using a number of alternative techniques that are described herein and known in the art. Methods for expressing the nucleic acid molecule library in a display system are described in US Patent Application Publication 2007/0275393, which is incorporated by reference herein in its entirety.

RECTIFIED SHEET (RULE 91) ISA/EP

In one embodiment, the display system comprises an observable phenotype that represents at least one property of the displayed expression products and the corresponding genotypes.
Examples of suitable display systems include a phage display system; a yeast display system; a viral display system; a cell-based display system; a ribosome-linked display system; or a plasmid-linked display system; any combinations thereof, or any other suitable display system that is known in the art.

[0155] Thus, in one aspect, the invention provides a display system comprising the combinatorial polypeptide library according to any one of the above-described aspects and embodiments. In one embodiment of this aspect, the invention provides a display system comprising the combinatorial polypeptide library according to Schemes (a)-(i).

[0156] In certain embodiments of this aspect, the display system comprises a phage display system; a yeast display system; a viral display system; a cell-based display system; a ribosome-linked display system; or a plasmid-linked display system; any combinations thereof, or any other display system that is known in the art.

[0157] Several systems displaying phenotype, in terms of putative ligand binding modules or modules with putative enzymatic activity, have been described. These include:
phage display (e.g., the filamentous phage fd (Dunn (1996); Griffiths and Duncan (1998);
Marks et al. (1992)), phage lambda display (Mikawa et al. (1996)), display on eukaryotic virus (e.g., baculovirus (Ernst et al. (2000))), cell display (e.g., display on bacterial cells (Benhar et al. (2000))), yeast cells (Boder and Wittrup (1997)), and mammalian cells (Whitehorn et al.
(1995)), ribosome linked display (Schaffitzel et al. (1999)), and plasmid linked display (Gates et al. (1996)).

[0158] A commonly used method for phenotype display and linking this to genotype is by phage display. This is accomplished by insertion of the reading frame encoding the scaffold protein or protein of interest to a surface exposed phage protein. The filamentous phage fd (e.g. M13) has proven useful for this purpose.

[0159] US Patent Application Publication No: 2007/0275393 describes a procedure for accomplishing a display system for the generation of CTLD libraries. In general, a method for generating a display system for the described CTLD libraries comprises:

RECTIFIED SHEET (RULE 91) ISA/EP

[0160] (1) identifying the location of the loop-region of a CTLD;

[0161 ] (2) subcloning a nucleic acid fragment encoding the CTLD of choice into a protein display vector system with or without prior insertion of endonuclease restriction sites close to the sequences encoding (i2, (33 and (34 in the CTLD; and [0162] (3) substituting the nucleic acid fragment encoding some or all of the loop-region of the CTLD of choice with randomly selected members of an ensemble consisting of a multitude of nucleic acid fragments, resulting in randomization and/or extension of the original loop region of the CTLD. Each of the cloned nucleic acid fragments, encoding a new polypeptide with a substituted loop segment or entire loop region, will be decoded in the reading frame determined within its new sequence context.

[0163] The location of the loop region of a CTLD can be identified using the methods previously described herein. Briefly, the loop region can be identified by referring to the three dimensional structure of the CTLD of choice, if such information is available, or, if not, identifying the sequence locations of the (32-, (33- and (34-strands by sequence alignment with the sequences shown in FIG. 1, as aided by the identification of sequence elements corresponding to the (32 and (33 consensus sequence elements and (34-strand characteristics, and the conserved cysteine residues also disclosed herein in FIG. 1.

[0164] Strategies for Identifying and Isolating CTLD polypeptides that bind to target molecules [0165] In one aspect, the invention provides a method for identifying and isolating a polypeptide having specific binding activity to a target molecule, wherein the method comprises (a) providing a combinatorial polypeptide library of the invention; (b) contacting the polypeptides of the combinatorial polypeptide library with the target molecule under conditions that allow for binding between a polypeptide and the target molecule; and (c) isolating a polypeptide that binds to the target molecule. In various embodiments, the target molecule can comprise any molecule associated with the surface of a cell (such as eukaryotic cells, tumor cells, immune cells, bacterial cells, protozoa, fungi and a cell infected with a virus); proteins (such as receptor proteins, soluble proteins, enzymes, or antibodies); polysaccharides;
polymers; and small organic compounds.

RECTIFIED SHEET (RULE 91) ISA/EP

[0166] In another aspect, the invention provides a method for identifying and isolating a polypeptide having specific binding activity to a target molecule, wherein the method further comprises a library of nucleic acid molecules encoding polypeptides of the combinatorial polypeptide library, wherein the library of nucleic acids is expressed in a display system. In one embodiment, the display system comprises an observable phenotype that represents at least one property of the displayed expression products and the corresponding genotypes.

[0167] In another aspect, the invention provides a method for identifying and isolating a polypeptide having specific binding activity to a target molecule comprising the steps of: (a) providing a library of nucleic acid molecules encoding the polypeptide library of claim 1; (b) expressing the library of nucleic acid molecules in a display system to obtain an ensemble of polypeptides, in which the amino acid residues at one or more sequence positions differ between different members of said ensemble of polypeptides; (c) contacting the ensemble of polypeptides with said target molecule under conditions that allow for binding between a polypeptide and the target molecule; and (d) isolating a polypeptide that is capable of binding to said target molecule.
[0168] In any of these aspects and embodiments, the invention provides a method for identifying and isolating a polypeptide having specific binding activity to a target molecule, wherein the polypeptide has been modified in accordance with any of Schemes (a)-(i).

[0169] A specific binding member for a target molecule of interest can be obtained from a random library of polypeptides by selection of members of the library that specifically bind to the target molecule. As discussed herein, a number of systems for displaying phenotypes with putative ligand binding sites are known. These include: phage display (e.g.
the filamentous phage fd [Dunn (1996), Griffiths and Duncan (1998), Marks et al. (1992)], phage lambda [Mikawa et al. (1996)]), display on eukaryotic virus (e.g. baculovirus [Ernst et al. (2000)]), cell display (e.g. display on bacterial cells [Benhar et al. (2000)], yeast cells [Boder and Wittrup (1997)], and mammalian cells [Whitehorn et al. (1995)], ribosome linked display [Schaffitzel et al. (1999)], and plasmid linked display [Gates et al. (1996)].

[0170] To select for polypeptides with binding activity to a target molecule, libraries can be constructed and initially screened for binding to the target molecule as monomeric elements, either as single monomeric CTLD domains or individual peptides displayed on the surface of RECTIFIED SHEET (RULE 91) ISA/EP

phage. Libraries can be constructed by randomizing the amino acids in one or more of the five different loops (or outside the loops) within the CTLD scaffold displayed on the surface of phage. Binding to the target molecules can be selected for by phage display panning.

[0171 ] Several strategies can be employed in the construction of phage display libraries. One strategy is to construct and/or use random peptide phage display libraries.
Random linear peptides and/or random peptides constructed as disulfide constrained loops can be individually displayed on the surface of phage particles and selected for binding to the desired target molecule through phage display "panning". After obtaining peptide clones with the desired binding activity, these peptides can be grafted on to the trimerization domain of human tetranectin or into loops of the CTLD domain followed by grafting on the trimerization domain and screened for agonist activity.

[0172] Another strategy for construction of phage display libraries and trimerization domain constructs include obtaining CTLD derived binders. Libraries can be constructed by randomizing the amino acids in one or more of the five different loops within the CTLD scaffold (i.e., of human tetranectin) displayed on the surface of phage. Binding to the target molecule can be selected for through phage display panning. After obtaining CTLD clones with peptide loops demonstrating the desired binding activity, the CTLD clones can then be grafted on to the trimerization domain of human tetranectin and screened for agonist activity.

[0173] Another strategy includes using peptide sequences with known binding capabilities to the target of interest and first improving their binding by creating new libraries with randomized amino acids flanking the peptide or/and randomized selected internal amino acids within the peptide, followed by selection for improved binding through phage display.
After obtaining binders with improved affinity, the binders of these peptides can be fused to other functional protein domains such as, for example, the trimerization domain of human tetranectin (discussed herein below and discussed in detail in PCT/US09/60271 and US. 2010/0028995, which are incorporated herein by reference in their entirety), and evaluated for desired activity. In this method, initial libraries can be constructed as either free peptides displayed on the surface of phage particles, as in the first strategy, or as constrained loops within the CTLD scaffold as in the second strategy discussed above. These display strategies are described in detail in RECTIFIED SHEET (RULE 91) ISA/EP

PCT/US09/60271, which is incorporated by reference herein in its entirety.

[0174] Exemplary strategies for identifying and isolating polypeptides having specific binding activity with a target molecule of interest are described in further detail below. Although these strategies focus on phage display, other equivalent methods of identifying polypeptides can be used.

[0175] Strategy 1 [0176] Peptide display library kits such as, but not limited to, the New England Biolabs Ph.D.
Phage display Peptide Library Kits are sold commercially and can be purchased for use in selection of new and novel peptides with specific binding activity for a target molecule of interest. Three forms of the New England Biolabs kit are available: the Ph.D.-7 Peptide Library Kit containing linear random peptides 7 amino acids in length, with a library size of 2.8x109 independent clones, the Ph.D.-C7C Disulfide Constrained Peptide Library Kit containing peptides constructed as disulfide constrained loops with random peptides 7 amino acids in length and a library size of 1.2x109 independent clones, and the Ph.D.-12 Peptide Library Kit containing linear random peptides 12 amino acids in length, with a library size of 2.8x 109 independent clones.

[0177] Alternatively similar libraries can be constructed de novo with peptides containing random amino acids similar to these kits. For de novo construction, random nucleotides can be generated using either an NNK, or NNS strategy, in which N represents an equal mixture of the four nucleic acid bases A, C, G and T. The K represents an equal mixture of either G or T, and S
represents and equal mixture of either G or C. These randomized positions can be cloned onto the Gene III protein in either a phage or phagemid display vector system. Both the NNK and the NNS strategy cover all 20 possible amino acids and one stop codon with slightly different frequencies for the encoded amino acids. Because of the limitations of bacterial transformation efficiency, library sizes generated for phage display are in the order of those started above, thus peptides containing up to 7 randomized amino acids positions can be generated and yet cover the entire repertoire of theoretical combinations (207=1.28x109). Longer peptide libraries can be constructed using either the NNK or NNS strategy however the actual phage display library size likely will not cover all the theoretical amino acid combinations possible associated with such RECTIFIED SHEET (RULE 91) ISA/EP

lengths due to the requirement for bacterial transformation.

[0178] Thus ribosome display libraries might be beneficial where larger/
longer random peptides are involved. For disulfide constrained libraries, a similar NNK or NNS random nucleotide strategy can be used. However, these random positions are flanked by cysteine amino acid residues, to allow for disulfide bridge formation. The N-terminal cysteine is often preceded by an additional amino acid such as alanine. In addition a flexible linker made up of but not limited to several glycine residues may act as a spacer between the peptides and the gene III protein for any of the above random peptide libraries.

[0179] Strategy 2 [0180] The human tetranectin CTLD shown in FIGs. 1 and 4 contains five loops (four loops in LSA and one loop comprising LSB), which can be altered to confer binding of the CTLD to different protein targets. Random amino acid sequences can be placed in one or more of these loops to create libraries from which CTLD domains with the desired binding properties can be selected. For example, any of the CTLD polypeptide libraries described herein can be used, i.e., polypeptides having CTLDs modified in accordance with any of Schemes (a)-(i).
Construction these libraries containing random peptides constrained within any or all of the five loops of the human tetranectin CTLD can be accomplished (but is not limited to) using either a NNK or NNS
as described above in strategy I and also described in detail elsewhere herein.

[0181 ] Strategy 3 [0182] In instances where other peptides with binding activity to the target molecule of interest have been identified, a strategy can be utilized in which these peptides can be cloned directly on to either the N- or C- terminal end of the trimerization domain of tetranectin as free linear peptides or as disulfide constrained loops using cysteines can be utilized.
Single-chain antibodies or domain antibodies capable of binding to the target of interest can also be cloned on to either end of the trimerization domain. Additionally, peptides with known binding properties can be cloned directly into any one of the loop regions of the TN CTLD. Peptides selected as disulfide constrained loops or as complementarity-determining regions of antibodies might be quite amenable to relocation into the loop regions of the CTLD of human tetranectin.
Binding can be RECTIFIED SHEET (RULE 91) ISA/EP

tested for all of these constructs in monomeric form, and binding and agonist activation can be tested in trimeric form, when the CTLD is fused with the trimerization domain [0183] CTLD Polypeptides [0184] The combinatorial polypeptide libraries of the invention can be used to generate and identify polypeptides comprising CTLDs with desired binding properties to target molecules of interest.

[0185] In one aspect, the invention provides a polypeptide having the scaffold structure of a C-type Lectin Like Domain (CTLD), wherein the polypeptide binds to a target other than a natural target for that CTLD and wherein the CTLD scaffold structure of the CTLD is modified according to any of the schemes (a) - (j). In one embodiment, the CTLD
scaffold structure is modified according to any of the schemes (a) - (j) and further comprises any of the further modifications described herein, for example, modifications outside the CTLD
loop region. In one embodiment, the polypeptide has the scaffold structure of the CTLD from human or mouse tetranectin and binds to a target other than plasminogen.

[0186] The CTLD polypeptide of the invention can be produced using any of the methods and combinatorial libraries described herein. For example, in one embodiment, the polypeptide can be produced using a combinatorial library of polypeptides having a CTLD, wherein the loop region of the CTLD is randomized according to any of the Schemes (a) - (j), contacting the combinatorial polypeptide library with the target molecule under conditions that allow for binding between a polypeptide and the target molecule; and isolating a polypeptide that binds to the target molecule, wherein the the target molecule is not the natural target for that CTLD. In one embodiment of this method, the CTLD is human or mouse tetranectin. In another embodiment of this method, the CTLD is randomized according to any of the Schemes (a) - (j) and comprises any of the further modifications described herein, for example, modifications outside the CTLD loop region.

[0187] A non-natural target for a modified CTLD according to, the invention can be any chemical compound in free or conjugated form which exhibits features of an immunological hapten, a hormone such as steroid hormones, or any biopolymer or fragment thereof, for RECTIFIED SHEET (RULE 91) ISA/EP

example, a protein or protein domain; a peptide; an oligodeoxynucleotide; a nucleic acid;
arachidonic acid or its metabolites, lipids or metabolites thereof; fatty acids or metabolites thereof; free radicals; an oligo- or polysaccharide or conjugates thereof; or chemically synthesized or natural drugs of abuse or therapeutic use. In one aspect, the target is a protein.
The protein can be any globular soluble protein or a receptor protein, for example, a trans-membrane protein involved in cell signaling, a component of the immune systems such as an MHC molecule or cell surface receptor that is indicative of a specific disease. The protein can be a post translationally modified protein having the addition of a biochemical functional group such as acetate, phosphate,and/or various lipids and carbohydrates, including but not limited to, glycosylation and myristoylation. The modified CTLD of the invention can also bind protein fragments. For example, the CTLD can bind to a domain of a cell surface receptor, when it is part of the receptor anchored in the cell membrane as well as to the same domain in solution, if this domain can be produced as a soluble protein as well. The CTLDs can also have specific binding affinity to ligands of low(er) molecular weight such as biotin, fluorescein or digoxigenin.
[0188] In various embodiments, the CTLD polypeptide sequences that bind one or more target molecule(s) can have binding affinities that are about equal to the binding affinities of naturally occurring ligands for the one or more target molecule(s). In certain embodiments, the polypeptides of the invention have a binding affinity for one or more target molecule(s) that is stronger than the binding affinity that a native ligand has for the same target molecule(s). Such polypeptides are useful, for example, for blocking the activity of binding members in some cases, or for more potently agonizing in other cases, e.g., in cases in which the modified CTLD
binds to a receptor and is further selected to agonize the receptor. In other embodiments, the polypeptides of the invention have a binding affinity for one or more target molecule(s) that is weaker than the binding affinity that a native ligand has for the same target molecule(s). CTLD
polypeptides having a weaker affinity for a target molecule(s) than a native ligand may have an improved ability to penetrate tumors or tissues and/or may be useful in cases where the desired goal is to dampen the activity of the target rather than completely block it.
CTLDs with a lower binding affinity over a native ligand could also be desired, for example, in cases where the optimal selected activity is based on internalization into the cell following binding to the target.
[0189] The modified CTLDs can also bind to one or more receptor(s) and act as agonists. In RECTIFIED SHEET (RULE 91) ISA/EP

such embodiments, the respective binding affinity of the agonists can be determined and compared to the binding properties of native ligands, or a portion thereof, by ELISA, RIA, and/or BlAcore assays, as well as other assays known in the art. In certain embodiments, the receptor-selective agonists of the invention inhibit or induce a biological activity in at least one type of mammalian cell (e.g., a cancer cell), and such activity can be determined by known art methods. Examples of CTLDs identified using the methods provided herein that act as agonists are polypeptides that bind to TRAIL-RI and TRAIL-R2.

[0190] In other embodiments, the modified CTLDs can bind to one or more receptor(s) or one or more ligand(s) having affinity for a receptor(s) and act as antagonists (receptor blockers). In such embodiments, the respective binding affinity of the agonists can be determined and compared to the binding properties of native ligands, or a portion thereof, by ELISA, RIA, and/or BIAcore assays, as well as other assays known in the art. In certain embodiments, the antagonists of the invention inhibit or induce a biological activity in at least one type of mammalian cell (e.g., a cancer cell), and such activity can be determined by known art methods.
Examples of CTLDs identified using the methods provided herein that act as antagonists are polypeptides that bind to IL-23R.

[0191] Polypeptides comprising CTLDs that specifically bind to a target molecule of interest can comprise a "binding member", which includes all or a portion of the CTLD. The term "binding member" as used herein refers to a member of a pair of molecules which have binding specificity for one another. The members of a binding pair may be naturally derived or wholly or partially synthetically produced. One member of the pair of molecules has an area on its surface, or a cavity, which binds to and is therefore complementary to a particular spatial and polar organization of the other member of the pair of molecules. Thus the members of the pair have the property of binding specifically to each other.

[0192] In embodiments wherein the CTLD-based protein products are derived from a mammalian tetranectin, as exemplified herein with murine and human tetranectin, the structure is nearly identical with all other mammalian tetranectins. This species-conserved structure allows for straightforward swapping of polypeptide segments defining ligand-binding specificity between orthologs (e.g. murine and human tetranectin derivatives). Thus, in such embodiments, RECTIFIED SHEET (RULE 91) ISA/EP

this platform provides a particular advantage over the "humanization" of murine antibody derivatives, which can involve a number of complications.

[0193] In one aspect, the invention provides a polypeptide having a multimerizing domain and comprises at least one CTLD polypeptide-binding member that binds to at least one target molecule. As used herein, the term "multimerizing domain" means an amino acid sequence that comprises the functionality that can associate with two or more other amino acid sequences to form trimers or other multimeric complexes. In various embodiment so of the invention, the multimerizing domain is a dimerizing domain, a trimerizing domain, a tetramerizing domain, a pentamerizing domain, etc. These domains are capable of forming polypeptide complexes of two, three, four, five or more polypeptides of the invention.

[0194] In one example, the polypeptide contains an amino acid sequence - a "trimerizing domain" -- which forms a trimeric complex with two other trimerizing domains.
A trimerizing domain can associate with other trimerizing domains of identical amino acid sequence (forming a homotrimer), or with trimerizing domains of different amino acid sequence (forming a heterotrimer). The interaction is of the type that produces trimeric proteins or polypeptides. Such an interaction may be caused by covalent bonds between the components of the trimerizing domains as well as by hydrogen bond forces, hydrophobic forces, van der Waals forces and salt bridges. The trimerizing effect of trimerizing domain is caused by a coiled coil structure that interacts with the coiled coil structure of two other trimerizing domains to form a triple alpha helical coiled coil trimer that is stable even at relatively high temperatures. In various embodiments, for example, a trimerizing domain based upon a tetranectin structural element, the complex is stable at least 60 C, for example in some embodiments at least 70 C.

[01951 In one embodiment, the multimerized polypeptide is a trimer, for example a tetranectin trimerizing module (see US 2007/0154901). A trimeric complex including a CTLD
is referred to herein as an "atrimer." An "ATRIMERTM" polypeptide complex refers to a trimeric complex of three trimerizing domains that also include CLTDs (Anaphore, Inc., San Diego, California).
[0196] In accordance with the invention, a binding member may either be linked to the N- or the C-terminal amino acid residue of the multimerizing domain. Also, in certain embodiments it may be advantageous to have a binding member at both the N-terminus and the C-terminus of RECTIFIED SHEET (RULE 91) ISA/EP

the multimerizing domain of the monomer, thereby providing a multimeric polypeptide complex.
For example, when the multimeric peptide forms trimers with like molecules, six binding members capable of binding a target molecule of interest can be associated with a single trimeric complex.

[0197] In another aspect of the invention, a polypeptide that specifically binds to a target molecule of interest is contained in one or more loops in the loop region of a CTLD. In this aspect, the CTLD can be attached to any known trimerizing domain at the C-terminus of the trimerizing domain. Also, a fusion protein of the invention can include a second CTLD domain, fused at the N-terminus of the trimerizing domain. In a variation of this aspect, the fusion protein includes a polypeptide that binds to a first target molecule at one of the termini of the trimerizing domain and a CTLD at the other of the termini. One, two or three such proteins can be part of a trimeric complex containing up to six specific CTLD binding members for one or more target molecules.

[0198] In another aspect, the invention provides a multimeric complex of three proteins, each of the proteins comprising a multimerizing domain and at least one CTLD
polypeptide that binds to at least one target molecule of interest. In one embodiment, the multimeric complex comprises a fusion protein having a multimerizing domain selected from a tetranectin trimerizing structural element (tetranectin trimerizing module), a mannose binding protein (MBP) trimerizing domain, a collectin neck region, and other similar moieties. The multimeric complex can be comprised of multimerizing domains that are able to associate with each other to form a multimer.
Accordingly, in certain embodiments, the multimeric complex is a homomultimeric complex comprised of proteins having the same amino acid sequences. In other embodiments, the multimeric complex is a heteromultimeric complex comprised of proteins having different amino acid sequences such as, for example, different multimerizing domains, and/or different CTLD
polypeptides that bind to a different target molecule. In such embodiments, the CTLD
polypeptides may all specifically bind to one target molecule. In other embodiments, the CTLD
polypeptides specifically bind to different target molecules. Thus, in certain embodiments, the multimeric complex comprises fusion proteins of the invention, wherein each of the fusion proteins comprise at least one CTLD polypeptide that binds to one target molecule, wherein the polypeptides can be the same or different, and/or at least one CTLD
polypeptide that binds to a RECTIFIED SHEET (RULE 91) ISA/EP

second target molecule, wherein the second target molecule-binding polypeptide can be the same or different.

[0199] The trimerizing domain of a polypeptide of the invention can be derived from tetranectin as described in U.S. Patent Application Publication No. 2007/0154901 ('901 Application), which is incorporated by reference in its entirety. The mature human tetranectin single chain polypeptide sequence is provided herein as SEQ ID NO: 11. Examples of a tetranectin trimerizing domain include the amino acids 17 to 49, 17 to 50, 17 to 51 and 17-52 of SEQ ID
NO: 40, which represent the amino acids encoded by exon 2 of the human tetranectin gene, and optionally the first one, two or three amino acids encoded by exon 3 of the gene. Other examples include amino acids I to 49, 1 to 50, 1 to 51 and I to 52, which represents all of exons I and 2, and optionally the first one, two or three amino acids encoded by exon 3 of the gene.
Alternatively, only a part of the amino acid sequence encoded by exon 1 is included in the trimerizing domain. In particular, the N-terminus of the trimerizing domain may begin at any of residues 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16 and 17 of SEQ
ID NO: 40. In particular embodiments, the N terminus is 110 or VI 7 and the C-terminus is Q47, T48, V49, C(S)50, L51 or K52 (numbering according to SEQ ID NO: 40). See PCT US09/60271, which is incorporated by reference herein in its entirety.

[0200] The trimerizing domain can be a tetranectin trimerizing structural element ("TTSE") having an amino acid sequence of SEQ ID NO: 40 which is a consensus sequence of the tetranectin family trimerizing structural element as more fully described in US 2007/00154901, which is incorporated herein by reference in its entirety. The TTSE embraces variants of a naturally occurring member of the tetranectin family of proteins, and in particular variants that have been modified in the amino acid sequence without adversely affecting, to any substantial degree, the ability of the TTSE to form alpha helical coiled coil trimers. In various aspects of the invention, the trimeric polypeptide according to the invention includes a TTSE
as a trimerizing domain having at least 66% amino acid sequence identity to the consensus sequence of SEQ ID
NO: 49; for example at least 73%, at least 80%, at least 86% or at least 92%
sequence identity to the consensus sequence of SEQ ID NO: 40 (counting only the defined (not X) residues). In other words, at least one, at least two, at least three, at least four, or at least five of the defined amino acids in SEQ ID NO: 40 may be substituted.

RECTIFIED SHEET (RULE 91) ISA/EP

[0201) In one particular embodiment, the cysteine at position 50 (C50) of SEQ
ID NO: 40 can be advantageously mutagenized to serine, threonine, methionine or to any other amino acid residue in order to avoid formation of an unwanted inter-chain disulphide bridge, which can lead to unwanted multimerization. Other known variants include at least one amino acid residue selected from amino acid residue nos. 6, 21, 22, 24, 25, 27, 28, 31, 32, 35, 39, 41, and 42 (numbering according to SEQ ID NO: 40), which may be substituted by any non-helix breaking amino acid residue. These residues have been shown not to be directly involved in the intermolecular interactions that stabilize the trimeric complex between three TTSEs of native tetranectin monomers. In one aspect shown in FIG. 2, the TTSE has a repeated heptad having the formula a-b-c-d-e-f-g (N to C), wherein residues a and d (i.e., positions 26, 30, 33, 37, 40, 44, 47, and 51 may be any hydrophobic amino acid (numbering according to SEQ ID
NO: 40).
[0202] In further embodiments, the TTSE trimerization domain can be modified by the incorporation of polyhistidine sequence and/or a protease cleavage site, e.g, Blood Coagulating Factor Xa or Granzyme B (see US 2005/0199251, which is incorporated herein by reference), and by including a C-terminal KG or KGS sequence. Also, to assist in purification, Proline at position 2 may be substituted with Glycine.

[0203) Particular non-limiting examples of TTSE truncations and variants are shown in PCT
US09/60271 (FIGs 3A-3D). In addition, a number of trimerizing domains having substantial homology (greater than 66 %) to the trimerizing domain of human tetranectin known:

Table 1- Trimerizing Domains Equus caballus TN-like KMFEELKSQLDSLAQEVALLKEQQALQTVCL SEQ ID NO: 66 Cat TN KMFEELKTQVDSLAQEVALLKEQQALQTVCL SEQ ID NO: 67 Mouse TN SKMFEELKNRMDVLAQEVALLKEKQALQTVCL SEQ ID NO: 68 Rat TN KMFEELKNRLDVLAQEVALLKEKQALQTVCL SEQ ID NO: 69 Bovine TN KMLEELKTQLDSLAQEVALLKEQQALQTVCL SEQ ID NO: 70 Equus caballus CTLD DLKTQVEKLWREVNALKEMQALQTVCL SEQ ID NO: 71 like Canis lupus CTLD DLKTQVEKLWREVNALKEMQALQTVCL SEQ ID NO: 72 member A
Bovine CTLD member A DLKTQVEKLWREVNALKEMQALQTVCL SEQ ID NO: 73 RECTIFIED SHEET (RULE 91) ISA/EP

Macaca mulatta CTLD DLKTQVEKLWTEVNALKEMQALQTVCL SEQ ID NO: 74 member A
Taeniopygia guttata DDLKTQIDKLWREVNALKEMQALQTVCL SEQ ID NO: 75 CTLD member A
Ornithorhynchus DLKTQVEKLWREVNALKEMQALQTVCL SEQ ID NO: 76 anatinus CTLD like Rat CTLD member A DLKSQVEKLWREVNALKEMQALQTVCL SEQ ID NO: 77 Monodelphis domestics DLKTQVEKLWREVNALKEMQALQTVCL SEQ ID NO: 78 CTLD member A
Shark TN DDLRNEIDKLWREVNSLKEMQALQTVCL SEQ ID NO: 79 Taeniopygia guttata KMIEDLKAMIDNISQEVALLKEKQALQTVCL SEQ ID NO: 80 TN-like Gallus gallus TN KMIEDLKAMIDNISQEVALLKEKQALQTVCL SEQ ID NO: 81 Danio rerio CTLD DDMKTQIDKLWQEVNSLKEMQALQTVCL SEQ ID NO: 82 member A
Gallus gallus, CTLD DDLKTQIDKLWREVNALKEMQALQSVCL SEQ ID NO: 83 member A
Mouse CTLD member A DDLKSQVEKLWREVNALKEMQALQTVCL SEQ ID NO: 84 Gallus gallus CTLD DDLKTQIDKLWREVNALKEMQALQSVCL SEQ ID NO: 85 member A
SEQ ID NO: 86 Tetraodon DDVRSQIEKLWQEVNSLKEMQALQTVCL
nigroviridis, unkown Xenopus laevis DLKTQIDKLWREINSLKEMQALQTVCL SEQ ID NO: 87 Tetraodon EELRRQVSDLAQELNILKEQQALHTVCL SEQ ID NO: 88 nigroviridis, unkown Xenopus laevis,unkown KMYEELKQKVQNIELEVIHLKEQQALQTICL SEQ ID NO: 89 Xenopus tropicalis TN KMYEDLKKKVQNIEEDVIHLKEQQALQTICL SEQ ID NO: 90 Salmo salar TN EELKKQIDNIVLELNLLKEQQALQSVCL SEQ ID NO: 91 Danio rerio TN EELKKQIDQIIQDLNLLKEQQALQTVCL SEQ ID NO: 92 Tetraodon EQMQKQINDIVQELNLLKEQQALQAVCL SEQ ID NO: 93 nigroviridis, unknown Tetraodon EQMQKQINDIVQELNLLKEQQALQAVCL SEQ ID NO: 94 nigroviridis, unkown [0204] Other human polypeptides that are known to trimerize include those found in Table 2.
[0205] Table 2- Trimerizing Polypeptides hTRAF3 NTGLLESQLSRHDQMLSVHDIRLADMDLRFQVLETASYNG SEQ ID NO: 95 VLIWKIRDYKRRKQEAVM
EhNBP AASERKALQTEMARIKKWLTF SEQ ID NO: 96 RECTIFIED SHEET (RULE 91) ISA/EP

hSPC300 FDMSCRSRLATLNEKLTALERRIEYIEARVTKGETLT SEQ ID NO: 97 hNEMO ADIYKADFQAERQAREKLAEKKELLQEQLEQLQREYSKLK SEQ ID NO: 98 ASCQESARI
hcubilin LTGSAQNIEFRTGSLGKIKLNDEDLSECLHQIQKNKEDII SEQ ID NO: 99 ELKGSAIGLPIYQLNSKLVDLERKFQGLQQT
hThrombos LRGLRTIVTTLQDSIRKVTEENKELANE SEQ ID NO: 100 pondins [0206] Another example of a trimerizing domain is disclosed in US 6,190,886 (incorporated by reference herein in its entirety), which describes polypeptides comprising a collectin neck region.
Trimers can then be made under appropriate conditions with three polypeptides comprising the collectin neck region amino acid sequence. A number of collectins are identified, including:
[0207] Collectin neck region of human SP-D:

VASLRQQVEALQGQVQHLQAAFSQYKK [SEQ ID NO: 101]
[0208] Collectin neck region of bovine SP-D:
VNALRQRVGILEGQLQRLQNAFSQYKK [SEQ ID NO: 102]
[0209] Collectin neck region of rat SP-D:
SAALRQQMEALNGKLQRLEAAFSRYKK [SEQ ID NO: 1031 [0210] Collectin neck region of bovine conglutinin:
VNALKQRVTILDGHLRRFQNAFSQYKK [SEQ ID NO: 104]
[0211 ] Collectin neck region of bovine collectin:
VDTLRQRMRNLEGEVQRLQNIVTQYRK [SEQ ID NO: 105]
[0212] Neck region of human SP-D:
GSPGLKGDKGIPGDKGAKGESGLPDVASLRQQVEALQGQVQHLQAAFSQYKKVELFPGGIPHRD
[SEQ ID NO: 106]

RECTIFIED SHEET (RULE 91) ISA/EP

[0213] Other examples of a MBP trimerizing domain is described in PCT
Application Serial No.
US08/76266, published as WO 2009/036349, which is incorporated by reference in its entirety.
This trimerizing domain can oligomerize even further and create higher order multimeric complexes.
[0214] The invention also provides for a general and simple procedure for reliable conversion of an initially selected protein derivative into a final protein product, which without further reformatting may be produced in bacteria (e.g. Escherichia coli) both in small and in large scale (International Patent Application Publication No. WO 94/18227 A2). In certain embodiments, several identical or non-identical binding sites can be included in the same functional protein unit by simple and general means, enabling the exploitation even of weak affinities by means of avidity in the interaction, or the construction of bi- or hetero-functional molecular assemblies (International Patent Application Publication No. WO 98/56906, which is incorporated by reference in its entirety). In certain embodiments, binding can be modulated by the addition or removal of divalent metal ions (e.g. calcium ions) in combinational libraries with one or more preserved metal binding site(s) in the CTLDs. Alternatively, binding can be modulated by altering the pH.

[0215) Uses of the CTLD polypeptides [0216] The combinatorial polypeptide libraries of the invention can be used to generate and identify CTLDs with desired binding properties to target molecules of interest for use in a number of applications including, for example, diagnostic or therapeutic applications in which antibody products are typically used as reagents, in biochemical assay systems, medical in vitro or in vivo diagnostic assay systems, or as active components in therapeutic compositions. The combinatorial polypeptide library comprises altered loop regions that allow for the generation of high affinity binding molecules to selected target moieties.

[0217] For use in vitro assay systems, the CTLDs (or CTLD-based protein products) have advantages relative to antibody derivatives as each binding site in a CTLD-based protein product is harbored in a single structurally autonomous protein domain. CTLD domains are resistant to proteolysis, and neither stability nor access to the ligand-binding site is compromised by the attachment of other protein domains to the N- or C-terminus of the CTLD.
Accordingly, the RECTIFIED SHEET (RULE 91) ISA/EP

CTLD binding module may readily be utilized as a building block for the construction of modular molecular assemblies (e.g., N- and/or C-terminal extensions), for example, harboring multiple CTLDs of identical or non-identical specificity, reporter molecules, enzymatic molecules (peroxidases, phosphatases), effector molecules, radioisotopes, or any other signaling molecule known in the art.

[0218) In terms of in vivo use as an essential component of compositions to be used for in vivo diagnostic or therapeutic purposes, the CTLD-based protein products are virtually identical to the corresponding natural CTLD protein already present in the body, and are therefore expected to elicit minimal immunological response in the patient. Single CTLDs are about half the mass of the smallest functional antibody derivative, the single-chain Fv derivative, and this small size may in some applications be advantageous as it may provide better tissue penetration and distribution, as well as a shorter half-life in circulation. Multivalent formats of CTLD proteins, such as those based on the complete tetranectin trimer or the further multimerized collectins, (e.g., mannose binding protein) provide increased binding capacity and avidity and longer circulation half-life.

[0219] It should be noted that the section headings are used herein for organizational purposes only, and are not to be construed as in any way limiting the subject matter described. All references cited herein are incorporated by reference in their entirety for all purposes.

[0220] The Examples that follow are merely illustrative of certain embodiments of the invention, and are not to be taken as limiting the invention, which is defined by the appended claims.

(0221] EXAMPLES

[0222] The vectors discussed in the following Examples (pANA) are derived from vectors that have been previously described [see US 2007/0275393]. Certain vector sequences are provided in the Sequence Listing and one of skill will be able to derive vectors given the description provided herein. The pPhCPAB phage display vector (SEQ ID NO: 50) has the gIII
signal peptide coding region has been fused with a linker to the hTN sequence encoding ALQT (etc.).
The C-terminal end of the CTLD region is fused via a linker to the remaining gIII coding region.
Within the CTLD region, nucleotide mutations were generated that did not alter the coding RECTIFIED SHEET (RULE 91) ISA/EP

sequence but generated restriction sites suitable for cloning PCR fragments containing altered loop regions. A portion of the loop region was removed between these restriction sites so that all library phage could only express recombinants and not wild-type tetranectin.
The murine TN
CTLD phage display vectors are similarly designed. Another embodiment of these vectors is pANA27 (SEQ ID NO: 64) in which the gene III C-terminal region has been truncated and the suppressible stop codon at the end of the hTN coding sequence has been altered to encode glutamine. The murine vector pANA28 (SEQ ID NO: 65) was constructed in a similar fashion.
[0223] Example 1 [0224] Library construction: mutation and extension of Loop 1 [0225] The sequences of human tetranectin and mouse tetranectin, and the positions of loops 1, 2, 3, 4 (LSA) and 5 (LSB) are shown in FIGs. 1, 2 and 4. For the 1-2 extended libraries of human and mouse tetranectin C-type lectin binding domains ("Human 1 X-2" and "Mouse I X-2,"
respectively), the coding sequences for Loop 1 were modified to encode the sequences shown in Table 3, where the five amino acids AAEGT (SEQ ID NO: 579; human) or AAEGA
(SEQ ID
NO: 581; mouse) were substituted with seven random amino acids encoded by the nucleotides NNK NNK NNK NNK NNK NNK NNK (SEQ ID NO: 582); N denotes A, C, G, or T; K
denotes G or T. The amino acid arginine immediately following Loop 2 was also fully randomized by using the nucleotides NNK in the coding strand. This amino acid was randomized because the arginine contacts amino acids in Loop 1, and might constrain the configurations attainable by Loop 1 randomization. In addition, the coding sequence for Loop 4 was altered to encode an alanine (A) instead of Lysine 148 (K) in order to abrogate plasminogen binding, which.has been shown to be dependent on the Loop 4 lysine (Graversen et al., 1998).
The sequences of human tetranectin and mouse tetranectin, and the positions of Loops 1, 2, 3, 4, and 5 are shown in FIG. 2.

Amino acids of loop regions from human and mouse tetranectin (TN).
Parentheses indicate neighboring amino acids not considered part of the loop.
X = any amino acid.

RECTIFIED SHEET (RULE 91) ISA/EP

Loop 1 Loop 2 Loop 3 Loop 4 Loop S Library ISEQ ID NO] [SEQ D [SEQ ID NO] ISEQ ID NO) NOI
Human DMAAEGTW DMTGA(R) NWETEITAQ(P) DGGKTEN AAN
TN [107] [108] [109] [110]
Human DMXXXXXXXW DMTGA(X) NWETEITAQ(P) DGGATEN AAN
1X-2 [111] [112] [109] [113]
Human DMXXXXXW DMXXX(X) NWETEITAQ(P) DGGATEN AAN
1-2 [114] [115] [109] [113]
Human XXXXXXXW DMTGA(R) NWETEITAQ(P) DGGXXXXXEN AAN
1-4 [116] [108) [109] [117]
Human DMAAEGTW DMTGA(R) NWXXXXXXQ(P) DGGATEN AAN
3X 6 [107] [108] [118] [113]

Human DMAAEGTW DMTGA(R) NWXXXXXXXQ(P) DGGATEN AAN
3X 7 [107] [108] (119] [113]

Human DMAAEGTW DMTGA(R) NWXXXXXXXXQ(P) DGGATEN AAN
3X 8 [107] [108] [120] [113) Human DMAAEGTW DMTGA(R) NWETEXXXXXXXTAQ(P) DGGATEN AAN
3X loop [107] [108] [121] [113]

Human DMAAEGTW DMTGA(R) NWETXXXXXXAQ(P) DGGXXXXXXN AAN
3-4X [107] [108] [122] [123]
Human DMAAEGTW DMTGA(R) NWEXXXXXX(X) XGGXXXN
3-4 [107] [108] [124] [125] AAN
combo Human DMAAEGTW DMTGA(R) NWEXXXXXQ(P) DGGATEN xxx 3-5 [107) [108] [126] [113]
Human DMAAEGTW DMTGA(R) NWETEITAQ(P) DGGXXXXXXXN AAN
4 [107] [108] [109] [127) Mouse DMAAEGAW DMTGG(L) NWETEITTQ(P) DGGKAEN AAN
TN [128] [129] [130] [131]
Mouse DMXXXXXXXW DMTGG(X) NWETEITTQ(P) DGGAAEN AAN
1X-2 [111] [132] [130] [133]
Mouse DMXXXXXW DMXXX(X) NWETEITTQ(P) DGGAAEN AAN
1-2 [114] [134] [130] [133]

RECTIFIED SHEET (RULE 91) ISA/EP

Loop 1 Loop 2 Loop 3 Loop 4 Loop Library [SEQ ID NO] ISNO ID [SEQ ID NO] [SEQ ID NO]

Mouse XXXXXXXW DMTGG(L) NWETEITTQ(P) DGGXXXXXEN AAN
1-4 [116] [129] [130] [117]
Mouse DMAAEGAW DMTGG(L) NWXXXXXXQ(P) DGGKAEN AAN
3X [128] [129] [118] [131]
Mouse DMAAEGAW DMTGG(L) NWXXXXXXXQ(P) DGGKAEN AAN
3X [128] [129] [119] [131]
Mouse DMAAEGAW DMTGG(L) NWXXXXXXXXQ(P) DGGKAEN AAN
3X [128] [129] [120] [131]
Mouse DMAAEGAW DMTGG(L) NWETEXXXXXXXTTQ(P) DGGKAEN AAN
3X loop [128] [129] [135] [131]

Mouse DMAAEGAW DMTGG(L) NWETXXXXXXTQ(P) DGGXXXXXXN AAN
3-4X [128] [129] [136] [123]
Mouse DMAAEGAW DMTGG(L) NWEXXXXXX(X) XGGXXXN
3-4 [128] [129] [124] [125] AAN
combo Mouse DMAAEGAW DMTGG(L) NWEXXXXXQ(P) DGGKAEN XXX
3-5 [128] [129] [126] [131]
Mouse DMAAEGAW DMTGG(L) NWETEITTQ(P) DGGXXXXXXXN AAN
4 [128] [129] [130] [127]
[0226] The human Loop I extended library was generated using overlap PCR in the following manner (primer sequences are shown in Table 4). Primers 1Xfor (SEQ ID NO: 137) and 1Xrev (SEQ ID NO: 138) were mixed and extended by PCR, and primers BstXl for (SEQ ID
NO: 139) and PstBssRevC (SEQ ID NO: 140) were mixed and extended by PCR. The resulting fragments were purified from gels, and mixed and extended by PCR in the presence of the outer primers Bglforl2 (SEQ ID NO: 141) and PstRev (SEQ ID NO: 142). The resulting fragment was gel purified and cut with Bgl II and Pst I and cloned into a phage display vector pPhCPAB or pANA27. The phage display vector pPhCPAB was derived from pCANTAB (Pharmacia), and contained a portion of the human tetranectin CTLD fused to the M13 gene III
protein. The CTLD region was modified to include BglII and Pstl restriction enzyme sites flanking Loops 1-4, and the 1-4 region was altered to include stop codons, such that no functional gene III protein RECTIFIED SHEET (RULE 91) ISA/EP

could be produced from the vector without ligation of an in-frame insert.
pANA27 was derived from pPhCPAB by replacing the BamHl to C1aI regions with the BamHl to Clal sequence of SEQ ID NO:64 (pANA27). This replaces the amber suppressible stop codon with a glutamine codon and truncates the amino terminal region of gene III.

[0227] Ligated material was transformed into electrocompetent XL1-Blue E. coli (Stratagene) and four to eight liters of cells were grown overnight and DNA isolated to generate a master library DNA stock for panning. A library size of 1.5 x 108 was obtained, and clones examined showed diversified sequence in the targeted regions.

[0228] The mouse Loop I extended library was generated using overlap PCR in the following manner. Primers MulXfor (SEQ ID NO: 143) and MulXrev (SEQ ID NO: 144) were mixed and extended by PCR, and primers MulXSallfor (SEQ ID NO: 145) and MulXPstRev (SEQ ID
NO: 146) were mixed and extended by PCR. The resulting fragments were purified from gels, mixed and extended by PCR in the presence of the outer primers BstBBssH (SEQ
ID NO: 147) and Mu Pst (SEQ ID NO: 148). The resulting fragment was gel purified and cut with BssH II
and Pst I and ligated into similarly digested phage display vector pANA16 or pANA28. Phage display vector pANA16 (SEQ ID NO: 63) was derived from pPhCPAB by replacing the human tetranectin CTLD with the mouse tetranectin CTLD. The mouse tetranectin CTLD
included BstBI, BssHII, and SaII sites within the Loop 1-4 region and a Pstl site after the Loop 4 region similar to pPhCPAB in order to facilitate cloning. In addition, the region was altered to include stop codons as described above. Phage display vector pANA28 (SEQ ID NO:65)was derived from pANA1 6 (SEQ ID NO:63) by replacing the BamHI to Clal region with the BamHI to ClaI
sequence given in SEQ ID NO:65. Ligated material was transformed into electrocompetent XLI -Blue E. coli (Stratagene) and four to eight liters of cells were grown overnight and DNA
isolated to generate a master library DNA stock for panning. A library size of 2.65 X1010 was obtained, and clones examined showed diversified sequence in the targeted regions.

RECTIFIED SHEET (RULE 91) ISA/EP

Sequences used in the generation of phage displayed C-type lectin domain libraries.
M=A or C; N = A, C, G, or T; K = G or T;S=G orC;W=A or T.

Name Sequence SEQ ID
NO
1Xfor GGCTGGGCCT GAACGACATG NNKNNKNNKN NKNNKNNKNN KTGGGTGGAT 137 ATGACTGGCG CC
GGCGGTGATC TCAGTTTCCC AGTTCTTGTA GGCGATMNNG GCGCCAGTCA
1Xrev TATCCACCCA 138 BstXlfor ACTGGGAAAC TGAGATCACC GCCCAACCTG ATGGCGGCGC AACCGAGAAC 139 TGCGCGGTCC TG
PstBssRev CCCTGCAGCG CTTGTCGAAC CACTTGCCGT TGGCGGCGCC AGACAGGACC 140 C GCGCAGTTCT
Bglforl2 GCCGAGATCT GGCTGGGCCT GAACGACATG 141 PstRev ATCCCTGCAG CGCTTGTCGA ACC 142 MulXfor GCTGTTCGAA TACGCGCGCC ACAGCGTGGG CAACGATGCG AACATCTGGC 143 TGGGCCTCAA CGATATG
MulXrev GCCGCCGGTC ATGTCGACCC NNCATATCGT 144 TGAGGCCCAG CCAG
Mu1XSa1Fo TGGGTCGACA TGACCGGCGG CNNKCTGGCC TACAAGAACT GGGAGACGGA 145 r GATCACGACG CAACCCGACG GCGGCGCTGC CGAGAACTG
Mu1XPstRe CAGCGTTTGT CGAACCACTT GCCGTTGGCT GCGCCAGACA GGGCGGCGCA 146 v GTTCTCGGCA GCGCCGCCGT CGGGTT
BstBBssH GCTGTTCGAA TACGCGCGCC ACAGCGTGG 147 Mu Pst GGGCAACTGA TCTCTGCAGC GTTTGTCGAA CCACTTGCCG T 148 1-2 for GGCTGGGCCT GAACGACATG NNKNNKNNKN NKNNKTGGGT GGATATGNNK 149 NNKNNKNNKA TCGCCTACAA GAACTGGGA
GACAGGACGG CGCAGTTCTC GGTTGCGCCG CCATCAGGTT GGGCGGTGAT
1-2 rev CTCAGTTTTC CAGTTCTTGT AGGCGAT 150 PstRevl2 ATCCCTGCAG CGCTTGTCGA ACCACTTGCC GTTGGCGGCG CCAGACAGGA 151 CGGCGCAGTT CTC
Mul2rev CGTCTCCCAG TTCTTGTAGG CCAGMNNNNN MNNMNNCATG TCGACCCAMN 152 NMNNMNNMNN MNNCATATCG TTGAGGCCCA GCCAG
Mu1234for GCCTACAAGA ACTGGGAGAC GGAGATCACG ACGCAACCCG ACGGCGGCGC 153 TACCGAGAAC TG
BglBssfor GAGATCTGGC TGGGCCTCAA CNNSNNSNNS NNSNNSNNSN NSTGGGTGGA 154 CATGACTGGC
BssBglrev TTGCGCGGTG ATCTCAGTCT CCCAGTTCTT GTAGGCGATA CGCGCGCCAG 155 TCATGTCCAC CCA
BssPstfor GACTGAGATC ACCGCGCAAC CCGATGGCGG CNNSNNSNNS NNSNNSGAGA 156 ACTGCGCGGT CCTG
PstBssRev CCCTGCAGCG CTTGTCGAAC CACTTGCCGT TGGCCGCGCC TGACAGGACC 157 GCGCAGTTCT
Bglfor GCCGAGATCT GGCTGGGCCT CA 158 MuUpsF GCCATGGCCG CCTTACAGAC TGTGTGCCTG AAG 159 MuRanR CGTCTCCCAG TTCTTGTAGG CCAGGAGGCC GCCGGTCATG TCCACCCAMN 160 MNNMNNMNNG TTGAGGCCCA GCCAGAT
-NMNNMNNMNN MuRanF GCCTACAAGA ACTGGGAGAC GGAGATCACG ACGCAACCCG ACGGCGGCNN 161 KNNKNNKNNK NNKGAGAACT GCGCCGCCCT G
MuDnsR CGCACCTGCG GCCGCCACAA TGGCAAACTG GCAGATGT 162 RECTIFIED SHEET (RULE 91) ISA/EP

H Loop 1- ATCTGGCTGG GCCTGAACGA CATGGCCGCC GAGGGCACCT GGGTGGATAT 163 H Loop 3- CCGCCATCGG GTTGGGCMNN MNNMNNMNNM NNMNNAGTTT CCCAGTTCTT 164 4 Ext R GTAGGCGATA CG
H Loop 3- GCCCAACCCG ATGGCGGCNN KNNKNNKNNK NNKNNKAACT GCGCCGTCCT 165 4 Ext-F GTCTGGC
H Loop 5- CCTGCAGCGC TTGTCGAACC ACTTGCCGTT GGCGGCGCCA GACAGGACGG 166 R CGCA
M SacII-F GACATGGCCG CGGAAGGCGC CTGGGTCGAC ATGACCGGCG GCCTGCTGGC 167 CTACAAGAAC
M Loop 3- CCGCCGTCGG GTTGGGTMNN MNNMNNMNNM NNMNNGGTCT CCCAGTTCTT 168 4 Ext-R GTAGGCCAGC A
M Loop 3- ACCCAACCCG ACGGCGGCNN KNNKNNKNNK NNKNNKAACT GCGCCGCCCT 169 4 Ext-F GTCTGGC
M Loop 5- CTGATCTCTG CAGCGCTTGT CGAACCACTT GCCGTTGGCT GCGCCAGACA 170 R GGGCGGCGCA GTT
H Loop 3- GCCAGACAGG ACGGCGCAGT TMNNMNNMNN GCCGCCMNNM NNNNNMNNMN 171 4 Combo R NMNDRJNMNN TTCCCAGTTC TTGTAGGCGA TACG
M Loop 3- GCCAGACAGG GCGGCGCAGT TMNNMNN11NN GCCGCCMNNM NNMNNMNNMN 172 4 Combo R NM*RANNMNN CTCCCAGTTC TTGTAGGCCA GCA
H Loop 3- CCGCCATCGG GTTGGGCGGT GATCTCAGTT TCCCAGTTCT TGTAGGCGAT 173 R ACG
H Loop 4 GCCCAACCCG ATGGCGGCNN KNNKNNKNNK NNKNNKNNKA ACTGCGCCGT 174 Ext-F CCTGTCTGGC
M Loop 3- CCGCCGTCGG GTTGGGTGGT GATCTCGGTC TCCCAGTTCT TGTAGGCCAG 175 R CA
M Loop 4 ACCCAACCCG ACGGCGGCNN KNNKNNKNNK NNKNNKNNKA ACTGCGCCGC 176 Ext-F CCTGTCTGGC
HLoop3F 6 CTGGCGCGCG TATCGCCTAC AAGAACTGGN NKNNKNNKNN KNNKNNKCAA 177 CCCGATGGCG GCGCCACCGA GAAC
HLoop3F 7 CTGGCGCGCG TATCGCCTAC AAGAACTGGN NKNNKNNKNN KNNKNNKNNK 178 CAACCCGATG GCGGCGCCAC CGAGAAC
HLoop3F 8 CTGGCGCGCG TATCGCCTAC AAGAACTGGN NKNNKNNKNN KNNKNNKNNK 179 CAACCCGATG GCGGCGCCAC CGAGAAC
HLoop4R CCTGCAGCGC TTGTCGAACC ACTTGCCGTT GGCGGCGCCA GACAGGACGG 180 CGCAGTTCTC GGTGGCGCCG CCATCGGGTT G
HLoop3F 6 GTTCTCGGCA GCGCCGCCGT CGGGTTGMNN NNMNNCCAGT 181 TCTTGTAGGC CAGCAGGCCG CCGGTCA
MLoop3F 7 GTTCTCGGCA GCGCCGCCGT CGGGTTGMNN MNNMNNMNNM NNMNNMNNCC 182 AGTTCTTGTA GGCCAGCAGG CCGCCGGTCA
GTTCTCGGCA GCGCCGCCGT CGGGTTGMNN
HLoop3F 8 NCCAGTTCTT GTAGGCCAGC AGGCCGCCGG TCA 183 MNMNMNM NNNNNCTCCC AGTTCTTGTA GGCGATACG
PstLoop4 ATCCCTGCAG CGCTTGTCGA ACCACTTGCC GTTGGCCGCG CCTGACAGGA 186 rev CCGCGCAGTT CTCGCC
Loop3AF2 GAGCGTGGGCAACGAGGCCGAGATCTGGCTGGGCCTCAACGACATGGCCGCCGA 187 Loop3AR2 CCAGTTCTTGTAGGCGATACGCGCGCCAGTCATATCCACCCAGGTGCCCTCGGC 188 GGCCATGTCGTTGAGG
Loop3BF ATCGCCTACAAGAACTGGGAGACTGRGNNKNNKNNKNNKNNKNNKNNKACCGCG 189 CAACCCGATGGCGGTGCAAC
Loop3BR CGCTTGTCGAACCACTTGCCGTTGGCGGCGCCAGACAGGACGGCGCAGTTCTCG 190 GTTGCACCGCCATCGGGTTG
Loop30R GATCCCTGCAGCGCTTGTCGAACCACTTGCCGT 191 RECTIFIED SHEET (RULE 91) ISA/EP

HuBglfor GCCGAGATCTGGCTGGGCCTGA 193 ATGACTGGC

BssBglrev GTCCACCCA
FGVFGfor GACTGAGATCACCGCGCAACCCGATGGCGGCTTCGGCGTGTTCGGCGAGAACTG 196 CGCGGTCCTG
WGVFGfor GACTGAGATCACCGCGCAACCCGATGGCGGCTGGGGCGTGTTCGGCGAGAACTG 197 CGCGGTCCTG
FGYFGfor GACTGAGATCACCGCGCAACCCGATGGCGGCTTCGGGTACTTCGGCGAGAACTG 198 CGCGGTCCTG
WGYFGfor GACTGAGATCACCGCGCAACCCGATGGCGGCTGGGGGTACTTCGGCGAGAACTG 199 CGCGGTCCTG
WGVWGfor GACTGAGATCACCGCGCAACCCGATGGCGGCTGGGGCGTGTGGGGCGAGAACTG 200 CGCGGTCCTG

Mu 1-4 AF TGGGTCGACATGACCGGC

Mu 1-4 AR ATGTCGACCCA

Mu 1-4 BF TGCTGCCCTGTCTGG

Mu 1-4 BR AGTTCTC
Mu 1-4 OF ATACGCGCGCCACAGCGTGGGCAACGATGCGAACATCTG 205 Mu 1-4 OR ATCTCTGCAGCGCTTGTCGAACC 206 Mloop4F GGCAAGTG

M MfeR TGCGCCAGAC

m3-5 for AGCTGAGAACTG

m3-5 rev AGCTGCGCCGCCGT
m3-5 OF CTGGGTCGACATGACCGGCGGCCTGCTGGCCTACAAGAACTGGGAG 211 m3-5 OR ATCTCTGCAGCGCTTGTCGAACCACTTG 212 h3-5AF TGGGCCTGAACGACATGGCCGCCGAGGGCACCTGGGTGGATATGACTGGCGCGC 213 GTATCGCCTACAAGAACTGGGAG
h3-5AR GTTGCGCCGCCATCGGGTTG CTCCCAGTTCTTGTAGGCG 214 ATACG
h3-SBF CAACCCGATGGCGGCGCAACCGAGAACTGCGCCGTCCTGTCTGG 215 h3-5BR TGTAGGGCAATTGATCCCTGCAGCGCTTGTCGAACCACTTGCCMNNMNNMNNGC 216 CAGACAGGACGGCGCAGTT
h3-5 OF GCCGAGATCTGGCTGGGCCTGAACGACATGG 217 Example 2 [0229] Library construction: mutation of Loops I and 2 [0230] For the Loop 1-2 libraries of human and mouse tetranectin C-type lectin binding domains ("Human 1-2" and "Mouse 1-2," respectively), the coding sequences for Loop I
were modified RECTIFIED SHEET (RULE 91) ISA/EP

to encode the sequences shown in Table 1, where the five amino acids AAEGT
(SEQ ID NO:
579; human) or AAEGA (SEQ ID NO: 581; mouse) were replaced with five random amino acids encoded by the nucleotides NNK NNK NNK NNK NNK (SEQ ID NO: 583); N denotes A, C, G, or T; K denotes G or T). In Loop 2 (including the neighboring arginine), the four amino acids TGAR (SEQ ID NO: 584) in human or TGGR (SEQ ID NO: 585) in mouse were replaced with four random amino acids encoded by the nucleotides NNK NNK NNK NNK (SEQ ID NO:
586).
In addition, the coding sequence for Loop 4 was altered to encode an alanine (A) instead of the lysine (K) in the loop, in order to abrogate plasminogen binding, which has been shown to be dependent on the Loop 4 lysine (Graversen et al., 1998).

[0231 ] The human 1-2 library was generated using overlap PCR in the following manner (primer sequences are shown in Table 4). Primers 1-2 for (SEQ ID NO: 149) and 1-2 rev (SEQ ID NO:
150) were mixed and extended by PCR. The resulting fragment was purified from gels, mixed and extended by PCR in the presence of the outer primers Bglforl 2 (SEQ ID NO:
141) and PstRevl2 (SEQ ID NO: 151). The resulting fragment was gel purified and cut with Bgl II and Pst I and cloned into similarly digested phage display vector pPhCPAB or pANA27, as described above. A library size of 4.86 x 108 was obtained, and clones examined showed diversified sequence in the targeted regions.

[0232] The mouse Loop 1-2 library was generated using overlap PCR in the following manner.
Primers MulXfor (SEQ ID NO: 143) and Mul2rev (SEQ ID NO: 152) were mixed and extended by PCR, and primers Mu 1234for (SEQ ID NO: 153) and Mu 1 XPstRev (SEQ ID NO:
146) were mixed and extended by PCR. The resulting fragments were purified from gels, mixed and extended by PCR in the presence of the outer primers BstBBssH (SEQ ID NO: 147) and Mu Pst (SEQ ID NO: 148). The resulting fragment was gel purified and cut with BssH II
and Pst I and cloned into similarly digested phage display vector pANA16 or pANA28, as described above. A
library size of 1.63.x 109 was obtained, and clones examined showed diversified sequence in the targeted regions.

Example 3 [0233] Library construction: mutation and extension of Loops 1 and 4 RECTIFIED SHEET (RULE 91) ISA/EP

[0234] For the Loop 1-4 libraries of human and mouse tetranectin C-type lectin binding domains ("Human 1-4" and "Mouse 1-4," respectively), the coding sequences for Loop I
were modified to encode the sequences shown in Table 3, where the seven amino acids DMAAEGT
(see SEQ
ID NO: 587; human) or DMAAEGA (see SEQ ID NO: 588; mouse) were replaced with seven random amino acids encoded by the nucleotides NNK NNK NNK NNK NNK NNK NNK (SEQ
ID NO: 582); N denotes A, C, G, or T; K denotes G or T). In Loop 4 two amino acids KT in human or KA in mouse, were replaced with five random amino acids encoded by the nucleotides NNK NNK NNK NNK NNK (SEQ ID NO: 583).

[0235] The human 1-4 library was generated using overlap PCR in the following manner (primer sequences are shown in Table 4). Primers BglBssfor (SEQ ID NO: 154) and BssBglrev (SEQ ID
NO: 155) were mixed and extended by PCR, and primers BssPstfor (SEQ ID NO:
156) and PstBssRev (SEQ ID NO: 157) were mixed and extended by PCR. The resulting fragments were purified from gels, mixed and extended by PCR in the presence of the outer primers Bglfor (SEQ
ID NO: 158) and PstRev (SEQ ID NO: 142). The resulting fragment was gel purified and cut with Bg1 II and Pst I restriction enzymes, and cloned into similarly digested phage display vector pPhCPAB or pANA27, as described above. A library size of 2 x 109 was obtained, and 12 clones examined prior to panning showed diversified sequence in the targeted regions.

[0236] The mouse 1-4 library was generated using overlap PCR in the following manner (primer sequences are shown in Table 4). Primers Mu 1-4 AF (SEQ ID NO: 201) and Mu 1-4 AR (SEQ
ID NO: 202) were mixed and extended by PCR, and primers Mu 1-4 BF (SEQ ID NO:
203) and Mu 1-4 BR (SEQ ID NO: 204) were mixed and extended by PCR. The resulting fragments were purified from gels, mixed and extended by PCR in the presence of the outer primers Mu 1-4 OF
(SEQ ID NO: 205) and Mu 1-4 OR (SEQ ID NO: 206). The resulting fragment was gel purified and cut with BstB I and Pst I restriction enzymes, and cloned into similarly digested phage display vector pANA28, as described above. A library size of 4.7 x 109 was obtained, and >20 clones were examined prior to panning showed diversified sequence in the targeted regions.
Example 4 [0237] Library construction: mutation and extension of Loops 3 and 4 RECTIFIED SHEET (RULE 91) ISA/EP

[0238] For the Loop 3-4 extended libraries of human and mouse tetranectin C-type lectin binding domains ("Human 3-4X" and "Mouse 3-4X," respectively), the coding sequences for Loop 3 were modified to encode the sequences shown in Table 4, where the three amino acids EIT of human or mouse tetranectin were replaced with six random amino acids encoded by the nucleotides NNK NNK NNK NNK NNK NNK (SEQ ID NO: 589) in the coding strand (N
denotes A, C, G, or T; K denotes G or T). In addition, in Loop 4, the three amino acids KTE in human or KAE in mouse were replaced with six random amino acids encoded by the nucleotides NNK NNK NNK NNK NNK NNK (SEQ ID NO: 589).

[0239] The human 3-4 extended library was generated using overlap PCR in the following manner (primer sequences are shown in Table 4). Primers H Loop 1-2-F (SEQ ID
NO: 163) and H Loop 3-4 Ext-R (SEQ ID NO: 164) were mixed and extended by PCR, and primers H Loop 3-4 Ext-F (SEQ ID NO: 165) and H Loop 5-R (SEQ ID NO: 166) were mixed and extended by PCR. The resulting fragments were purified from gels, and mixed and extended by PCR in the presence of additional H Loop 1-2-F (SEQ ID NO: 163) and H Loop 5-R (SEQ ID
NO: 166).
The resulting fragment was gel purified and cut with Bgl II and Pst I
restriction enzymes, and cloned into similarly digested phage display vector pPhCPAB or pANA27, as described above.
A library size of 7.9 x 108 was obtained, and clones examined showed diversified sequence in the targeted regions.

[0240] The mouse 3-4 extended library was generated using overlap PCR in the following manner. Primers M SacII-F (SEQ ID NO: 167) and M Loop 3-4 Ext-R (SEQ ID NO:
168) were mixed and extended by PCR, and primers M Loop 3-4 Ext-F (SEQ ID NO: 169) and M
Loop 5-R (SEQ ID NO: 170) were mixed and extended by PCR. The resulting fragments were purified from gels, and mixed and extended by PCR in the presence of additional M SacII-F (SEQ ID
NO: 167) and M Loop 5-R (SEQ ID NO: 170). The resulting fragment was gel purified and cut with Sac II and Pst I restriction enzymes, and cloned into similarly digested phage display vector pANA16 or pANA28, as described above. A library size of 4.95 x 109 was obtained, and clones examined showed diversified sequence in the targeted regions.

Example 5 RECTIFIED SHEET (RULE 91) ISA/EP

[0241 ] Library construction: mutation of Loops 3 and 4 and the PRO between the loops [0242] For the Loop 3-4 combo library of human and mouse tetranectin C-type lectin binding domains ("Human 3-4 combo" and "Mouse 3-4 combo," respectively), the coding sequences for loops 3 and 4 and the proline between these two loops were altered to encode the sequences shown in Table 3, where the human sequence TEITAQPDGGKTE (SEQ ID NO: 590) or the corresponding mouse sequence TEITTQPDGGKAE (SEQ ID NO: 591) were replaced by the 13 amino acid sequence XXXXXXXXGGXXX, (SEQ ID NO: 592) where X represents a random amino acid encoded by the sequence NNK (N denotes A, C, G, or T; K denotes G
or T).

[0243] The human 3-4 combo library was generated using overlap PCR in the following manner (primer sequences are shown in Table 4). Primers H Loop 1-2-F (SEQ ID NO: 163) and H Loop 3-4 Combo-R (SEQ ID NO: 171) were mixed and extended by PCR and the resulting fragment was purified from gels and mixed and extended by PCR in the presence of additional H Loop 1-2-F (SEQ ID NO: 163) and H loop 5-R (SEQ ID NO: 166). The resulting fragment was gel purified and cut with Bgl 11 and Pst I restriction enzymes, and cloned into similarly digested phage display vector pPhCPAB or pANA27, as described above. A library size of 4.95 x 109 was obtained, and clones examined showed diversified sequence in the targeted regions.

[0244] The mouse 3-4 combo library was generated using overlap PCR in the following manner.
Primers M SacII-F (SEQ ID NO: 167) and M Loop 3-4 Combo-R (SEQ ID NO: 172) were mixed and extended by PCR and the resulting fragment was purified from gels and mixed and extended by PCR in the presence of the outer primers M SacII-F (SEQ ID NO:
167) and M Loop 5-R (SEQ ID NO: 170). The resulting fragment was gel purified and cut with Sac II and Pst I
restriction enzymes, and cloned into similarly digested phage display vector pANA16 or pANA28, as described above. A library size of 7.29 x 108 was obtained, and clones examined showed diversified sequence in the targeted regions.

Example 6 [0245] Library construction: mutation and extension of Loop 4 [0246] For the Loop 4 extended libraries of human and mouse tetranectin C-type lectin binding RECTIFIED SHEET (RULE 91) ISA/EP

domains ("Human 4" and "Mouse 4," respectively), the coding sequences for Loop 4 were modified to encode the sequences shown in Table 3, where the three amino acids KTE of human or KAE of mouse tetranectin were replaced with seven random amino acids encoded by the nucleotides NNK NNK NNK NNK NNK NNK NNK (SEQ ID NO: 582); N denotes A, C, G, or T; K denotes G or T).

[0247] The human 4 extended library was generated using overlap PCR in the following manner (primer sequences are shown in Table 4). Primers H Loop 1-2-F (SEQ ID NO: 163) and H Loop 3-R (SEQ ID NO: 173) were mixed and extended by PCR, and primers H Loop 4 Ext-F (SEQ ID
NO: 174) and H Loop 5-R (SEQ ID NO: 166) were mixed and extended by PCR. The resulting fragments were purified from gels, and mixed and extended by PCR in the presence of additional H Loop 1-2-F (SEQ ID NO: 163) and H Loop 5-R (SEQ ID NO: 166). The resulting fragment gel purified and was cut with Bgl 11 and Pst I restriction enzymes, and cloned into similarly digested phage display vector pPhCPAB or pANA27, as described above. A library size of 2.7 x 109 was obtained, and clones examined showed diversified sequence in the targeted regions.
[0248] The mouse 4 extended library was generated using overlap PCR in the following manner.
Primers M SacII-F (SEQ ID NO: 167) and M Loop 3-R (SEQ ID NO: 175) were mixed and extended by PCR, and primers M Loop 4 Ext-F (SEQ ID NO: 176) and M Loop 5-R
(SEQ ID
NO: 170) were mixed and extended by PCR. The resulting fragments were purified from gels, and mixed and extended by PCR in the presence of the additional M SacII-F (SEQ
ID NO: 167) and M Loop 5-R (SEQ ID NO: 170). The resulting fragment was gel purified, digested with SacII and PstI restriction enzymes, and cloned into similarly digested phage display vector pANA16 or pANA28, as described above.

Example 7 [0249] Library construction: mutation with and without extension of Loop 3 [0250] For the Loop 3 altered libraries of human and mouse tetranectin C-type lectin binding domains, the coding sequences for Loop 3 were modified to encode the sequences shown in Table 3, where the six amino acids ETEITA (SEQ ID NO: 593) of human or ETEITT
(SEQ ID
NO: 594) of mouse tetranectin were replaced with six, seven, or eight random amino acids RECTIFIED SHEET (RULE 91) ISA/EP

encoded by the nucleotides NNK NNK NNK NNK NNK NNK (SEQ ID NO: 583), NNK NNK
NNK NNK NNK NNK NNK (SEQ ID NO: 582), and NNK NNK NNK NNK NNK NNK NNK
NNK (SEQ ID NO: 595); N denotes A, C, G, or T; and K denotes G or T. In addition, in Loop 4, the three amino acids KTE in human or KAE in mouse were replaced with six random amino acids encoded by the nucleotides NNK NNK NNK NNK NNK NNK (SEQ ID NO: 589). In addition the coding sequence for loop 4 was altered to encode an alanine (A) instead of the lysine (K) in the loop, in order to abrogate plasminogen binding, which has been shown to be dependent on the loop 4 lysine (Graversen et al., 1998).

[0251 ] The human Loop 3 altered library was generated using overlap PCR in the following manner. Primers HLoop3F6, HLoop3F7, and HLoop3F8 (SEQ ID NOS: 177-179, respectively) were individually mixed with HLoop4R (SEQ ID NO: 180) and extended by PCR. The resulting fragments were purified from gels, and mixed and extended by PCR in the presence of oligos H
Loop 1-2F (SEQ ID NO: 163), HuBglfor (SEQ ID NO: 193) and PstRev (SEQ ID NO:
142). The resulting fragments were gel purified, digested with BgII and Pstl restriction enzymes, and cloned into similarly digested phage display vector pPhCPAB or pANA27, as above. After library generation, the three libraries were pooled for panning.

[0252] The mouse Loop 3 altered library was generated using overlap PCR in the following manner. Primers MLoop3F 6, MLoop3F 7, and MLoop3F 8 (SEQ ID NOS: 181-183, respectively) were individually mixed with primer M Sacll-F (SEQ ID NO: 167) and extended by PCR. In addition, primers MLoop4F (SEQ ID NO: 207) and M MfeR (SEQ ID NO:
208) were mixed and extended by PCR. The resulting fragments were purified from gels, mixed, and subjected to PCR in the presence of primers M 3X OF (SEQ ID NO: 184) and M 3X
OR (SEQ
ID NO: 192). Products were digested with Sal I (or Sac II) and Pstl restriction enzymes, and the purified fragments were cloned into similarly digested phage display vector pANA16 or pANA28, as described above.

[0253] Alternate loop extension of loop 3 [0254] The human loop 3 loop library was generated using overlap PCR in the following manner. Primers Loop3AF2 (SEQ ID NO: 187) and Loop3AR2 (SEQ ID NO: 188) are mixed and extended by PCR, and primers Loop3BF (SEQ ID NO: 189) and Loop3BR (SEQ ID
NO:

RECTIFIED SHEET (RULE 91) ISA/EP

190) are mixed and extended by PCR. The resulting fragments are purified from gels, mixed, and subjected to PCR in the presence of primers Bgl for (SEQ ID NO: 158) and Loop3OR (SEQ ID
NO: 191). Products are digested with Bgl II and Pst I restriction enzymes, and the purified fragments are cloned into similarly digested phage display vector pPhCPAB or pANA27, as above. In addition the coding sequence for loop 4 was altered to encode an alanine (A) instead of the lysine (K) in the loop, in order to abrogate plasminogen binding, which has been shown to be dependent on the loop 4 lysine (Graversen et al., 1998). A similar approach can be used to generate the corresponding mouse TN library.

[0255] Example 8 [0256] Mutation of loops 3 and 5 [0257] For the loop 3 and 5 altered libraries of human and mouse tetranectin C-type lectin binding domains, the coding sequences for loops 3 and 5 were modified to encode the sequences shown in Table 3, where the five amino acids TEITA (SEQ ID NO: 596) of human or TEITT
(SEQ ID NO: 597) of mouse tetranectin were replaced with five amino acids encoded by the nucleotides NNK NNK NNK NNK NNK (SEQ ID NO: 583), and the three Loop 5 amino acids AAN of human or mouse were replaced with three amino acids encoded by the nucleotides NNK
NNK NNK. In addition the coding sequence for loop 4 was altered to encode an alanine (A) instead of the lysine (K) in the loop, in order to abrogate plasminogen binding, which has been shown to be dependent o n the loop 4 lysine (Graversen et at., 1998).

[0258] The human loop 3 and 5 altered library was generated using overlap PCR
in the following manner. Primers h3-5AF (SEQ ID NO: 213) and h3-5AR (SEQ ID NO: 214) were mixed and extended by PCR, and primers h3-5BF (SEQ ID NO: 215) and h3-5 BR
(SEQ ID NO:
216) were mixed and extended by PCR. The resulting fragments were purified from gels, and mixed and extended by PCR in the presence of h3-5 OF (SEQ ID NO: 217) and PstRev (SEQ ID
NO: 142). The resulting fragment was gel purified, digested with Bgl I and Pst I restriction enzymes, and cloned into similarly digested phage display vector pPhCPAB or pANA27 as described above.

[0259] The mouse loop 3 and 5 altered library was generated using overlap PCR
in the following RECTIFIED SHEET (RULE 91) ISA/EP

manner. Primers m3-5 for (SEQ ID NO: 209) and m3-5 rev (SEQ ID NO: 210) were mixed and extended by PCR. The resulting fragment was purified from gels, and reamplified by PCR with primers m3-5 OF (SEQ ID NO: 211) and m3-5 OR (SEQ ID NO: 212). Products were digested with Sal I and Pst I restriction enzymes, and the purified fragments were cloned into similarly digested phage display vector pANA16 or pANA28 as described above.

[0260) Examples 9-22 provide exemplary methods for isolating polypeptide sequences specific for TRAIL death receptors using the combinatorial polypeptide libraries of the invention. TRAIL
(tumor necrosis factor-related apoptosis-inducing ligand, also referred to in the literature as Apo2L and TNFSFl0, among other things) belongs to the tumor necrosis factor (TNF) superfamily and has been identified as an activator of programmed cell death, or apoptosis, in tumor cells. TRAIL is expressed in cells of the immune system including NK
cells, T cells, macrophages, and dendritic cells and is located in the cell membrane. TRAIL
can be processed by cysteine proteases, generating a soluble form of the protein. Both the membrane-bound and soluble forms of TRAIL function as trimers and are able to trigger apoptosis via interaction with TRAIL receptors located on target cells. In humans, five receptors have been identified to have binding activity for TRAIL. Two of these five receptors, TRAIL-RI (DR4, TNFSFI
Oa) and TRAIL-R2 (DRS, TNFRSFIOb), contain a cytoplasmic region called the death domain (DD).
The death domain on these two receptor molecules is required for TRAIL-activation of the extrinsic apoptotic pathway upon the binding of TRAIL to the receptors. The remaining three TRAIL receptors (called TRAIL-R3 (DcRI, TNFRSF10c), TRAIL-R4 (DcR2, TNFRSF10d) and circulating osteoprotegerin (OPG, TNFRSFI lb)) are thought to serve as decoy receptors. These three receptors lack functional DDs and are thought to be mainly involved in negatively regulating apoptosis by sequestering TRAIL or stimulating pro-survival signals.

[0261] Upon binding of TRAIL to TRAIL-RI (DR4) or -R2 (DR5) the trimerized receptors recruit several cytosolic proteins that form the death-inducing signaling complex (DISC) which subsequently leads to activation of caspase-8 or caspase-10. This triggers one of two different routes that cause irreversible cell death, one in which caspase-8 directly activates the effector caspases (caspases-3, -6, -7) leading to the disassembly of the cell, and the other route involving the caspase-8 dependent cleavage of the pro-death Bcl-2 family protein, Bid, and engaging the mitochondrial or intrinsic death pathway.

RECTIFIED SHEET (RULE 91) ISA/EP

[0262] In light of this cell death activity, molecules that bind to TRAIL-RI
and TRAIL-R2 may have a therapeutic role in the treatment of a wide variety of cancers.
Accordingly, the CTLD
polypeptide libraries of the invention were screen in an effort to identify and isolate CTLD-based polypeptides having specific binding activity to TRAILRI and TRAIL R2.

[0263] Example 9 [0264] Panning & Screening of human library 1-4 [0265] Phage generated from human library 1-4 were panned on recombinant TRAIL
RI
(DR4)/Fc chimera, and TRAIL R2 (DR5)/Fc chimera. Screening of these binding panels after three, four, and/or five rounds of panning using an ELISA plate assay identified receptor-specific binders in all cases.

[0266] Example 10 [0267] Construction of libraries and clones for selection and screening of agonists for TRAIL
receptors DR4 and DR5 [0268] Phage libraries expressing linear or cyclized randomized peptides of varying lengths can be purchased commercially from manufacturers such as New England Biolabs (NEB).
Alternatively, phage display libraries containing randomized peptides in loops of the C-type lectin domain (CTLD) of human tetranectin can be generated. Loops 1, 2, 3, and 4 of the LSA of CTLD are shown in Fig. 4. Amino acids within these loops can be randomized using an NNS or NNK overlapping PCR mutagenesis strategy. From one to seven codons in any one loop may be replaced by a mutagenic NNS or NNK codon to generate libraries for screening;
alternatively, the number of mutagenized amino acids may exceed the number being replaced (two amino acids may be replaced by five, for example, to make larger randomized loops).
In addition, more than one loop may be altered at the same time. The overlap PCR strategy can generate either a Kpn I site in the final DNA construct between loops 2 and 3, which alters one of the amino acids between the loops, exchanging a threonine for the original alanine.
Alternatively, a BssH II site can be incorporated between loops 2 and 3 that does not alter the original amino acid sequence.
[0269] Example 11 RECTIFIED SHEET (RULE 91) ISA/EP

[0270] Selection and screening of agonists for TRAIL receptors DR4 and DR5 [0271 ] Bacterial colonies expressing phage were generated by infection or transfection of bacteria such as E. coli TG-1 or XL-1 Blue using either glycerol phage stocks of phage libraries or library DNA, respectively. Fifty milliliters of infected/transfected bacteria at an 0.13-600 Of 1 -0 are grown for 15 min at room temperature (RT), after which time 40% of the final concentration of selectable drug marker is added to the culture and incubated for I h at 37 C. Following that incubation the remaining drug for selection is added and incubated for another hour at 37 C.
Helper phage VCS M13 are added and incubated for 2 h. Kanamycin (70 g/mL) is added to the culture, which is then incubated overnight at 37 C with shaking. Phage are harvested by centrifugation followed by cold precipitation of phage from supernatant with one third volume of 20% polyethylene glycol (PEG) 8000/2.5 M NaCl. Phage are resuspended in a buffer containing a protease inhibitor cocktail (Roche Complete Mini EDTA-free) and are subsequently sterile filtered. Phage libraries are titered in E. coli TG-1, XLI -Blue, or other appropriate bacterial host.
[0272] Phage are panned in rounds of positive selection against human DR4 and/or DR5. Human DR4 and DR5 (aka human TRAIL death receptors I and 2) are commercially available in a soluble form (Antigenix America, Cell Sciences, or as Fc (Genway Biotech, R&D
Systems) or GST fusions (Novus Biologicals). Soluble DR4 or DR5 in PBS is bound directly to a solid support, such as the bottom of a microplate well (Immulon 2B ,plates) or to magnetic beads such as Dynabeads. About 250 ng to 500 ng of soluble DR4 or DR5 is bound to the solid substrate by incubation overnight in PBS at either 4 C or RT. The plates (or beads) are then washed three times in PBS/0.05% Tween 20, followed by addition of a blocking agent such as I% BSA, 0.05% sodium azide in PBS and is incubated for at least 0.5 h at RT to prevent binding of material in future steps to non-specific surfaces. Blocking agents such as PBS
with 3% non-fat dry milk or boiled casein can also be used.

[0273] In an alternative protocol, in order to bind DR4 or DR5 Fc fusion proteins, plates or beads are first incubated with 0.5-1 g of a commercially available anti-Fe antibody in PBS. The plates (or beads) are washed and blocked with 1% BSA, 0.05% sodium azide in PBS as above, and are then incubated with death receptor fusion protein at 5 g/mL and incubated for 2 h at RT. Plates are then washed three times with PBS/0.05% Tween 20.

RECTIFIED SHEET (RULE 91) ISA/EP

[0274] Phage libraries at a concentration of about 1011 or 1012 pfu/mL are added to the wells (or beads) containing directly or indirectly bound death receptor. Phage are incubated for at least 2 h at RT, although to screen for different binding properties the incubation time and temperature can be varied. Wells are washed at least eight times with PBS/0.05% Tween 20, followed by PBS washes (8x). Wells can be washed in later rounds of selection with increasingly acidic buffers, such as 100 mM Tris pH 5.0, Tris pH 4.0, and Tris pH 3Ø Bound phages are eluted by trypsin digestion (100 L of I mg/mL trypsin in PBS for 30 min). Bound phages can also be eluted using 0.1 M glycine, pH 2.2. Alternatively, bound phages can be eluted using TRAIL
(available commercially from AbD Serotec) to select for CTLDs or peptides that compete with TRAIL for binding to the death receptors. Further, bound phage can be eluted with compounds that are known to compete with TRAIL for death receptor binding.

[0275] Eluted phage are incubated for 15 min with 10 mL of freshly grown bacteria at an OD600 of 0.8, and the infected bacteria are treated as above to generate phage for the second round of panning. Two or three additional rounds of positive panning are performed.

[0276] As an alternative to using DR4 and/or DR5 directly or indirectly bound to a support, DR4 and/or DR5 expressed endogenously by cancer cell lines or expressed by transfected cells such as 293 cells may be used in rounds of positive selection. For transfected cells, transfection is performed two days prior to panning using the Qiagen AttracteneTM protocol, for example, and an appropriate expression plasmid such as pcDNA3. 1, pCEP4, or pCEP5 bearing DR4 or DR5.
Cells are dissociated in a non-trypsin dissociation buffer and 6 x 106 cells are resuspended in 2 mL IMDM buffer. Phage to be panned are dialyzed prior to being added to cells and incubated for 2 h, RT. Cells are washed by pelleting and resuspending multiple times in IMDM, and phage are eluted with glycine buffer.

[0277] In order to select those peptides that have affinity for DR4 and/or DR5 but not decoy receptors, negative selection rounds or negative selection concomitant with positive selection are performed. Negative selection is done using the decoy receptors DcR1, DcR2, soluble DcR3, and/or osteoprotegerin (OPG, R&D systems). OPG and soluble DcR3 are commercially available(GeneTex, R&D systems), as are DcRI and DcR2 conjugated to Fcor GST
(R&D
Systems, Novus Biologicals). For negative selection rounds, decoy receptor is bound to plates or RECTIFIED SHEET (RULE 91) ISA/EP

beads and blocked as described above for positive rounds of selection. Beads are more desirable as a larger surface area of negative selection molecules can be exposed to the library being panned. The primary library or the phage from other rounds of positive selection are incubated with the decoy receptors for 2 h at room temperature, or overnight at 4 C.
Unbound phage are then removed and subjected to a positive round of selection.

[0278] Positive selection is also performed simultaneously with negative selection. Wells or beads coated with soluble DR4 or DR5 are blocked and exposed to the primary library or phage from a selection round as described above, but a decoy receptor such as DcR1 is included at a concentration of 10 pg/mL. Incubation time may be extended from 2 h to several days at 4 C
prior to elution in this strategy in order to obtain phage with greater specificity and affinity for DR4 or DR5. Negative selection using DR4, in order to obtain DR5-specific, or DR5, in order to obtain DR4-specific binders, can also be performed using the approaches detailed above.

[0279] Negative selection can also be performed on cancerous or transfected cells that express one or more of the decoy receptors. Negative selection is performed similarly to positive selection as described above except that phage are recovered from the supernatant after spinning cells down after incubation and then used in a positive round of selection.

[0280] Example 12 [0281] Plasmid construction of trimeric TRAIL receptor agonists and trimeric CTLD-derived TRAIL receptor agonists [0282] The various versions of trimeric TRAIL receptor agonists and trimeric CTLD-derived TRAIL receptor agonists from phage display or from peptide-grafted, peptide-trimerization domain (TD) fusions, peptide-TD-CTLD fusion, or their various combinations are sub-cloned into bacterial expression vectors (pT7 in house vector, or pET, NovaGen) and mammalian expression vectors (pCEP4, pcDNA3, Invitrogen) for small scale or large-scale production.
[0283] Primers are designed to PCR amplify DNA fragments of binders/agonists from various functional display vectors from Example 1. Primers for the 5'-end are flanked with BamH I
restriction sites and are in frame with the leader sequence in the vector pT7CIIH6. 5' primers also can be incorporated with a cleavage site for protease Granzyme B or Factor Xa. 3' primers RECTIFIED SHEET (RULE 91) ISA/EP

are flanked with EcoRI restriction sites. PCR products are digested with BamHUEcoRI, and then ligated into pT7CIIH6 digested with the same enzymes, to create bacterial expression vectors pT7CIIH6-TRAILa.

[0284] The TRAIL receptor agonist DNAs can be sub-cloned into vector pT7CIIH6 or pET28a (NovoGen), without any leader sequences and 6XHis. 5' primers are flanked with Ndel restriction sites and 3' primers are flanked with EcoRI restriction sites. PCR
products are digested with NdeI/EcoRI, and ligated into the vectors digested with the same enzymes, to create expression vectors pT7-TRAILa and pET-TRAILa.

[0285] The TRAIL receptor agonist DNAs can be sub-cloned into vector pT7CIIH6 or pET28a (NovoGen), with a secretion signal peptide. Expressed proteins are exported into bacterial periplasm, and secretion signal peptide is removed during translocation. 5' primers are flanked with NdeI restriction sites and the primers are incorporated into a bacterial secretion signal peptide, Pe1B, OmpA or OmpT. 3' primers are flanked with EcoRlrestriction sites. A 6xHis tag coding sequence can optionally be incorporated into the 3' primers. PCR
products are digested with NdeI/EcoRI, and ligated into vectors that are digested with the same enzymes, to create the expression vectors pT7-sTRAILa, pET-sTRAILa, pT7-sTRAILaHis, and pET-sTRAILHis.
[0286] The TRAIL receptor agonist DNAs can also be sub-cloned into mammalian expression vector pCEP4 or pcDNA3. 1, along with a secretion signal peptide. Expressed proteins are secreted into the culture medium, and the secretion signal peptide is removed during the secretion processes. 5' primers are flanked with Nhel restriction sites and the primers are incorporated into a tetranectin secretion signal peptide, or another secretion signal peptide (e.g., Ig peptide). 3' primers are flanked with Xhol restriction sites. A 6xHis tag is optionally incorporated into the 3' primers. PCR products are digested with NheUXhoI, and ligated into the vectors that are digested with the same enzymes, to create expression vectors pCEP4-TRAILa, pcDNA-TRAILa, pCEP4-TRAILaHis, and pcDNA-TRAILaHis.

[0287] Example 13 [0288] Expression and purification of TRAIL receptor agonists from bacteria [0289] Bacterial expression constructs are transformed into bacterial strain BL2I (DE3) RECTIFIED SHEET (RULE 91) ISA/EP

(Invitrogen). A single colony on a fresh plate is inoculated into 100 mL of 2xYT medium in a shaker flask. The flask is incubated in a shaker rotating at 250 rpm at 37 C
for 12 h or overnight.
Overnight culture (50 mL) is used to inoculate 1 L of 2xYT in a 4 L shaker flask. Bacteria are cultured in the flask to an OD600 of about 0.7, at which time IPTG is added to the culture to a final concentration of 1 mM. After a 4 h induction, bacterial pellets are collected by centrifugation and saved for subsequent protein purification.

[0290] Bacterial fermentation is performed under fed-batch conditions in a 10-liter fermentor.
One liter of complex fermentation medium contains 5 g of yeast extract, 20 g of tryptone, 0.5 g of NaCl, 4.25 g of KH2PO4, 4.25 g of K2HP04.3H20, 8 g of glucose, 2 g of MgSO4.7H2O, and 3 mL of trace metal solution (2.7% FeC13.6H2O/0.2% ZnC12.4H2O/0.2%
CoC12.6H2O/0.15%
Na2Mo04.2H2O/0.1% CaC12.2H2O/0.1% CuC12/0.05% H3BO3/3.7% HCI). The fermentor is inoculated with an overnight culture (5% vol/vol) and grown at constant operating conditions at pH 6.9 (controlled with ammonium hydroxide and phosphoric acid) and at 30 C.
The airflow rate and agitation are varied to maintain a minimum dissolved oxygen level of 40%. The feed (with 40% glucose) is initiated once the glucose level in the culture is belowlg /L, and the glucose level is maintained at 0.5 g/L for the rest of the fermentation. When the OD600 reaches about 60, IPTG is added into the culture to a final concentration of 0.05 mM.
Four hours after induction, the cells are harvested. The bacterial pellet is obtained by centrifugation and stored at -80 C for subsequent protein purification.

[0291 ] Expressed proteins that are soluble, secreted into the periplasm of the bacterial cell, and include an affinity tag (e.g., 6xHis tagged proteins) are purified using standard chromatographic methods, such as metal chelation chromatography (e.g., Ni affinity column), anionic/cationic affinity chromatography, size exclusion chromatography, or any combination thereof, which are well known to one skilled in the art.

[0292] Expressed proteins can form insoluble inclusion bodies in bacterial cells. These proteins are purified under denaturing conditions in initial purification steps and undergo a subsequent refolding procedure, which can be performed on a purification chromatography column. The bacterial pellets are suspended in a lysis buffer (0.5 M NaCl, 10mM Tris-HCI, pH 8, and 1 mM
EDTA) and sonicated. The inclusion body is recovered by centrifugation, and subsequently RECTIFIED SHEET (RULE 91) ISA/EP

dissolved in a binding buffer containing 6M guanidinium chloride, 50mM Tri-HCI, pH8, and 0.1M DTT. The solubilized portion is applied to a Ni affinitycolumn. After washing the unbound materials from the column, the proteins are eluted with an elution buffer (6M
guanidinium chloride, 50mM Tris-HCI pH8.0, 10mM 2-mercaptoethanol, 250mM imidazole).
Isolated proteins are buffer exchanged into the binding buffer, and are re-applied to the Ni' column to remove the denaturing agent. Once loaded onto the column, the proteins are refolded by a linear gradient (0-0.5M NaCI) using 5 C.V. (column volumes) of a buffer that lacks the denaturant (50mM Tris-HCI pH8.0, 10mM 2-mercaptoethanol, plus 2mM CaCI2). The proteins are eluted with a buffer containing 0.5M NaCl, 50mM Tris-HCI pH8.0, and 250mM imidazole.
The fusion tags (6xHis, CII6His) are cleaved with Factor Xa or Granzyme B, and removed from protein samples by passage through a Ni+-NTA affinity column. The proteins are further purified by ion-exchange chromatography on Q-sepharose (GE) using linear gradients (0-0.5M
NaCl) over 10 C. V. in a buffer (50mM Tris-HCI, pH8.0 and 2mM CaCl2). Proteins are dialyzed into I XPBS
buffer. Optionally, endotoxin is removed by passing through a Mustang E filter (PALL).
[0293] To prepare soluble extracts from bacterial cells for expressed proteins in the periplasm, the bacterial pellets are suspended in a loading buffer (10mM phosphate buffer pH6.0), and lysed using sonication (or alternatively a French press). After spinning down the insoluble portion in a centrifuge, the soluble extract is applied to an SP FF column (GE).
Periplasmic extracts are also prepared by osmotic shock or "soft" sonication. Secreted soluble 6xHis tagged proteins are purified by Ni+-NTA column as described above. Crude extracts are buffer exchanged into an affinity column loading buffer, and then applied to an SP FF column. After washing with 4 C. V.
of loading buffer, the proteins are eluted using a 100% gradient over 8 C.V.
with a high salt buffer (10mM phosphate buffer, 0.5M NaCl, pH6.0). Eluate is filtered by passing through a Mustang E filter to remove endotoxin. The partially purified proteins are buffer exchanged into 10mM phosphate buffer, pH7.4, and then loaded to a Q FF column. After washing with 7 C.V.
with 10mM phosphate buffer pH 6.0, the proteins are eluted using a 100%
gradient over 8 C.V.
with a high salt buffer (10mM phosphate buffer, pH6.0, 0.5M NaCI). Once again endotoxin is removed by passing through a Mustang E filter.

[02941 Example 14 RECTIFIED SHEET (RULE 91) ISA/EP

[0295] Expression and purification of TRAIL receptor agonists from mammalian cells [0296] Plasmids for each expression construct are prepared using a Qiagen Endofree Maxi Prep Kit. Plasmids are used to transiently transfect HEK293-EBNA cells. Tissue culture supernatants are collected for protein purification 2-4 days after transfection.

[0297] For large-scale production, stable cell lines in CHO or PER.C6 cells are developed to overexpress TRAIL receptor agonists. Cells (5x108) are inoculated into 2.5 L
of media in a 20 L
bioreactor (Wave). Once the cells have doubled, fresh media (lx start volume) is added, and continues to be added as cells double until the final volume reaches 10 L. The cells are cultured for about 10 days until cell viability drops to 20%. The cell culture supernatant is then collected for purification.

[0298] Both His-tagged protein purification (by Ni+-NTA column) and non-tagged protein purification (by ion exchange chromatography) are employed as detailed above.

[0299] Example 15 [0300] Affinity maturation of TRAIL receptor agonists assisted by in silico modeling [0301 ] In silico modeling is used to affinity mature TRAIL receptor agonists that are identified from the CTLD phage display library screening. Agonist homology models are built based on the known tetranectin 3D structures. Loop conformations of homology models of agonists are refined and optimized using LOOPER (DS2. 1, Accelrys) and their related algorithms. This process includes three basic steps: 1. Construction of a set of possible loop conformers with optimized interactions of loop backbone with the rest of the protein; 2.
Building and structural optimization of loop side chains and energy minimization applied to all loop atoms; 3. Final scoring and ranking the retained variants of loop conformers. Potential binding regions or epitopes located on the DR4/DR5 extracellular domain are identified for the agonists using a.
combination of manual and molecular dynamics-based docking. The binding domains are further confirmed by performing binding assays using deletion or point mutations of DR4/DR5 extracellular domain(s) and the agonists. Amino acid residues (or sequences) that are involved in determining binding specificity are defined on both DR4/DR5 and TRAIL CTLD
agonists. A
combination of random mutations at various target positions is screened using structure-based RECTIFIED SHEET (RULE 91) ISA/EP

computation to determine the compatibility with the structure template. Based on the analysis of apparent packing defects, residues are selected for mutagenesis to construct a library for phage display.

[0302] The 3D models of TRAIL receptor agonist peptides and DR4/DR5 can be used as a reference to refine the peptide-grafted CTLD and DR4/DR5 modeling. When TRAIL
receptor agonist peptides are grafted into CTLD loops, loop conformations are optimized and re-surfaced to match agonist peptides/DR4/DR5 binding by changing the flanking and surrounding amino acid residues using in silico modeling. Peptide grafted CTLD agonist homology models are built based on the known tetranectin 3D structures. Loop conformations of homology models of agonists are refined and optimized using LOOPER (DS2.1, Accelrys) and their related algorithms as described above. A combination of random mutations at various target positions is screened by structure-based computation for their compatibility with the structure template. Based on analysis of apparent packing defects, amino acid residues flanking and surrounding peptides are selected for mutagenesis to construct a library for phage display.
[0303] Example 16 [0304] Inhibition of cancer cell proliferation [0305] Human cancer cell lines expressing DR4 and/or DR5 such as COL0205 (colorectal adenocarcinoma), NCI-H2122 (non-small cell lung cancer), MIA PaCa-2 (pancreatic carcinoma), ACHN (renal cell carcinoma), WM793B (melanoma) and U266B1 (lymphoma) (all purchased from American Type Tissue Collection (Manassas, VA) are cultured under the appropriate condition for each cell line and seeded at cell densities of 5,000-20,000 cells/well (as determined appropriate by growth curve for each cancer cell line). DR4/5 agonistic molecules are added at concentrations ranging from 0.0001-100 g/mL. Optionally DR4/DR5 agonists are combined with therapeutic methods, including chemotherapeutics (e.g., bortezomib) or cells that are pre-sensitized by radiation, to generate a synergistic effect that upregulates DR4 or DR5 or alters caspase activity. The number of viable cells is assessed after 24 and 48 h using "CellTiter 96 AQõ,~,õs One Solution Cell Proliferation Assay" (Promega) according to the manufacturer's instructions, and the IC50 concentrations for the DR4/DR5 agonists are determined.

RECTIFIED SHEET (RULE 91) ISA/EP

[0306] Example 17 [0307] Activation of caspases by DR5 and DR4 agonistic molecules in cancer cell lines [0308] Human cancer cell lines expressing DR4 and/or DR5 such as COL0205 (colorectal adenocarcinoma), NCI-H2122 (non-small cell lung cancer), MIA PaCa-2 (pancreatic carcinoma), ACHN (renal cell carcinoma), WM793B (melanoma) and U266B1 (lymphoma) (all purchased from American Type Tissue Collection (Mannasas, VA)) are cultured under the appropriate condition for each cell line and seeded at cell densities of 5,000-20,000 cells/well (as determined appropriate by growth curve for each cancer cell line). DR4/5 agonistic molecules are added at concentrations ranging from 0.0001-100 pg/mL. DR4/DR5 agonists can be combined with other therapies such as chemotherapeutics (e.g., bortezomib) or cells that are pre-sensitized by radiation to determine whether such a combination has a synergistic effect on up-regulation of DR4 or DR5 or altering caspase activity. Caspase activity is determined at various timepoints using the "APO-ONE Caspase assay" (Promega) according to the manufacturers instruction.
[0309] Further analysis by Western Blot is performed by incubating 2x 106 tumor cells as described above. Subsequent cell lysates are prepared for Western Blot.
Proteins are separated by SDS-PAGE and transferred to nitrocellulose membranes. The filters are incubated with antibodies that recognize the pro and cleaved forms of the apoptotic proteins PARP, caspase 3, caspase 8, caspase 9, bid and actin. The bands corresponding to specific proteins are detected by HRP-conjugated secondary antibodies and enhanced chemiluminescence.

[0310] Example 18 [0311 ] Agonist molecule assessment in tumor xenograft models [0312] Cancer cell lines (e.g. HCT-116, SW620, COLO205) are injected s.c into Balb/c nude or SCID mice. Tumor length and width is measured twice a week using a caliper.
Once the tumor reaches 250 mm3 in size, mice will be randomized and treated i.v. or s.c. with 10-100 mg/kg DR4 or DR5 agonist. Treatment can be combined with other therapeutics such as chemotherapeutics (e.g. irinotecan, bortezomib, or 5FU) or radiation treatment. Tumor size is observed for 30 days unless tumor size reaches 1500 mm3 in which case mice have to be sacrificed.

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[0313] Example 19 [0314] Panning of human library 1-4 on human DR4 and DR5 [0315] 1. Panning on DR4 receptor [0316] Panning was performed using the human Loopl-4 library of human CTLDs on DR4/Fc antigen-coated (R&D Systems) wells prepared fresh the night before bound with 250 ng to 1 g of the carrier free target antigen diluted in 100 gL of PBS per well. Antigen plates were incubated overnight at 4 C then for 1 hour at 37 C, washed twice with PBS/0.05% Tween 20 and twice with PBS, and then blocked with 1% BSA/PBS for 1 hr at 37 C prior to panning. Six wells were used in each round, and phage were bound to wells for two hours at 37 C using undiluted, 1:10, and 1:100 dilutions in duplicates of the purified phage supernatant stock. Since target antigens were expressed as Fc fusion proteins, phage supernatant stocks contained 1 gg/mL soluble IgGI Fc acting as soluble competitor. In addition, prior to target antigen binding, phage supernatants were pre-bound to antigen wells with human IgGI Fc to remove Fc binders (no soluble IgG 1 Fc competitor was present during the pre-binding).

[0317] To produce phage for the initial round of panning, 10 g of library DNA
was transformed into electrocompetent TG-1 bacteria and grown in a 100 mL culture containing SB with 40 gg/mL carbenicillin and 2% glucose for 1 hour at 37 C. The carbenicillin concentration was then increased to 50 g/mL and the culture was grown for an additional hour.
The culture volume was then increased to 500 mL, and the culture was infected with helper phage at a multiplicity of infection (MOI) of 5x109 pfu/mL and grown for an additional hour at 37 C. The bacteria were spun down and resuspended in 500 mL SB containing 50 jig/mL
carbenicillin and 100 gg/mL kanamycin and grown overnight at room temperature shaking at 250 rpm. The following day bacteria were spun out and the phage precipitated with a final concentration of 4%
PEG/0.5 M NaCI on ice for 1 hr. Precipitated phage were then spun down at 10,500 rpm for 20 minutes at 4 C. Phage pellets were resuspended in 1% BSA/PBS containing the Roche EDTA
free complete protease inhibitors. Resuspended phage were then spun in a microfuge for 10 minutes at 13,200 rpm and passed through a 0.2 M filter to remove residual bacteria.

[0318] 50 gL of the purified phage supernatant stock per well were pre bound to the IgG Fc RECTIFIED SHEET (RULE 91) ISA/EP

coated wells for 1 hr at 37 C and then transferred to the target antigen coated well at the appropriate dilution for 2 hrs at 37 C as described above. Wells were then washed with PBS/0.05% Tween 20 for 5 minutes pipeting up and down (1 wash at round 1, 5 washes at round 2, and 10 washes at rounds 3 and 4). Target antigen bound phage were eluted with 60 L per well acid elution buffer (glycine pH 2) and then neutralized with 2M Tris 3.6 L/well. Eluted phage were then used to infect TG-1 bacteria (2 mL at OD600 of 0.8-1.0) for 15 minutes at room temperature. The culture volume was brought up to 10 mL in SB with 40 g/mL
carbenicillin and 2% glucose and grown for 1 hour at 37 C shaking at 250 rpm. The carbenicillin concentration was then increased to 50 g/mL and the culture was grown for an additional hour.
The culture volume was then increased to 100 mL, and the culture was infected with helper phage at an MOI of 5x109 pfu/mL and grown for an additional hour at 37 C. The bacteria were spun down and resuspended in 100 mL SB containing 50 g/mL carbenicillin and 100 g/mL
kanamycin and grown overnight at room temperature with shaking at 250 rpm.
Subsequent rounds of panning were performed similarly adjusting for smaller culture volumes, and with increased washing in later rounds. Clones were panned on DR4/Fc for four rounds and clones obtained from screening rounds three and four.

[0319] 2. Phage ELISA

[0320] Panning was performed using the TG-1 strain of bacteria for at least four rounds. At each round of panning sample titers were taken and plated on LB plates containing 50 g/mL
carbenicillin and 2% glucose. To screen for specific binding of phagemid clones to the receptor target, individual colonies were picked from these titer plates from the later rounds of panning and grown up overnight at room temperature with shaking at 250 rpm in 250 L
of 2xYT
medium containing 2% glucose and 50 gg/mL carbenicillin in a polypropylene 96-well plate with an air-permeable membrane on top. The following day a replica plate was set up in a 96-deep-well plate by inoculating 500 L of 2xYT containing 2% glucose and 50 g/mL
carbenicillin with 30 L of the previous overnight culture. The remaining overnight culture was used to make a master stock plate by adding 100 L of 50% glycerol to each well and storing at -80 C. The replica culture plate was grown at 37 C with shaking at 250 rpm for approximately 2 hrs until the OD600 was 0.5-0.7. The wells were then infected with K07 helper phage to 5x109 pfu/mL mixed and incubated at 37 C for 30 minutes without shaking, then incubated an addition RECTIFIED SHEET (RULE 91) ISA/EP

30 minutes at 37 C with shaking at 250 rpm. The cultures were then spun down at 2500 rpm and 4 C for 20 minutes. The supernatants were removed from the wells and the bacterial cell pellets were re-suspended in 500 L of 2xYT containing 50 gg/mL carbenicillin and 50 g/mL
kanamycin. An air-permeable membrane was placed on the culture block and cells were grown overnight at room temperature with shaking at 250 rpm.

[0321 ] On day 3, cultures were spun down and supernatants containing the phage were blocked with 3% milk/PBS for 1 hr at room temperature. An initial Phage ELISA was performed using 75-100 ng of antigen bound per well. Non-specific binding was measured using 75-100 ng of human IgGI Fc per well. DR4/Fc antigen (R&D Systems)-coated wells and IgG Fc coated wells were prepared fresh the night before by binding the above amount of antigen diluted in 100 gL
of PBS per well. Antigen plates were incubated overnight at 4 C then for 1 hour at 37 C, washed twice with PBS/0.05% Tween 20 and twice with PBS, and then blocked with 3%
milk/PBS for 1 hr at 37 C prior to the ELISA. Blocked phage were bound to blocked antigen-bound plates for 1 hr then washed twice with 0.05% Tween 20/PBS and then twice more with PBS. A HRP-conjugated anti-M13 secondary antibody diluted in 3% milk/PBS was then applied, with binding for 1 hr and washing as described above. The ELISA signal was developed using 90 L TMB substrate mix and then stopped with 90 L 0.2 M sulfuric acid, then ELISA plates were read at 450 nM. Secondary ELISA screens were performed on the positive binding clones identified, screening against additional TRAIL receptors and decoy receptors to test for specificity (DR4, DR5, DcR 1 and DcR2). Secondary ELISA screens were performed similarly to the protocol detailed above.

[0322] DR4 specific binding clones. Examples of amino acid sequences for Loops 1 and 4 selected for specific binding to the DR4 receptor from the human TN 1-4 library are detailed below in Table 5.

RECTIFIED SHEET (RULE 91) ISA/EP

Table 5 Sequences of Loops I and 4 from binders to human DR4 Loop 1 Loop I Loop 4 Loop 4 Clones Sequence SEQ Sequence SEQ ID
ID NO NO

014-42.3D11 GWLEGAGW 218 DGGWHWRWEN 219 014-42.3B8 GWLEGVGW 220 DGGEHWGWEN 221 014-42.3D9 GYLAGVGW 222 DGGRGFRWEN 223 014-42.3C7 GWLEGYGW 224 DGGTWWEWEN 225 014-42.3D 10 GYLEGYGW 226 DGGATIAWEN 227 014-42.3G8 GWLEGVGW 228 DGGRGWPWEN 229 014-40.3E11 GYLAGYGW 230 DGGPSIWREN 231 014-40.3B2 GYIEGTGW 232 DGGSNWAWEN 233 014-40.3B3 GYMSGYGW 234 DGGMMARWEN 235 014-40.3A3 GFMVGRGW 236 DGGSMWPWEN 237 014-40.3H2 MVTRPPYW 238 DGGWVMSFEN 239 014-40.3E9 PFRVPgWW 240 DGGYGPVGEN 241 064-40.2G1I GWLEGAGW 218 DGGWOWRWEN 242 064-40.2E10 GYLDGVGW 243 DGGQGCRWEN 244 064-36.1E4 VLRLAWSW 245 DGGKRNGCEN 246 064-40.1 E 1I WLSLFSPW 247 DGGRGVRGEN 248 064-36.1B7 GWMAGVGW 249 DGGRRLPWEN 250 064.40.2C7 SYRLHYGW 251 DGGRRWLGEN 252 064-36.1EI IWPLRFRW 253 DGGFVTRKEN 254 064-40.2D9 WgLYYRYW 255 DGGVGCMVEN 256 064-36.1G4 RCLgGVGW 257 DGGRGWPWEN 229 064-36.1E12 GCTgGQGW 258 DGGKKWKWEN 259 064-21.1A5 GFLgGNGW 260 DGGMWDRWEN 261 064-40.2A10 GVLgRGGW 262 DGGPGGEREN 263 064-40.2C3 PFRVLgOWW 264 DGGCGPV EN 265 064-40.2D2 PFRGPQQWW 266 DGGYGPVGEN 267 064-40.2E5 ARFAMWQQW 268 DGGRAGVGEN 269 064-40.2Q4 GWLEGYGW 270 DGG IgQ GWGEN 271 RECTIFIED SHEET (RULE 91) ISA/EP

064-40.2C5 AWRSWLNW 272 DGGREgQRREN 273 029-61.1E11 GWLEGVGW 220 DGGWPFSNEN 274 029-61.1A5 GWLMGTGW 275 DGGVVWNRWEN 276 029-62.2C5 VRRMGFHW 277 DGGRVAVGEN 278 029-62.2B3 RYHVOALW 279 DGGRVRPREN 280 029-62.4F5 IgCSPPLW 281 DGGAV EN 282 029-62.7D10 GLAROaGW 283 DGGKGRPREN 284 064-40.1G9 GWLSGVGW 285 DGGWAHAWEN 286 064-40.1C7 GWLEGVGW 220 DGGGGVRWEN 287 064-98.1G6 GWLSGYGW 288 DGGRVWSWEN 289 064-99.2H5 GLLSDWWW 290 DGGGNgSREN 291 064-101.4B10 OWVAFWSW 292 DGGSAVSGEN 293 064-101.4H1 PYTSWGLW 294 DGGVGGRGEN 295 064-40.1GII VARWLLKW 296 DGGMCKPCEN 297 064-36.1E10 GFLAGVGW 298 DGGWWTRWEN 299 064-36.1 G 10 GYLOGSGW 300 DGGWKTRWEN 301 064-36.1D7 VRHWLaLW 302 DGGGWWKGEN 303 [0323] 3. Panning on DR5 receptor [0324] Panning on the DR5 receptors was performed similarly to that detailed above for the DR4 receptor with the exception that five rounds of panning were performed and pre-binding was performed on wells coated with BSA rather than IgGI Fc. However phage supernatant stocks contained soluble IgG I Fc to act as soluble competitor for Fc binding during each round. DR5-specific binding clones were obtained screening from round 5. Amino acid sequences for Loops I and 4 obtained from the clones for DR5 specific binding are shown below in Table 6, below.

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Table 6 Sequences of Loops I and 4 from binders to human DR5 Loop I Loop 1 Loop 4 Loop 4 Clone SEQ SEQ ID
Sequence Sequence ID NO NO
029-15.A3C RATLRPRW 304 DGG----KN 305 029-15.A7D RAMLRSRW 306 DGGRWFOGKN 307 029-15.A5A RALFRPRW 308 DGGPWYLKEN 309 029-15.AIH RAVLRPRW 310 DGGWVLGGKN 311 029-15.A8G RAWLRPRW 312 DGGTLVSGEN 313 029-15.B10A RVIRRSMW 314 DGGOKWMAEN 315 029-15.B2H RVLORPVW 316 DGGMVWSMEN 317 029-15.B12H RVgLRPRW 318 EGGFRRHAKN 319 029-15.A6C RVVRLSEW 320 DGGMLWAMEN 321 029-15.B3G RVISAPVW 322 DGG WAMEN .323 029-15.BI2G RVLRRPOW 324 NGGDWRIPEN 325 029-15.A6B RVMMRPRW 326 DGGMWGAMEN 327 029-15.B4F RVMRRVLW 328 DGGRRETMKN 329 029-15.A9G RVMRRPLW 330 DGGRGOOWEN 331 029-15.B11F RVMRRREW 332 DGAOL MALEN 333 029-15.B11C RVWRRSLW 334 DGGHLVKOKN 335 029-15.A4G KRRWYGGW 336 DGGVNTVREN 337 029-15.B9F KRVWYRGW 338 DGGMRRRREN 339 029-15.A9B AVIRRPLW 340 DGGMKYTMEN 341 029-15.B4H ELVTSRLW 342 DGGVMgLGEN 343 029-15.B11G ELGTSRLW 344 DGGVMgLGEN 343 029-15.B3A FRGWLRWW 345 DDGARVLAEN 346 029-15.B1A GRLKGIGW 347 DGGRPOWGEN 348 029-15.A4E GVWgSFPW 349 DGGLGYLREN 350 029-15.B3E HLVSLAPW 351 DGGGMHOGKN 352 029-15.A1 1H HIFIDWGW 353 DGGVMTMGEN 354 029-15.B4D PVMRGVTW 355 DGGRSWVWEN 356 029-15.A2E OLVTVGPW 357 DGGVM14RTEN 358 RECTIFIED SHEET (RULE 91) ISA/EP

029-15.A7F OLVVgMGW 359 DGGWMTVGEN 360 029-15.B11A VAIRRSVW 361 DGGERAHSEN 362 029-15.B2B WVMRRPLW 363 DGGSMGWREN 364 029-15.A8E WRSMVVWW 365 DGGKHTLGEN 366 029-15.B3D ELRTDGLW 367 DGGVMRRSEN 368 [0325] As stated above, Loop 1 contained seven randomized amino acids in the screened library, whereas Loop 4 had an insertion of 5 randomized amino acids in place of 2 native amino acids (underlined regions in Table 6). In some clones having a glutamine (Q) in an altered loop, an amber-suppressible stop codon (TAG) encoded the glutamine, and this is indicated by a lower case "q". During panning, a few clones containing changes outside of these regions were identified, for example, in Loop 4, the carboxy-flanking amino acid has been altered from E to K
in several instances.

[0326] Example 20 [0327] Subcloning and production of ATRIMERTM binders to human DR4 and DR5 receptors [0328] The loop region DNA fragments were released from DR4/DR5 binder DNA by double digestion with Bg1II and Mfel restriction enzymes, and were ligated to bacterial expression vectors pANA4 (SEQ ID: 54), pANA10 (SEQ ID NO: 60) or pANA19 to produce secreted ATRIMERTM in E. coll.

[0329] The expression constructs were transformed into E. coli strains BL21 (DE3), and the bacteria were plated on LB agar with ampicillin. Single colony on a fresh plate was inoculated into 2xYT medium with ampicillin. The cultures were incubated at 37 C in a shaker at 200 rpm until OD600 reached 0.5, then cooled to room temperature. Arabinosis was added to a final concentration of 0.002-0.02%. The induction was performed overnight at room temperature with shaking at 120-150 rpm, after which the bacteria were collected by centrifugation. The periplasmic proteins were extracted by osmotic shock or gentle sonication.

[0330] The 6xHis-tagged ATRIMERsTM were purified by Ni+-NTA affinity chromatography.
Briefly, periplasmic proteins were reconstituted in a His-binding buffer (100 mM HEPES, pH

RECTIFIED SHEET (RULE 91) ISA/EP

8.0, 500 mM NaCl, 10 mM imidazole) and loaded onto a Ni+-NTA column pre-equivalent with His-binding buffer. The column was washed with l OX vol. of binding buffer.
The proteins were eluted with an elution buffer (100 mM HEPES, pH 8.0, 500 mM NaCl, 500 mM
imidazole). The purified proteins were dialyzed into PBS buffer and bacterial endotoxin was removed by anion exchange.

[0331] The strep II-tagged ATRIMERsTM were purified by Strep-Tactin affinity chromatography. Briefly, periplasmic proteins were reconstituted in IX binding buffer (20 mM
Tris-HCI, pH 8.5, 150 mM NaCl, 2 mM CaCl2i 0.1% Triton X-100) and loaded onto a Strep-Tactin column pre-equivalent with binding buffer. The column was washed with 1 OX vol. of binding buffer. The proteins were eluted with an elution buffer (binding buffer with 2.5 mM
desthiobiotin). The purified proteins were dialyzed into binding buffer and bacterial endotoxin was removed by anion exchange.

[0332] The DNA fragments of loop region were sub-cloned into mammalian expression vectors pANA2 (SEQ ID NO: 52) and pANAl I (SEQ ID NO: 61) to produce ATRIMERsTM in a HEK293 transient expression system. The DNA fragments of the loop region were released from IL-23R binder DNA by double digestion with BglII and Mfel restriction enzymes, and ligated to the expression vectors pANA2 and pANA11, which were pre-digested with Bg11I
and MfeI. The expression plasmids were purified from bacteria by Qiagen HiSpeed Plasmid Maxi Kit (Qiagene). For HEK293 adhesion cells, the transient transfection was performed by Qiagen SuperFect Reagent (Qiagene) according to the manufacturer's protocol. The day after transfection, the medium was removed and changed to 293 Isopro serum-free medium (Irvine Scientific). Two days later, 20% glucose in 0.5M HEPES was added into the media to a final concentration of 1%. The tissue culture supernatant was collected 4-7 days after transfection for purification. For HEK293F suspension cells, the transient transfection was performed by Invitrogen's 293 Fectin and its protocol. The next day, IX volume of fresh medium was added into the culture. The tissue culture supernatant was collected 4-7 days after transfection for purification. The His- or Strep II-tagged ATRIMERTM purification from mammalian tissue culture supernatant was performed as described above.

[0333] The DNA fragments of loop region were sub-cloned into mammalian expression vectors RECTIFIED SHEET (RULE 91) ISA/EP

pANA5 (SEQ ID NO: 55), pANA6 (SEQ ID NO: 56), pANA7 (SEQ ID NO: 57), pANA8 (SEQ
ID NO: 58) and pANA9 (SEQ ID NO: 59) to produce ATRIMERTM complexes with different CTLD-presenting orientations in the HEK293 transient expression system. pANA5 is a modified pCEP4 vector containing a C-terminal His-tag and a V49 deletion in human TN.
Similarly, pANA6 has a T48 deletion, and pANA7 has T48 and V49 deletions. pANA8 has a C50,C60-*S50,S6o double mutation to provide a more flexible CTLD than wildtype TN. pANA9 has E1-deletions to remove the glycosylation site. The DNA fragments of loop region were released from IL-23R binder DNA by double digestion with BglII and Mfel restriction enzymes, and were ligated to the expression vectors pANA5, pANA6, pANA7, pANA8 and pANA9, which were pre-digested with BglII and Mfel.

[0334] Example 21 [0335] Characterization of the affinity of human DR4 and DR5 receptor binders using Biacore [0336] Apparent affinities of the trimeric DR4 and DR5 binders are provided in Tables 7 and 8, respectively. Immobilization of an anti-human IgG Fc antibody (Biacore) to the CM5 chip (Biacore) was performed using standard amine coupling chemistry and this surface was used to capture recombinant human DR4 or DR5 receptor Fc fusion protein (R&D Systems).
ATRIMERTM COMPLEX dilutions (1-500 nM) were injected over the IL-23 receptor surface at 30 l/min and kinetic constants were derived from the sensorgram data using the Biaevaluation software (version 3.1, Biacore). Data collection was 3 minutes for the association and 5 minutes for dissociation. The anti-human IgG surface was regenerated with a 30s pulse of 3 M
magnesium chloride. All sensorgrams were double-referenced against an activated and blocked flow-cell as well as buffer injections.

Table 7 Apparent affinities of DR4 receptor binders from H Loop 1-4 library.
Analyte K. (1/M-s) Kd (1/s) KA (1/M) KD (nM) 014-42.3D10 1.22E+04 1.85E-03 6.58E+06 152 014-42.3B8 1.12E+05 1.01 E-03 1.11 E+08 9.01 014-42.3D11 1.33E+04 5.26E-04 2.53E+07 39.5 RECTIFIED SHEET (RULE 91) ISA/EP

Table 8 Apparent affinities of DR5 receptor binders from H Loop 1-4 library.
Analyte K. (1/M=s) Kd (1/s) KA (1/M) Kp (nM) la7b (=A8G) 4.05E+04 6.29E-04 6.43E+07 15.6 8b6b (=AIH) 1.29E+04 5.06E-04 2.56E+07 39.1 9b3d (=13313) 116 1.04E-04 1.11E+06 899 2al a (=139F) 4.38E+04 1.84E-03 2.38E+07 42.8 4a8c (=A3C) 6.30E+04 3.62E-04 1.74E+08 5.74 [0337] Description of cell assay.

[0338] H2122 lung adenocarnoma cells (ATCC# CRL-5985) and A2780 ovarian carcinoma cells (European Collection of Cell Culture, #93112519) were incubated at 1 x 104 cells/well with DR5 ATRIMERsTM (20 gg/mL) or TRAIL (0.2 g/mL, R&D Systems) in 10% FBS/RMPI media (Invitrogen) in a 96-well white opaque plate (Costar). The control wells received media and the respective buffer: TBS for DR5 ATRIMERsTM and PBS for TRAIL. After 20 hours, cell viability was determined by ViaLight Plus (Lonza) and detected on a Glomax luminometer (Promega).
Data were expressed as percent cell death relative to the respective buffer control. (See FIG. 10).
The mean and standard error of triplicates were plotted using Excel. Five DR5 ATRIMERTM
COMPLEX were tested: 4a8c, 2a1 a, 1 alb, 9b3d and 8b6b. Three DR5 ATRIMERsTM
(4a8c, 1 alb and 8b6b) showed over 50% killing in both cell lines. Similar data were obtained in a separate experiment.

[0339] Example 22 [0340] Panning of NEB peptide libraries on human DR5 and identification of a DR5 specific peptide [0341] Panning of peptide libraries was performed using the New England Biolabs (NEB) Ph.D.
Phage Display Libraries. Panning was performed on DR5/Fc antigen-coated (R&D
Systems) RECTIFIED SHEET (RULE 91) ISA/EP

wells prepared fresh the night before bound with 3 pg of the carrier free target antigen diluted in 150 L of 0.1M NaHCO3 pH 8.6 per well. Duplicate wells were used in each round. Antigen plates were incubated overnight at 4 C then for 1 hour at 37 C. The antigen was removed and the well was then blocked with 0.5% boiled Casein in PBS pH 7.4 for 1 hr at 37 C prior to panning. The Casein was then removed and wells were then washed 6X with 300 gL
of TBST
(0.1 % Tween), then phage were added. Since target antigens were expressed as Fc fusion proteins, prior to target antigen binding, phage supernatants were pre-bound for 1 hr to antigen wells with human IgGI Fc to remove Fc binders (during rounds 2 through 4 ). Fc antigen bound wells were prepared similar to DR5/Fc antigen bound wells as detailed above.

[0342] For the initial round of panning, 100 L of TBST(0.1 % Tween) was added to each well and 5 ul of each of the 3 NEB peptide libraries (Ph.D.-7, Ph.D.-12, and Ph.D.-C7C) were added to each well. The plate was rocked gently for 1 hr at room temperature, then washed l OX with TBST(0.1% Tween). Bound phage were eluted with 100 L of PBS containing soluble DR5/Fc target antigen at a concentration of 100 gg/ml. Phage were eluted for 1 hr rocking at room temperature. Eluted phage were then removed from the wells and used to infect 20 mls of ER2738 bacteria at an OD600,,,,, of 0.05 to 0.1, and grown shaking at 250 rpm at 37 C for 4.5 hrs.
Bacteria were then spun out of the culture at 12K X G for 20 min at 4 C.
Bacteria were transferred to a fresh tube and re-spun. The supernatant was again transferred to a fresh tube and the Phage were precipitated by adding 1/6th the volume of 20% PEG/2.5M NaCl.
Phage were precipitated overnight at 4 C. The following day the precipitated phage were spun down at 12K
X G for 20 min at 4 C. The supernatant was discarded and the phage pellet re-suspended in 1 ml of TBST(0. I% Tween). Residual bacteria were cleared by spinning in a microfuge at 13.2K for minutes at 4 C. The phage supernatant was then transferred to a new tube and re-precipitated by adding 1/6 1h the volume of 20% PEG/2.5M NaCl, and incubating at 4 C on ice for 1 hr. The precipitated phage were spun down in a microfuge at 13.2K for 10 minutes at 4 C. The supernatant was discarded and the phage pellet re-suspended in 200 L of TBS.
Subsequent rounds of panning were performed similar to round I with the exception phage were pre-bound for 1 hr to Fc coated wells and that 4 L of the amplified phage stock from the previous round were used per well during the binding. In addition the tween concentration was increased to 0.5% in the TBST used during the 10 washes.

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[0343] Phage ELISA

[0344] Panning was performed using the ER2738 strain of bacteria for at least four rounds. At each round of panning sample titers were taken and plated using top agar on LB/Xgal plates to obtain plaques. To screen for specific binding of phage clones to the receptor target, individual plaques were picked from these titer plates from the later rounds of panning and used to infect ER2738 bacteria at an OD600ni,, of 0.05 to 0.1, and grown shaking at 250 rpm at 37 C for 4.5 hrs.
Then stored at 4 C overnight.

[0345] On day 2, cultures were spun down at 12K X G for 20 min at 4 C, and supernatants containing the phage were blocked with 3% milk/PBS for 1 hr at room temperature. An initial Phage ELISA was performed using 75-100 ng of DR5/Fc antigen bound per well.
Non-specific binding was measured using wells containing 75-100 ng of human IgG I Fc petr well. DR5/Fc antigen (R&D Systems)-coated wells and IgG I Fc coated wells were prepared fresh the night before by binding the above amount of antigen diluted in 100 L of PBS per well. Antigen plates were incubated overnight at 4 C then for 1 hour at 37 C, washed twice with PBS/0.05% Tween 20 and twice with PBS, and then blocked with 3% milk/PBS for 1 hr at 37 C
prior to the ELISA.
Blocked phage were bound to blocked antigen-bound plates for 1 hr then washed twice with 0.05% Tween 20/PBS and then twice more with PBS. A HRP-conjugated anti-M13 secondary antibody diluted in 3% milk/PBS was then applied, with binding for 1 hr and washing as described above. The ELISA signal was developed using 90 L TMB substrate mix and then stopped with 90 pL 0.2 M sulfuric acid, then ELISA plates were read at 450 nM.
Secondary ELISA screens were performed on the positive binding clones identified, screening against additional TRAIL receptors and decoy receptors to test for specificity (DR4, DR5, DeR1 and DcR2). Secondary ELISA screens were performed similarly to the protocol detailed above.
[03461 DR5 specific binding clone. An example of the amino acid sequence of a peptide from the NEB Ph.D.-C7C phage library selected for specific binding to the DR
receptor is detailed below in Table 9.

RECTIFIED SHEET (RULE 91) ISA/EP

Table 9 Peptide Peptide Clone SEQ
Sequence ID NO
088-13.11-13 ACFPIMTLHCGGG 369 Table 10: TRAIL-Related Sequences Sequence Sequence SEQ ID
Description NO:
Human TRAIL MAMMEVQGGP SLGQTCVLIV IFTVLLQSLC VAVTYVYFTN
GenBank Acc. ELKQMQDKYS KSGIACFLKE DDSYWDPNDE ESMNSPCWQV

HSFLSNLHLR NGELVIHEKG FYYIYSQTYF RFQEEIKENT
KNDKQMVQYI YKYTSYPDPI LLMKSARNSC WSKDAEYGLY
SIYQGGIFEL KENDRIFVSV TNEHLIDMDH EASFFGAFLV G
DR4; TRAIL-RI MAPPPARVHL GAFLAVTPNP GSAASGTEAA AATPSKVWGS
GenBank Acc. SAGRIEPRGG GRGALPTSMG QHGPSARARA GRAPGPRPAR

LFACLPCTAC KSDEEERSPC TTTRNTACQC KPGTFRNDNS

WVILVVTLVV PLLLVAVLIV CCCIGSGCGG DPKCMDRVCF
WRLGLLRGPG AEDNAHNEIL SNADSLSTFV SEQQMESQEP
ADLTGVTVQS PGEAQCLLGP AEAEGSQRRR LLVPANGADP
TETLMLFFDK FANIVPFDSW DQLMRQLDLT KNEIDVVRAG
TAGPGDALYA MLMKWVNKTG RNASIHTLLD ALERMEERHA
KEKIQDLLVD SGKFIYLEDG TGSAVSLE

DR5; TRAIL-R2 MEQRGQNAPA ASGARKRHGP GPREARGARP GPRVPKTLVL
GenBank Acc. VVAAVLLLVS AESALITQQD LAPQQRAAPQ QKRSSPSEGL

PRGMVKVGDC TPWSDIECVH KESGTKHSGE APAVEETVTS

LPYLKGICSG GGGDPERVDR SSQRPGAEDN VLNEIVSILQ
PTQVPEQEME VQEPAEPTGV NMLSPGESEH LLEPAEAERS
QRRRLLVPAN EGDPTETLRQ CFDDFADLVP FDSWEPLMRK
LGLMDNEIKV AKAEAAGHRD TLYTMLIKWV NKTGRDASVH
TLLDALETLG ERLAKQKIED HLLSSGKFMY LEGNADSAMS

RECTIFIED SHEET (RULE 91) ISA/EP

Sequence Sequence SEQ ID
Description NO:

GenBank Acc. PQQQRHSFKG EECPAGSHRS EHTGACNPCT EGVDYTNASN

TPAAEETMNT SPGTPAPAAE ETMNTSPGTP APAAEETMTT
SPGTPAPAAE ETMTTSPGTP APAAEETMTT SPGTPASSITY
LSCTIVGIIV LIVLLIVFV

GenBank Acc. VVFIVAVLLP VRVDSATIPR QDEVPQQTVA PQQQRRSLKE

TILGMLASPY HYLIIIVVLV IILAVVVVGF SCRKKFISYL
KGICSGGGGG PERVHRVLFR RRSCPSRVPG AEDNARNETL
SNRYLQPTQV SEQEIQGQEL AELTGVTVES PEEPQRLLEQ
AEAEGCQRRR LLVPVNDADS ADISTLLDAS ATLEEGHAKE
TIQDQLVGSE KLFYEEDEAG SATSCL

OPG MNNLLCCALV FLDISIKWTT QETFPPKYLH YDEETSHQLL
GenBank Acc. CDKCPPGTYL KQHCTAKWKT VCAPCPDHYY TDSWHTSDEC

LCEEAFFRFA VPTKFTPNWL SVLVDNLPGT KVNAESVERI
KRQHSSQEQT FQLLKLWKHQ NKDQDIVKKI IQDIDLCENS
VQRHIGHANL TFEQLRSLME SLPGKKVGAE DIEKTIKACK
PSDQILKLLS LWRIKNGDQD TLKGLMHALK HSKTYHFPKT
VTQSLKKTIR FLHSFTMYKL YQKLFLEMIG NQVQSVKISC L

[0347] Examples 23- 32 provide exemplary methods for identifying and isolating CTLD
polypeptides that specifically bind IL-23 receptors using the combinatorial polypeptide libraries of the invention.

[0348] IL-23 is an essential cytokine for generation and survival of Th17 cells. There is mounting evidence from preclinical models and clinical experience that ThI7 cells play a critical role in pathology of many autoimmune diseases, including rheumatoid arthritis, inflammatory bowel disease, psoriasis, systemic lupus erythematosus (SLE) and multiple sclerosis. IL-23R is a key target on Th17 cells. Similarly, the IL-23 cytokine is composed of two subunits: p19 and RECTIFIED SHEET (RULE 91) ISA/EP

p40, with the p19 subunit being unique to IL-23, and p40 shared with IL-12.
The IL-23 receptor is a heterodimeric receptor that binds IL-23 and mediates activation of certain T cell subsets, NK
cells and myeloid cells. The IL-23 heterodimeric receptor is composed of two subunits: IL-23R
and IL-12R(31, with IL-23R being the subunit unique to the IL-23 pathway. IL-l2R(3l is shared with the IL-12 receptor and hence the IL-12 pathway.

[0349] Importantly, genetic variation in IL-23R has been associated with susceptibility to psoriasis and Crohn's disease and also has been implicated in susceptibility to ankylosing spondylitis, Vogt-Koyanagi-Harada disease, Systemic Sclerosis, Behcet's disease (BD), Primary Sjogren's Syndrome, Goodpasture disease. Also, importance of IL-23 in Graft Versus Host disease and chronic ulcers has been suggested, and IL-23 has been implicated in tumorigenesis.
[0350] Blockade of the IL-23 pathway is efficacious in many preclinical models of autoimmune disease. However, the nature of shared ligand and receptor subunits between IL-23 and IL- 12 pathways has led to more complex biology than previously appreciated, and separation of IL-23 blockade from IL- 12 blockade appears to have important therapeutic implications regarding both efficacy and safety. Blockade of one or the other, or both, can be done at the level of the cytokine subunits or the receptor subunits.

[0351 ] Example 23 [0352] Panning & Screening of human library 1-4 [0353] Phage generated from human library 1-4 were panned on recombinant human IL-23R/Fc chimera (R&D Systems), and recombinant mouse IL-23R/Fc chimera (R&D Systems).
Screening of these binding panels after three, four, and/or five rounds of panning using an ELISA plate assay identified receptor-specific binders in all cases.

[0354] To generate phage for panning, the master library DNA was transformed by electroporation into bacterial strain TG I (Stratagene). Cells were allowed to recover for one hour with shaking at 37 C in SOC (Super-Optimal broth with Catabolite repression) medium prior to increasing the volume 10-fold by adding super broth (SB) to a final concentration of 20% glucose and 20 g/mL carbenicillin. After shaking at 37 C for one hour, the carbenicillin concentration was increased to 50 g/mL for another hour, after which 400 mL
of SB with 2%

RECTIFIED SHEET (RULE 91) ISA/EP

glucose and 50 g/mL carbenicillin were added, along with helper phage Ml3K07 to a final concentration of 5x109 pfu/mL. Incubation was continued at 37 C without shaking for 30 minutes, and then with shaking at 100-150 rpm for another 30 min. Cells were centrifuged at 3200g at 4 C for 20 minutes, then resuspended in 500 mL SB medium containing 50 gg/mL
carbenicillin and 50 gg/mL kanamycin. Cells were grown overnight at room temperature (RT) with shaking at 150 rpm. Phage were isolated by pelleting the bacterial cells by centrifugation at 15,000 g and 4 C for 20 min. The supernatant was incubated with one-fourth volume (usually 250 mL of supernatant/bottle + 62.5 mL PEG solution) of 20% PEG/2.5 M NaCl on ice for 30 min. The phage is pelleted by centrifugation at 15,000 g and 4 C for 20 min.
The phage pellet was resuspended in 1% bovine serum albumin (BSA) in phosphate buffered saline (PBS) containing 0.1% sodium azide (BSA/PBS/azide) and complete mini-EDTA-free protease inhibitors (Roche), prepared according to the manufacturer's instructions.
Alternatively, phage was resuspended in Buffer D, containing 0.05% boiled cassein, 0.025% Tween-20, and protease inhibitors. Material was filter-sterilized using Whatman Puradisc 25 mm diameter, 0.2 pm pore size filters.

[0355] Phage generated from human library 1-4 were panned on recombinant human IL-23R/Fc chimera (R&D Systems cat #1686-MR). Library panning was performed either using a plate or a bead format. For the plate format, six to eight wells of a 96-well Immulon HB2 ELISA plate were coated with 250 -1000 ng/well of carrier-free human IL-23R/Fc in Dulbecco's PBS.
Material was incubated on the plate overnight, after which wells were washed three times with PBS, blocking buffer (either 1% BSA/PBS/azide or Buffer C, containing 0.05%
boiled casseing and 1% Tween-20) was added, and wells were then incubated for at least 1 hour at 37 C.
Additional wells were also treated with blocking buffer at the same time for later absorption of phage binding to blocking buffer.

[0356] Three dilutions of the phage preparation were used: undiluted, 1:10, and 1:100 in blocking buffer plus protease inhibitors. In some rounds of panning, recombinant human IgGI
Fc was added to each of the dilutions to a final concentration of 10 g/mL.
Blocking buffer was removed from the "Block Only" (preabsorption to block) wells and the different phage mixtures were incubated in these wells for another hour at 37 C. Aliquots (50 L) of each phage mixture were transferred to a washed and blocked target well and allowed to incubate for 2 h at 37 C. For RECTIFIED SHEET (RULE 91) ISA/EP

the first round of panning, bound phage were washed once with either I X
PBS/0.05% Tween or with Buffer D, and were eluted using glycine buffer, pH 2.2, containing I
mg/mL BSA. After neutralization with 2 M Tris base (pH 11.5) the eluted phage were incubated for 15 minutes at room temperature with two to four milliliters of TG1 (Stratagene), XL1-Blue (Stratagene), ER2738 (Lucigen or NEB), or SS320 (Lucigen) cells at an optical density of approximately 0.9 measured at 600 nm (OD600) in yeast extract-tryptone (YT) medium . Phage were prepared from this infection using the protocol above, but scaled down by about 20%
(volume). Phage prepared from eluted phage were subjected to additional rounds of panning. At each round, titers of input and output phage were determined by plating on agar with appropriate antibiotics, and colonies from these plates were used later for screening for binders by ELISA.

[0357] Additional rounds of panning were performed as described above, except that in the second round of panning, washes were increased to 5x, and in subsequent rounds, washes were increased to 10x. Three to six rounds of panning were performed. For the final round of panning, phage were not produced after infection; rather, infected bacteria were grown overnight and a maxiprep (Qiagen kit) was prepared from the DNA. Glycerol stocks (15%) of input phage were stored frozen (at -80 C) from each round.

[0358] For the bead panning format, human IL-23R was biotinylated and purified using a Sulfo-NHS micro biotinylation kit (Thermo-Scientific) according to the manufacturer's instructions.
Phage were generated for panning from the master library as per the protocol above, except that the phage pellet was resuspended in a casein buffer containing 0.5% boiled casein, 0.025%
Tween 20 in PBS with added EDTA-free protease inhibitors (Roche). Using a magnet, streptavidin magnetic beads (2 tubes with 50 gL or 0.5 mg each of Myone T1 Dynabeads (Invitrogen)) were washed several times in 0.5% boiled casein, I% Tween 20 to remove preservatives. A 150 L aliquot of the phage prep was preincubated with one tube of beads for 30 min at 37 C to remove streptavidin binders. The phage prep was then removed from the beads and I g of biotinylated IL-23R was added along with 10 L of human Fc at 100 gg/mL and incubated for 2 h at 37 C with rotation. This material was then added to the remaining tube of washed beads and incubated at 37 C for 30 min. Using the magnetic stand, beads were washed five times with PBS/0.05% Tween. Phage were eluted with glycine, pH 2.0, neutralized, and used to infect bacteria as described above. In subsequent rounds of panning, bead-bound phage RECTIFIED SHEET (RULE 91) ISA/EP

were washed ten times prior to elution. Titers of input and output phage were determined as described above.

[0359] For ELISA screening, colonies from later rounds of panning were grown in YT medium with 2% glucose and antibiotics overnight, and an aliquot of each was then used to start fresh cultures that were grown to an OD600 of 0.5. Helper phage were added to 5 x 109 pfu/mL and allowed to infect for 30 min at 37 C, followed by growth at 37 C with agitation. Bacteria were centrifuged and resuspended in YT medium with carbenicillin and kanamycin and grown overnight for phage production. Bacteria were then pelleted and the medium was removed and mixed with one-fifth volume (1:5 milk mixture: supernatant) of 6X PBS, 18%
milk. ELISA plates were prepared by incubating overnight at 4 C with 50-100 L of PBS containing 75-100 ng/well of recombinant human IL-23R/Fc. A duplicate plate coated with human IgG Fc (R&D Systems) was used as a control. Plates were washed 3 times with PBS, blocked for 1 h at 37 C with 3%
milk in I X PBS, and incubated for 1 hour with 100 uL/well of each milk-treated phage mixture.
Plates were washed once with PBS/0.05% Tween 20 and twice with PBS, incubated for one hour with an HRP-conjugated anti-M13 antibody (GE Healthcare), washed three times each with PBS/Tween and PBS, and incubated with TMB substrate (VWR). Sulfuric acid was added to stop the color reaction and absorbance was read at 450 nm to identify positive binders.

[0360] Binders to human IL-23R were identified from the third and fourth rounds of panning.
Examples of the sequences from the randomized regions of Loops I and 4 from phage-displayed CTLD binders to human IL-23R/Fc chimera are given in Table 11. Examination of these data suggests that for 31/36 of the binders, a motif was evident in the randomized region of Loop 4:
the second and fifth amino acids were always glycine, the fourth amino acid was always one of the cyclic amino acids tryptophan or phenylalanine, the first amino acid was hydrophobic, and usually a cyclic amino acid, such as phenylalanine, tyrosine, or tryptophan, and the third amino acid was hydrophobic, and was usually valine. The Loop I region had less of a consensus, though glycine and serine appeared predominantly in the first and second positions, and valine was often in the seventh position. Five additional binders did not appear to have this consensus, though two of these probably formed another small group, with MFGMG (SEQ ID
NO: 598) or LFGRG (SEQ ID NO: 599) in the Loop 4 region. Many binders were each represented by multiple clones.

RECTIFIED SHEET (RULE 91) ISA/EP

Sequences of human Loop I and 4 binders to human IL-23R/Fc chimera Clone ID Loop 1 Loop 1 Loop 4 Loop 4 Sequence SEQ ID NO Sequence SEQ ID NO
001-91.A1A GSNVTQT 376 FGAFG 377 001-91.A12C GSSVSDV 378 FGMWG 379 001-69.4H1 AGRYSLI 380 FGVFG 381 001-69.4G8 GSRRSGV 382 FGVFG 381 001-69.3E5 RGATVKV 383 FGVFG 381 001-87.A8E ANPAQDL 384 FGVWG 385 001-89.C3G APGAMEF 386 FGVWG 385 001-89.CIOB GSPDLGV 387 FGVWG 385 001-87.A5F GSVRSAT 388 FGYFG 389 001-91.A12E GSPVGDM 390 IGVWG 391 001-91.A7F GSSKLGL 392 IGVWG 391 001-69.4D4 GSVRGRT 393 IGVWG 391 001-69.3C2 TNVTRTL 394 LGVWG 395 001-87.A9E GSALTNT 396 LGYWG 395 001-89.C3C ANRRRTM 397 MGVWG 398 001-91.A7C GSSVSGL 399 VGVFG 400 001-69.4C6 GSWLGDV 401 VGVFG 400 001-89.C11E SGKARDV 402 VGVFG 400 001-91.A3D GSRFGHL 403 WGVFG 404 001-89.C3F GSRISGV 405 WGVFG 404 001-91.A6B SGKRRTV 406 WGVFG 404 001-89.C12C SGSWART 407 WGVFG 404 001-69.4C1 AGARAEY 408 WGVWG 409 001-69.4F2 GPGQAGL 410 WGVWG 409 001-91.A1B GSTYTDL 411 WGVWG 409 RECTIFIED SHEET (RULE 91) ISA/EP

001-69.4G3 GTRMTNT 412 WGYFG 413 001-89.C7F GSLLTGL 414 YGAWG 415 001-69.3H4 GSKAGKL 416 YGVFG 417 001-69.4C12 ASLRSRV 418 YGVWG 419 001-69.4E5 GNPSGSV 420 YGVWG 419 001-87.A3B TGALHQV 421 YGVWG 419 001-89. C 12E WTKRTAL 422 MFGMG 423 001-87.A4A WTLAKNL 424 LFGRG 425 001-69.4F5 VLGWRRE 426 LVMPM 427 001-69.3G5 LATWLRW 428 QRMSY 429 001-69.4F9 QHLGSFW 430 VEFQG 431 [0361 ] ELISA assays indicated that these binders did not cross-react with either human IgG I Fc or with recombinant mouse IL-23R. ELISA and Biacore binding assays indicated that purified monomeric CTLD or full-length trimers from candidate clones 001-69.4G8 and other competed with IL-23 for binding to the human IL-23R. Competitive candidates have been identified that have nanomolar affinities.

[0362] An example of a sequence from the randomized regions of Loops 1 and 4 from phage-displayed CTLD binders to mouse IL-23R/Fe is given in Table 12. This sequence has similarity to the primary motif seen in the human IL-23R binders (compare Loop 1, for example, to B12C, or Loop 4 to C12C). Interestingly, the invariant cyclic tryptophan/phenylalanine of position 4 in Loop 4 was replaced with glycine in the mouse IL-23R binder.

Sequences of human Loop I and 4 binders to mouse IL-23R
L Clone Loop 1 ISEQ ID NO] Loop 4 ISEQ ID NO]
H1-4P141D GSSQMDV [432] WGLGG [433]
[0363] Example 24 RECTIFIED SHEET (RULE 91) ISA/EP

[0364] Affinity maturation of binders to human IL-23R

[0365] Because the Loop 4 region of the human IL-23R appeared to be a relevant motif, a.
shuffling approach was developed preserving the diversity of Loop 4 regions already obtained by panning, but resorting them with all possible Loop 1 regions from the original naive library. To this end, DNA from the round 4 panning of human IL-23R was digested with EcoRI
and BssHll restriction enzymes, which cut between the Loop I and Loop 4 regions, and a fragment of about 1.4 kb, containing the Loop 4 region, was isolated. Separately, the original human 1-4 library DNA was digested with the same enzymes, and a fragment of about 3.5 kb, containing the Loop 1 region, was isolated. These fragments were ligated together and a new h1-4 shuffle library was generated as described above. The library was panned using the bead protocol (supra), except that at each round of panning the amount of biotinylated recombinant human IL-23RIFc was decreased about 10-fold, from 200 ng, (to 20 ng, to 2 ng) to 0.1 ng. Phage supernatants from colonies were screened by ELISA as described above and binders were identified and sequenced.
Loop 1 and 4 sequences of the affinity-matured binders appear in Table 13.

Loop I and 4 sequences from affinity-matured human Loop 1-4 binders to human Loop 1 Loop 1 Loop 4 Loop 4 Clone Sequence SEQ ID NO Sequence SEQ ID NO
056-40.A3C GSATTAT 434 FGYFG 389 056-45.F7F GSATTDT 435 FGYFG 389 056-41.B5C GSALTNT 396 FGYFG 389 056-53.H7H GSSVSDV 378 FGYFG 389 056-53.H4E GSALTNT 396 FGVFG 381 056-53.H1G SGHWRAV 436 FGVFG 381 056-42.C7D GSNVTQT 376 YGVFG 417 056-41.B12F GSVRSAT 388 YGVFG 417 056-41.B9B APPDLGL 437 WGVWG 409 056-42.C7F APKSRQY 438 FGVWG 385 105.
RECTIFIED SHEET (RULE 91) ISA/EP

056-44.E4G VMQLPRK 439 IGVWG 391 056-53.H7B AGRMGLV 440 WGVFG 404 [0366] A separate affinity maturation library was generated in which the diversity of the Loop I
regions obtained in the initial panning round 4 was maintained, a limited selection of Loop 4 options was utilized, and Loop 3 was randomized in six positions. This was achieved by generating primers to amplify the Loop 1 region using DNA from the original panning round 4 of the human Loop 1-4 library as template, along with primers Bglfor (SEQ ID
NO: 158) and HI -3-4R (SEQ ID NO: 185). This primer encodes the following amino acid sequence for loops 3 and 4:

[0367] RIAYKNWEXXXXXQPXGG(F/L)G(F/Y/V/D)(F/W/L/C)GENCAVLS (SEQ ID NO:
600).

[0368] This sequence incorporates the. primary alternatives for Loop 4, as well as alterations of the Loop 3 region of the CTLD. Other primers similar to this but more specific for the Loop 4 region sequences were also generated and used for production of another library randomized in the Loop 3 region. The remainder of the region of interest was generated by overlap PCR using primers PstLoop4rev (SEQ ID NO: 186) and Pst Rev (SEQ ID NO: 142).

[0369] Affinity matured IL-23R binding sequences obtained from these libraries are provided in Table 14. Some of the binders obtained were altered by swapping more favorable loop 4 or loop 1 sequences for others to obtain additional affinity-matured binders, and these are included in Table 14.

SEQ ID SEQ ID SEQ ID
Clone name Loop 1 NO Loop 3 NO Loop 4 NO

H4EWP1E9 GSALTNT 396 AGYTKQPS. 441 WGVFG 404 RECTIFIED SHEET (RULE 91) ISA/EP

101-51-1A$ GSALTNT 396 RTPPWQPE 455 FGYFG 389 101-80-5H3* GSALTNT 396 PPAPYHPM 460 -GVFG 461 [0370] *Clone 101-80-5H3 had an amino acid deleted from the planned loop 4 and two other amino acid changes (GlyGly to AlaAla) in the loop 4 region just upstream of the altered region.
[0371] Table 15 shows some additional clones that were made with a primer similar to H1-3-4R
(SEQ ID NO: 185), but having a coding sequences for the following loop modications.

SEQ ID SEQ ID SEQ ID
Clone name Loop 1 NO Loop 3 NO Loop 4 NO
079-86-P1D6h14 GSTLTRI 462 QEPAKQPT 443 FGAFG 377 [0372] Another affinity maturation library was generated by limiting loop 4 to five amino acid sequences: FGVFG (SEQ ID NO: 381), WGVFG (SEQ ID NO: 404), FGYFG (SEQ ID NO:
389), WGYFG (SEQ ID NO: 413), and WGVWG (SEQ ID NO: 409), while maintaining the GlySer found at the beginning of loop I in IL-23R binders, and varying the subsequent five amino acids in loop I using an NNK strategy. Primers GSXX (SEQ ID NO: 194) and BssBglrev (SEQ ID NO: 195) were mixed and extended using PCR, and primers FGVFGfor, FGYFGfor, WGVFGfor, WGYFGfor, and WGVWGfor (SEQ ID NOS: 196 to 200) were mixed individually with primer Pst Loop 4 rev (SEQ ID NO: 186) and extended using PCR. The resulting fragments were gel purified and mixed and extended by PCR in the presence of primers Bgl for (SEQ ID NO: 158) and Pst rev (SEQ ID NO: 142). The resulting fragments were digested with Bgl II and Pst I and inserted into vector pANA27 for phage display. Bead panning with successive target dilution was used to select affinity-matured candidates from the library.

RECTIFIED SHEET (RULE 91) ISA/EP

Sequences of the candidates obtained from this library are provided in Table 16.

Candidate LOOP 1 SEQ ID NO: LOOP 4 SEQ ID NO:

105-20-2C4a GSAKTDT 468 WGYFG 413 105-78-2.E6 GSLRTNT 492 FGVFG 381 RECTIFIED SHEET (RULE 91) ISA/EP

105-20-lB4 GSSRTNT 528 WGYFG 413 105-20-2C4b GSVKTDT 538 WGYFG 413 =105-55-1B9 GSVLTNT 541 FGYFG 389 RECTIFIED SHEET (RULE 91) ISA/EP

[0373] Additional changes in the amino acid sequences of the loops and surrounding sequences were generated by alanine scanning, i.e. the replacement of specific amino acids with the amino acid alanine by means of gene site specific mutagenesis, known to those skilled in the art. Table 17 describes the alanine replacements made in the candidate 056-53.H4E
sequence. Such replacements are not limited to the residues shown and can be made in any candidate backbone.
Table 17 shows that many of these replacements were beneficial for affinity and/or protein production.

Sequences of alanine scan candidates that bind IL-23R.
SEQ
ID
Candidate Sequence of AA 115 to 172* NO.
056-53.H4E NGSALTNTWVDMTGARIAYKNWETEITAQPDGGFGVFGENCAVLSGAANGKWFDKRCR 550 H4E E153A* NGSALTNTWVDMTGARIAYKNWETEITAQPDGGFGVFGANCAVLSGAANGKWFDKRCR 572 H4E N154A* NGSALTNTWVDMTGARIAYKNWETEITAQPDGGFGVFGEACAVLSGAANGKWFDKRCR 573 H4E R170A* NGSALTNTWVDMTGARIAYKNWETEITAQPDGGFGVFGENCAVLSGAANGKWFDKACR 574 H4E R172A* NGSALTNTWVDMTGARIAYKNWETEITAQPDGGFGVFGENCAVLSGAANGKWFDKRCA 575 [0374] *Note that the numbering of 056-53.H4E amino acids diverges from the TN
sequence numbering in the last four candidates listed, because of the introduction in loop 4 of three additional amino acids. Thus E153 in 056-53.H4E corresponds to E150 in the original TN
sequence (Figure 2, for example). Which figure does this go with?

RECTIFIED SHEET (RULE 91) ISA/EP

Affinity and production level in E.coli periplasm of 056-53.H4E ATRIMERTM
polypeptide complexes generated by alanine scanning Atrimer KD(nM) mg/L
056-53.H4E 0.772 1.430 H4E N I15A 7.560 0.923 H4E G I16A 10.700 1.680 WE S 117A 2.230 1.314 H4E LI19A 1.330 1.600 H4E TI20A 1.210 1.500 H4E N121 A 0.989 1.100 H4E T122A 6.690 1.000 H4E W 123A 11.500 1.100 H4E R 130A 1.570 1.940 H4E K134A 1.580 0.764 H4E N135A 1.170 0.546 WE W 136A 14.400 0.484 WE E 137A 0.597 1.850 H4E T138A 0.743 2.218 H4E E139A 0.640 1.194 WE I140A 1.280 1.706 H4E T141A 0.651 1.378 H4E Q143A 0.689 0.444 H4E D 145A 0.714 0.876 H4E G 146A 0.960 1.092 WE G 147A 1.030 0.512 H4E E153A* 0.948 0.750 H4E N 154A* 0.843 1.570 WE R170A* 0.777 1.984 H4E RI 72A* 1.080 0.836 [0375] Example 25 [0376] Subcloning and production of CTLD and ATRIMERTM polypeptide complex binders to human IL-23R

[0377] The DNA fragments encoding loop regions were obtained by restriction digestion with BglII and PstI (or Mfel) restriction enzymes, and ligated to the bacterial CTLD expression vectors pANAI (SEQ ID NO: 51), pANA3 (SEQ ID NO: 53), or pANAI2 (SEQ ID NO:
62) that RECTIFIED SHEET (RULE 91) ISA/EP

were pre-digested with Bg1II and PstI. pANA1 is a T7 based expression vector designed to express C-terminal 6xHis-tagged human monomeric CTLD. The pelB signal peptide directs the proteins to the periplasm or growth medium. pANA3 is the C-terminal HA-His-tagged version of pANAI. pANA12 is the C-terminal HA-Strepll-tagged version of pANAI. For expression of trimeric protein, the loop regions can be sub-cloned into ATRIMERTM
polypeptide complex expression vectors pANA4 (SEQ ID NO: 54) or pANA10 (SEQ ID NO: 60)to produce secreted ATRIMERTM polypeptide complexes in E. coli. pANA4 is a pBAD based expression vector containing C-terminal His/Myc-tagged full length human TN with an ompA signal peptide to direct the proteins to periplasm or growth medium. pANA10 is the C-terminal HA-Strepll-tagged version of pANA4.

[0378] The expression constructs were transformed into E. coli strains BL21(DE3). Star (for pANA 1, pANA3 and pANA 12; monomeric CTLD production) or BL21(DE3) (for pANA4 and pANA10; ATRIMERTM polypeptide copmlexproduction) were plated on LB/agar plates with appropriate antibiotics. A single colony on a fresh plate was inoculated into I L of either SB with 1% glucose and kanamycin (for pANAI and pANA12 vectors) or 2xYT (doubly concentrated yeast tryptone) medium with ampicillin (for pANA4 and pANA10 vectors). The cultures were incubated at 37 C on a shaker at 200 rpm to an OD600 of 0.5, then cooled to room temperature.
IPTG was added to a final concentration of 0.05 mM for pANAI and pANA12, while arabinosis was added to a final concentration of 0.002-0.02% for pANA4 and pANA10. The induction was performed overnight at room temperature with shaking at 120-150 rpm, after which the bacteria were collected by centrifugation. The periplasmic proteins were extracted by osmotic shock or gentle sonication.

[0379] The 6xHis-tagged proteins were purified using Ni+-NTA affinity chromatography.
Briefly, periplasmic proteins were reconstituted in a His-binding buffer (100 mM HEPES, pH
8.0, 500 mM NaCl, 10 mM imidazole) and loaded onto a Ni+-NTA column pre-equilibrated with His-binding buffer. The column was washed with I Ox volume of binding buffer.
The bound proteins were eluted with an elution buffer (100 mM HEPES, pH 8.0, 500 mM
NaCl, 500 mM
imidazole). The purified proteins were dialyzed into 1 X PBS buffer and bacterial endotoxin was removed by anion exchange.

RECTIFIED SHEET (RULE 91) ISA/EP

[0380] The strep II-tagged monomeric CTLDs and ATRIMERTM polypeptide complexes were purified by Strep-Tactin affinity chromatography. Briefly, periplasmic proteins were reconstituted in IX PBS buffer and loaded onto a Strep-Tactin column pre-equivalent with IX
PBS buffer. The column was washed with l OX volume of PBS buffer. The proteins were eluted with elution buffer (IX PBS with 2.5 mM desthiobiotin). The purified proteins were dialyzed into IX PBS buffer and bacterial endotoxin was removed by anion exchange.

[0381] For some cell assays, ATRIMERTM polypeptide complexes were produced by mammalian cells. DNA fragments encoding loop regions were sub-cloned into the mammalian expression vector pANA2 or pANAI I to produce ATRIMERTM polypeptide complexes in the HEK293 transient expression system. pANA2 is a modified pCEP4 vector containing a C-terminal His tag. pANAI I is the C-terminal HA-StrepII-tagged version of pANA2. The DNA
fragments encoding loop region were obtained by double digestion with Bgl1I
and MfeI and ligated into the expression vectors pANA2 and pANAI I pre-digested with BglII
and MfeI. The expression plasmids were purified from bacteria using a Qiagen HiSpeed Plasmid Maxi Kit (Qiagene). For HEK293 adhesion cells, transient transfection was performed using Qiagen SuperFect Reagent according to the manufacturer's protocol. The day after transfection, the medium was removed and changed to 293 Isopro serum-free medium (Irvine Scientific). Two days later, glucose in 0.5 M HEPES buffer was added into the media to a final concentration of I%. The tissue culture supernatant was collected 4-7 days after transfection for purification. For HEK 293F suspension cells, the transient transfection was performed by Invitrogen's 293Fectin according to the manufacturer's protocol. The next day, 1 X volume of fresh medium was added into the culture. The tissue culture supernatant was collected 4-7 days after transfection for purification.

[0382] The His or Strep II-tagged ATRIMERTM polypeptide complex purification from mammalian tissue culture supernatant was performed as described for E. coli produced ATRIMERTM polypeptide complexes.

[0383) Example 26 [0384] Characterization of binders by ELISA and competition ELISA

RECTIFIED SHEET (RULE 91) ISA/EP

[0385] ELISA assays, performed as described in Example 23, demonstrated that none of the phage-displayed binders cross-reacted with either human IgG I Fc or with recombinant mouse IL-23R/Fc (R&D Systems).

[0386] Competitive ELISA assays were performed using purified monomeric CTLDs or ATRIMERTM polypeptide complexes generated as described above from positive human IL-23R
(IL-23R) binders to block binding of human IL-23 to human IL-23R. Assays were performed generally as follows. Individual wells in Immulon HB2 plates were incubated overnight at 4 C
with 100 gL PBS containing 100 ng of an anti-human IgG Fc (R&D MAB 110 clone 97924).
Plates were washed five times with PBS/0.05% Tween 20, and wells were incubated for 1.5 h at RT with 100 L each of PBS containing 50 ng of recombinant human IL-23R/Fc.
Plates were washed as before and blocked for I h at RT with 150 pL of 3% bovine serum albumin (Sigma) in PBS, after which plates were washed as described, and wells were incubated for 1-2 hours at RT
with 100 L each of PBS containing IL-23 with or without competitor (ATRIMERTM
polypeptide copmlexor CTLD). IL-23-containing solutions were prepared as follows. Human IL-23 (eBioscience) was added at a concentration of 100 ng/mL. Competitor was included at a final concentration of I pg/mL. After incubation, plates were washed as described and wells were incubated for 40 min at RT with 100 L each of PBS containing a 1:5000 dilution of streptavidin-HRP conjugate (Pierce catalog no. 21130). After washing, wells were incubated with 100 L each of TMB (BioFX Lab catalog no. TMBH-1000-0) for up to 30 min at RT.
Reactions were stopped with an equal volume of 0.2 M sulfuric acid.

[0387] An example of the results of the competition assay (inhibiting IL-23/IL-23R interaction) using the ATRIMERTM polypeptide complexes from the initial panning is presented in Figure 11.
ATRIMERTM polypeptide complexes to the left of the wild-type human tetranectin control (TN) were obtained from the third round of panning against human IL-23R using the human Loop 1-4 library (except for P 1 D 1). ATRIMERTM polypeptide complexes to the right of the tetranectin control were obtained from the human 1-4 shuffle library after 3-4 rounds of panning on decreasing quantities of IL-23R. The ability of candidate molecules from the affinity-matured panning procedure to compete with IL-23 binding to IL-23R is improved over that of candidates from the initial panning procedure.

RECTIFIED SHEET (RULE 91) ISA/EP

[0388] A number of ATRIMERTM polypeptide complexes were tested in competition ELISA
more extensively to determine IC50 values. As shown in Table 19, ATRIMERTM
polypeptide complexes displayed low to subnanomolar IC50s.

Ability of ATRIMERTM polypeptide complexes to compete with IL-23 for binding to IL-23R.
hIL-23R binder SEQ ID NOS of Average IC50 Loops 1 & 4: (nM) H7H 378,389 0.53 H7B 440, 404 0.9 4G8 382,381 1.4 F7F 435,389 1.45 B5C 396, 389 1.65 A3C 434,389 1.8 056-53.H4E 396, 381 2.5 A9E 396, 395 2.6 H1G 436,381 3.75 The ATRIMERTM polypeptide complex 056-53.H4E was chosen as a standard for comparison, and additional competition assays were performed with affinity-matured ATRIMERTM
polypeptide complexes. Table 20 provides the ratio of the IC50 of tested ATRIMERTM
polypeptide complexes to that of 056-53.H4E performed in the same assay, in order to better compare competition results among assays.

Comparison of the ability of ATRIMERTM polypeptide complexes to compete with IL-23 for binding to IL-23R.

Ratio 1C50 to Ratio IC50 to 056- Ratio IC50 to 056-Atrimer 056-53.H4E 1C50 Atrimer 53.H4E IC50 Atrimer 53.H4E IC50 101-54-4136 0.3 105-08 2G10 1.8 101-51-1A8 3.7 105-08 1 D3 0.4 H4E N 154A 1.9 105-08 2G2 3.8 101-80-5E8 0.6 101-I I3-6C102 2.0 105-08 2H2 4.0 RECTIFIED SHEET (RULE 91) ISA/EP

H4E E137A 0.8 105-08 1C6 2.0 105-08 1C2 4.1 105-59-3B5 0.8 105-20IF3b 2.0 105-081B7 4.1 105-61-4G3 0.8 105-08 2H6 2.0 105-08 2D2 4.1 105-08 2C10 0.9 105-20 1 H7 2.1 105-20 2C4b 4.2 101-113-6C108 0.9 101-51-1A9 2.2 105-20 2F10 4.2 H4E T138A 1.0 105-08 2G1 2.2 105-08 1A10 4.3 105-78-2E6 1.0 105-08 2F6 2.4 105-08 1 D2 4.3 101-5l-1A7 1.0 105-08 I G9 2.4 105-08 21{l 1 4.3 101-51-IA4 1.0 105-201F3a 2.5 105-081D12 4.6 101-51- l A5 1.0 105-08 2G7 2.5 105-08 1 B 10 4.7 105-20 2G 12 1.0 105-08 2G4 2.5 105-20 2C 11 4.8 105-61-4G5 1.0 101-51-1 A6 2.6 105-08 100 5.0 101-54-4B3 1.0 105-08 l C U 2.8 105-08 2A 1 5.0 105-08 1 A3 1.1 105-20 2F 12 2.8 105-08 2H4 5.0 101-54-4AI2 1.1 105-20 2C4a 2.9 105-08 2G6 5.2 105-59-3A5 1.2 105-08 1 A7 2.9 105-08 2C9 5.3 H4E E 139A 1.2 105-08 2H3 2.9 105-20 2G5 5.3 105-20 2A3 1 . 2 105-08 2C4 2.9 105-08 I D I O 5.5 105-20 1 B3 1.2 105-20 1 B4 3.0 105-08 I G2 5.5 H4E D145A 1.3 105-08 1 B1 3.3 105-08 2H10 6.5 105-78-2D1 1.3 105-08 2C12 3.3 105-20 IA6 6.6 H4E T141 A 1.4 105-08 2H 12 3.3 105-08 1C9 7.4 101-54-4B 10 1.4 105-08 1 C4 3.3 105-08 2C8 8.4 WE R170A 1.4 105-08 2B3 3.4 101-51-IAIO 8.7 105-08 1A8 1.6 105-20 2C7 3.5 105-08 2C11 9.1 105-08 1 A4 1.6 105-08 1 DI 3.6 105-08 2E12 9.1 101-51-1 A3 1.6 105-08 2C 1 3.6 101-80-5H3 11.3 H4EQ143A 1.6 105-081C3 3.6 105-081G12 13.2 105-20 1 H 1 1.8 105-08 2C6 3.6 [0389] Example 27 [0390] Characterization of the affinity of human IL-23R binders by Biacore [0391 ] Apparent affinities of the monomeric and trimeric binders from both the original library panning and the affinity matured library pannings are provided in Tables 21, 22 and 23. A
Biacore 3000 biosensor (GE Healthcare) was used to evaluate the interaction of human IL-23R
and receptor binders. Immobilization of an anti-human IgG Fc antibody (GE
Heathcare) to the RECTIFIED SHEET (RULE 91) ISA/EP

CM5 chip (Biacore) was performed using standard amine coupling chemistry, and this modified surface was used to capture a recombinant human IL-23R/Fc fusion protein (R&D
Systems). A
low-density receptor surface, less than 200 RU, was used for all of the analyses. ATRIMERTM
polypeptide complex dilutions (1-500 nM) were injected over the IL-23R surface at 30 PUmin and kinetic constants were derived from the sensorgram data using the Biaevaluation software (version 3.1, GE Healthcare). Data collection was 3 minutes for the association and 5 minutes for dissociation. The anti-human IgG surface was regenerated with a 30s pulse of 3M
magnesium chloride. All sensorgrams were double-referenced against an activated and blocked flow-cell as well as buffer injections.

Affinities of monomeric CTLD IL-23R binders from H Loop 1-4 library Analyte K. (1/M-s) Kd (1/s) KA (1/M) Kp (nM) A5F 1.70E+05 4.15E-03 4.11E+07 24.3 4G8 1.43E+05 7.83E-03 1.83E+07 54 B1B 1.15E+05 6.46E-03 1.77E+07 56.4 A9E 3.81E+04 4.10E-03 9.29E+06 108 A8E 5.37E+04 7.57E-03 7.09E+06 141 4D4 2.83E+04 4.19E-03 6.76E+06 148 C7F 3.58E+04 5.31E-03 6.75E+06 148 C12E 4.16E+04 7.40E-03 5.62E+06 178 3C2 3.99E+04 7.41E-03 5.39E+06 186 C3C 8.45E+04 1.58E-02 5.34E+06 187 A4A 1.18E+05 2.29E-02 5.18E+06 193 4F5 2.35E+04 5.71 E-03 4.12E+06 243 B1A 2.18E+04 7.04E-03 3.09E+06 324 4E5 4.54E+04 1.61E-02 2.82E+06 355 B12C 1.26E+05 5.72E-02 2.20E+06 455 B7C 3.03E+04 1.99E-02 1.52E+06 656 RECTIFIED SHEET (RULE 91) ISA/EP

Affinities of full-length ATRIMERTM polypeptide complex IL-23R binders from the original and the first affinity-matured library."4G8 TN m" refers to mammalian-cell produced material. All other material was produced in E. coll.

Analyte K. (1/M-s) Kd (1/s) KA (11M) KD (nM) H7B 4.31E+05 2.40E-04 1.80E+09 0.557 B5C 3.07E+05 3.14E-04 9.78E+08 1.02 056-53.H4E 2.66E+05 3.14E-04 8.47E+08 1.18 F7F 2.98E+05 3.76E-04 7.92E+08 1.26 H7H 2.56E+05 3.85E-04 6.65E+08 1.5 A3C 2.13E+05 3.73E-04 5.70E+08 1.75 A9E 1.72E+05 3.30E-04 5.21E+08 1.92 B12F 2.44E+05 5.45E-04 4.47E+08 2.24 A5F 1.53E+05 7.00E-04 2.19E+08 4.57 4G8 m 1.58E+05 7.51 E-04 2.10E+08 4.76 MG 9.52E+04 4.89E-04 1.95E+08 5.13 B9B 9.28E+04 4.78E-04 1.94E+08 5.15 C7F 7.22E+04 4.65E-04 1.55E+08 6.44 4G8 1.09E+05 8.05E-04 1.35E+08 7.42 A4A 5.06E+04 4.09E-04 1.24E+08 8.08 C3C 5.79E+04 4.83E-04 1.20E+08 8.34 C6H 4.95E+04 8.45E-04 5.85E+07 17.1 Affinities of ATRIMERTM polypeptide complex IL-23R binders from additional affinity-matured libraries and alanine-scan candidates.
All material was produced in E. coli.

Analyte K. (1/M=s) Ka (1/s) KA (1/M) KD (nM) 101-113-6C102 2.71E+05 2.83E-04 9.62E+08 1.04 RECTIFIED SHEET (RULE 91) ISA/EP

101-113-6C108 6.23E+05 3.82E-04 1.63E+09 0.613 101-51-1 A I O 1.67E+05 3.45E-04 4.85E+08 2.06 101-51-1A3 4.63E+05 2.62E-04 1.77E+09 0.565 101-51-1A4 1.02E+06 3.95E-04 2.58E+09 0.388 101-51-1 A5 4.95E+05 2.89E-04 1.71E+09 0.584 101-51-1A6 5.57E+05 4.15E-04 1.34E+09 0.746 101-51-1 A7 4.19E+05 1.87E-04 2.24E+09 0.447 101-51-1 A8 2.62E+05 3.96E-04 6.62E+08 1.51 101-51-1A9 3.45E+05 3.29E-04 1.05E+09 0.955 101-54-4A 12 1.24E+06 5.73E-04 2.16E+09 0.463 101-54-4B 10 4.79E+05 4.29E-04 1.11E+09 0.897 101-54-4B3 1.13E+06 3.64E-04 3.12E+09 0.321 101-54-4B6 6.87E+05 3.90E-04 1.76E+09 0.569 101-80-5E8 1.13E+06 3.91E-04 2.89E+09 0.346 101-80-5H3 5.05E+04 3.27E-04 1.55E+08 6.46 105-081A3 7.35E+05 3.48E-04 2.11E+09 0.473 105-081A4 2.50E+05 3.12E-04 8.00E+08 1.250 105-08 I A8 7.37E+05 3.44E-04 2.14E+09 0.467 105-08 1 D3 2.28E+05 3.01 E-04 7.58E+08 1.320 105-08 2C 10 6.06E+05 3.71 E-04 1.63E+09 0.612 105-08 2F6 5.50E+05 3.59E-04 1.53E+09 0.653 105-08 2G10 3.02E+05 3.97E-04 7.58E+08 1.320 105-08 2G7 2.51E+05 3.58E-04 6.99E+08 1.430 105-20 1 B3 4.05E+05 3.10E-04 1.31E+09 0.764 105-201H1 3.74E+05 3.20E-04 1.17E+09 0.857 105-201H7 5.00E+05 3.72E-04 1.34E+09 0.744 105-20.2A3 4.12E+05 3.12E-04 1.32E+09 0.759 105-20 2F12 2.54E+05 4.71E-04 5.41E+08 1.850 105-20 2G 12 3.98E+05 2.62E-04 1.52E+09 0.658 H4E D145A 4.01 E+05 2.86E-04 1.40E+09 0.714 H4E E137A 4.37E+05 2.61E-04 1.68E+09 0.597 H4E E139A 4.19E+05 2.68E-04 1.56E+09 0.64 H4E N 154A 1.68E+05 1.42E-04 1.19E+09 0.843 RECTIFIED SHEET (RULE 91) ISA/EP

H4E Q143A 3.42E+05 2.36E-04 1.45E+09 0.689 H4E R170A 3.23E+05 2.51E-04 1.29E+09 0.777 H4ET138A 3.52E+05 2.61E-04 1.35E+09 0.743 H4E T141A 4.05E+05 2.64E-04 1.54E+09 0.651 H4EW 6.51E+05 3.64E-04 1.79E+09 0.560 [0392] Example 28 [0393] ATRIMERTM complexes binding to IL-23R do not recognize IL-12R(31 or IL-12R(32 [0394] A Biacore 3000 biosensor (GE Healthcare) was used to evaluate the interaction of human IL-12R(31/Fc or IL-12R(32/Fc with IL-23R binding ATRIMERTM complexes.
Immobilization of an anti-human IgG Fc antibody (GE Healthcare) to the CM5 chip (GE Healthcare) was performed using standard amine coupling chemistry, and this modified surface was used to capture recombinant human IL-12R(31/Fc or IL-12R(32/Fc fusion protein (R&D
Systems). A
low-density receptor surface, less than 200 RU, was used for all of the analyses. ATRIMERTM
complex dilutions (100 nM) were injected over the IL-12R surface at 30 d/min.
Data collection was 3 minutes for the association and 5 minutes for dissociation. The anti-human IgG surface was regenerated with a 30s pulse of 3M magnesium chloride. All sensorgrams were double-referenced against an anti-human IgG Fc antibody surface as well as buffer injections. As shown in Table 24, ATRIMERTM complexes did not show any measureable binding to human IL-12R[i1/Fc or IL-12R(32/Fc.

Table 24 ATRIMERTM
(100 nM) I112Rbl I112Rb2 105-08-1 A8 negative negative H4E-E 137A negative negative 101-54-4B6 negative negative 101-113-6C 108 negative negative 101-51-1 A4 negative negative RECTIFIED SHEET (RULE 91) ISA/EP

101-51-1 A7 negative negative 101-51- I A7F negative negative 105-08-1 A8 negative negative [0395] Example 29 [0396] Competitive assays of human IL-23 binding to IL-23R in the presence of IL-23R binders using Biacore [0397] IL-23R binding ATRIMERTM polypeptide complexes were amine-coupled to CM5 chips (GE Healthcare) then IL-23R (IL-23R) was injected over the chip surface.
Following binding stabilization, the ability of human IL-23 (eBioscience) to interact with IL-23R was monitored.
Additional competition assays were done by pre-forming a complex between IL-23R and IL-23 or IL-23R and ATRIMERTM polypeptide complexes for 30 minutes at room temperature. The complex was then injected over the surface with the amine-coupled ATRIMERTM
complexes.
Remaining binding of IL-23R Atrimer, as shown in Table 25 for Atrimer A5F was determined and expressed as percent of binding in the absence of competitor (IL-23 or different Atrimer).

Table 25 A5F competes with binding of IL-23 to the IL-23R
Anal to Percent binding to A517 rh1L23RFc 100 rhIL23RFc+rhIL23 19 rhIL23RFc+A9E 25 [0398] Example 30 [0399] Testing activity of selected ATRIMERTM polypeptide complex in cell based assay [0400] Human peripheral blood mononuclear cells (PBMC) from healthy donors (AllCells) were stimulated at 1x106 cells/mL with human recombinant IL-23 (1 ng/mL, eBioscience) and PHA (1 gg/mL, Sigma) in the presence of IL-23R ATRIMERTM polypeptide complexes or Ustekinumab in 10% FBS/Advanced RPMI media (Invitrogen). After 4 days in culture, cell supernatants were RECTIFIED SHEET (RULE 91) ISA/EP

collected and assayed by ELISA using IL- 17 Quantikine kits (R&D Systems). In parallel cultures, PBMC were treated with human recombinant IL-12 (1 ng/mL, R&D
Systems) in the presence of IL-23R ATRIMERTM polypeptide complexes or Ustekinumab for 4 days.
Cell supernatants were assayed for IFNy and IL- 17 by Luminex (Procarta, Panomics) and analyzed on the Bioplex system (BioRad). All treatments were performed in triplicate, and the mean and standard error were plotted using GraphPad Prism software. As shown in Figures 12, 13 and 14, IL-23 ATRIMERTM polypeptide complexes blocked IL-23-induced IL- 17 production, but did not inhibit IL-12-induced IFNy production. As expected, Ustekinumab inhibited both IL-23 and IL-12 responses.

[0401] Table 26 shows the results for affinity-matured ATRIMERTM polypeptide complexes tested in the PBMC assay. The ability of the ATRIMERTM polypeptide complexes to block IL-23-induced IL- 17, IL-I7F, and IL-22 production was measured for ATRIMERTM
polypeptide complexes as indicated. The results are shown as a ratio with the numerator being the IC50 for the ATRIMERTM polypeptide complexes compared to the IC50 for ustekinumab.
Results of more than one assay are shown for some ATRIMERTM polypeptide complexes.

Production levels of the indicated cytokines in the presence of each ATRIMERTM polypeptide complex compared to ustekinumab in the same experiment.
(Atrimer/Ustekinumab) ATRIMERTM
complex IL17 IL-17F IL22 101-113-6C108 0.013/1.03 0.41/0.77 105-08 I A8 0.14/0.16 0.42/0.1 0.2/1.03 4.9/1.05 101-51-1A4 0.12/0.47 0.09/0.25 0.27/0.09 0.1/0.47 0.18/0.25 8.8/0.56 5.2/0.55 101-54-4B6 0.15/0.16 0.11/0.1 0.12/0.09 2.1/0.34 H4E E137A 1.4/0.73 .16/0.55 101-51-1A7 1.8/0.58 4.4/0.44 101-54-4B3 3.6/0.16 0.16/0.1 105-08 2C10 3.1/0.47 5.2/0.25 1.8/0.09 101-54-4B10 4.4/0.93 6.6/2.3 101-80-5E8 7.9/1.03 12.9/0.77 RECTIFIED SHEET (RULE 91) ISA/EP

105-20 1117 16/0.33 4.2/0.43 114E T138A 8.8/0.73 13/0.34 056-53 H4E 17/0.73 45/0.34 101-51-1A5 34/0.58 18/0.44 105-08 I B7 19/0.93 225/2.3 105-08 ID3 109/0.58 31/0.44 105-20 2G12 158/0.93 601/2.3 105-081A3 233/3.0 201/3.3 [0402] Example 31 [0403] NKL Agonist Assay [0404] To show the lack of agonist activity of IL-23R ATRIMERTM polypeptide complexes on IL-23R, STAT-3 phosphorylation upon binding of selected IL-23R ATRIMERTM
complexes to the natural killer cell line NKL expressing the heterodimeric IL-23 receptor was determined.
ATRIMERTM complexes at a concentration of 150 ug/mL or IL-23 at 50 ng/mL as positive control were incubated at 37C with 140,000 NKL cells/well in a 96 well plate.
After 10 min, cells were centrifuged at 1200 rpm for 5 min, and washed with PBS twice. Then, cells were lysed and treated according to the protocol provided in the Stat3 phosphorylation kit that was obtained from Cell signaling technology (PATH SCAN Phospho Stat3 Sandwich ELISA kit, Cat #7300, Cell Signalling Technlogy, Inc., Danvers, Massachusettes). Stat-3 phopshorylation was measurd by adsorbance at 450 nM using a Molecular Devices ELISA reader. As shown in Figure 15 exemplary for complexes of H4E and H4EPI E9, no activation IL-23R
receptor by the complexes was observed, while IL-23 resulted in STAT-3 phosphorylation as expected. Similar results were obtained for all other atrimers tested such as 101 -51 -1 A4, 101-51-1 A7, 105-08-1 A8, 101-54-4B6, H4E E 137A, 101-113-6C 108 and 101-54-4B 10 as summarized in FIG. 16A
and 16B

[0405] Example 32 [0406] Panning of mouse 1-4 library on mouse IL-23R and identification of a mouse IL-23R-specific CTLD binder.

[0407] Panning & Screening of mouse library 1-4 RECTIFIED SHEET (RULE 91) ISA/EP

[0408] Phage generated from mouse library 1-4 were panned on recombinant mouse IL-23R/Fc chimera (R&D Systems). Screening of these binding panels using an ELISA plate assay after three rounds of panning identified a receptor-specific binder.

[0409] To generate phage for panning, the master library DNA was transformed by electroporation into bacterial strain ER2738 (Lucigen or NEB). Cells were allowed to recover for one hour with shaking at 37 C in SOC (Super-Optimal broth with Catabolite repression) medium prior to increasing the volume 10-fold by adding super broth (SB) to a final concentration of 20% glucose and 20 g/mL carbenicillin. After shaking at 37 C
for one hour, the carbenicillin concentration was increased to 50 g/mL for another hour, after which 400 mL
of SB with 2% glucose and 50 g/mL carbenicillin were added, along with helper phage M 13K07 to a final concentration of 5x 109 pfu/mL. Incubation was continued at 37 C without shaking for 30 minutes, and then with shaking at 100-150 rpm for another 30 min. Cells were centrifuged at 3200g at 4 C for 20 minutes, then resuspended in 500 mL SB
medium containing 50 g/mL carbenicillin and 50 g/mL kanamycin. Cells were grown overnight at room temperature (RT) with shaking at 150 rpm. Phage were isolated by pelleting the bacterial cells by centrifugation at 15,000 g and 4 C for 20 min. The supernatant was incubated with one-fourth volume (usually 250 mL of supernatant/bottle + 62.5 mL PEG solution) of 20%
PEG/2.5 M
NaCl on ice for 30 min. The phage was pelleted by centrifugation at 15,000 g and 4 C for 20 min. The phage pellet was resuspended in Buffer D, containing 0.05% boiled cassein, 0.025%
Tween-20, and protease inhibitors. Material was filter-sterilized using Whatman Puradisc 25 mm diameter, 0.2 gm pore size filters.

[0410] Phage generated from mouse library 1-4 were panned on recombinant mouse IL-23R/Fc chimera (R&D Systems cat #1686-MR) using a plate format. Six wells of a 96-well Immulon HB2 ELISA plate were coated with 250 -1000 ng/well of carrier-free mouse IL-23R/Fc in Dulbecco's PBS. Material was incubated on the plate overnight, after which wells were washed three times with PBS and blocking buffer ((Buffer C, containing 0.05% boiled casseing and I%
Tween-20) was added. Wells were incubated for at least 1 hour at 37 C.
Additional wells were also treated with blocking buffer at the same time for later absorption of phage binding to blocking buffer.

RECTIFIED SHEET (RULE 91) ISA/EP

[0411] Three dilutions of the phage preparation were used: undiluted, 1:10, and 1:100 in buffer D plus protease inhibitors. In the 3 round of panning, recombinant human IgGI
Fc was added to each of the dilutions to a final concentration of 10 gg/mL. Blocking buffer was removed from the "Block Only" (preabsorption to block) wells and the different phage mixtures were incubated in these wells for another hour at 37 C. Aliquots (50 L) of each phage mixture were transferred to a washed and blocked target well and allowed to incubate for 2 h at 37 C.
For the first round of panning, bound phage were washed once with Buffer D, and were eluted using glycine buffer, pH 2.2, containing I mg/mL BSA. After neutralization with 2 M Tris base (pH
11.5) the eluted phage were incubated for 15 minutes at room temperature with two to four milliliters of ER2738 cells (Lucigen or NEB) at an optical density of approximately 0.9 measured at 600 nm (OD600) in yeast extract-tryptone (YT) medium. Phage were prepared from this infection using the protocol above, but scaled down by about 20% (volume). Phage prepared from eluted phage were subjected to additional rounds of panning. At each round, titers of input and output phage were determined by plating on agar with appropriate antibiotics, and colonies from these plates were used later for screening for binders by ELISA.

[0412] Additional rounds of panning were performed as described above, except that in the second round of panning, washes were increased to 5x, and in subsequent rounds, washes were increased to 10x. Three to six rounds of panning were performed. For the final round of panning, phage were not produced after infection; rather, infected bacteria were grown overnight and a maxiprep (Qiagen kit) was prepared from the DNA. Glycerol stocks (15%) of input phage were stored frozen (at -80 C) from each round.

[0413] For ELISA screening, colonies from later rounds of panning were grown in YT medium with 2% glucose and antibiotics overnight, and an aliquot of each was then used to start fresh cultures that were grown to an OD600 of 0.5. Helper phage were added to 5 x 109 pfu/mL and allowed to infect for 30 min at 37 C, followed by growth at 37 C with agitation. Bacteria were centrifuged and resuspended in YT medium with carbenicillin and kanamycin and grown overnight for phage production. Bacteria were then pelleted and the medium was removed and mixed with one-fifth volume (1:5 milk mixture: supernatant) of 6X PBS, 18%
milk. ELISA plates were prepared by incubating overnight at 4 C with 50-100 L of PBS containing 75-100 ng/well of recombinant mouse IL-23R/Fc. A duplicate plate coated with human IgG Fc (R&D Systems) RECTIFIED SHEET (RULE 91) ISA/EP

was used as a control. Plates were washed 3 times with PBS, blocked for 1 h at 37 C with 3%
milk in 1 X PBS, and incubated for 1 hour with 100 uL/well of each milk-treated phage mixture.
Plates were washed once with PBS/0.05% Tween 20 and twice with PBS, incubated for one hour with an HRP-conjugated anti-M 13 antibody (GE Healthcare), washed three times each with PBS/Tween and PBS, and incubated with TMB substrate (VWR). Sulfuric acid was added to stop the color reaction and absorbance was read at 450 nm to identify positive binders.

[04141 A phage-displayed mouse TN CTLD that bound well to mouse IL-23R was identified from the third round of panning. The sequence from the randomized regions of Loops I and 4 from this binder is given in Table 27.

Table 27 Clone name Loo 1 SEQ ID NO Loo p4 SEQ ID NO

[0415] The above examples do not limit the scope of variation that can be generated in these libraries. Other libraries can be generated in which varying numbers of random or more targeted amino acids are used to replace existing amino acids, and different combinations of loops can be utilized. In addition, other mutations and methods of generating mutations, such as random PCR
mutagenesis, can be utilized to provide diverse libraries that can be subjected to panning.

[0416] Although various specific embodiments of the present invention have been described herein, it is to be understood that the invention is not limited to those precise embodiments and that various changes or modifications can be affected therein by one skilled in the art without departing from the scope and spirit of the invention.

[0417] The examples given above are merely illustrative and are not meant to be an exhaustive list of all possible embodiments, applications or modifications of the invention. Thus, various modifications and variations of the described methods and systems of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention.
Although the invention has been described in connection with specific embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the RECTIFIED SHEET (RULE 91) ISA/EP

invention which are obvious to those skilled in molecular biology, immunology, chemistry, biochemistry or in the relevant fields are intended to be within the scope of the appended claims.
[0418] It is understood that the invention is not limited to the particular methodology, protocols, and reagents, etc., described herein, as these may vary as the skilled artisan will recognize. It is also to be understood that the terminology used herein is used for the purpose of describing particular embodiments only, and is not intended to limit the scope of the invention.

[0419] The embodiments of the invention and the various features and advantageous details thereof are explained more fully with reference to the non-limiting embodiments and/or illustrated in the accompanying drawings and detailed in the following description. It should be noted that the features illustrated in the drawings are not necessarily drawn to scale, and features of one embodiment may be employed with other embodiments as the skilled artisan would recognize, even if not explicitly stated herein.

[0420] Any numerical values recited herein include all values from the lower value to the upper value in increments of one unit provided that there is a separation of at least two units between any lower value and any higher value. As an example, if it is stated that the concentration of a component or value of a process variable such as, for example, size, angle size, pressure, time and the like, is, for example, from I to 90, specifically from 20 to 80, more specifically from 30 to 70, it is intended that values such as 15 to 85, 22 to 68, 43 to 51, 30 to 32, etc. are expressly enumerated in this specification. For values which are less than one, one unit is considered to be 0.0001, 0.001, 0.01 or 0.1 as appropriate. These are only examples of what is specifically intended and all possible combinations of numerical values between the lowest value and the highest value enumerated are to be considered to be expressly stated in this application in a similar manner.

[04211 The disclosures of all references and publications cited herein are expressly incorporated by reference in their entireties to the same extent as if each were incorporated by reference individually.

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Claims

1. A combinatorial polypeptide library comprising polypeptide members that comprise a C-type lectin domain (CTLD) having a randomized loop region, wherein the CTLD loop region comprises loop segment A (LSA) containing Loops 1-4 and loop segment B (LSB) containing Loop 5 and is randomized according to one of the following Schemes:
(a) amino acid modifications in at least one of the four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise an insertion of at least one amino acid in Loop 1 and random substitution of at least five amino acids within Loop 1;
(b) amino acid modifications in at least one of the four loops in loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise random substitution of at least five amino acids within Loop 1 and random substitution of at least three amino acids within Loop 2;

(c) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise random substitution of at least seven amino acids within Loop 1 and at least one amino acid insertion in Loop 4;

(d) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise at least one amino acid insertion in Loop 3 and random substitution of at least three amino acids within Loop 3;

(e) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise a modification that combines two loops into a single loop, wherein the two combined loops are Loop 3 and Loop 4;

(f) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise at least one amino acid insertion in Loop 4 and random substitution of at least three amino acids within Loop 4;

(g) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD and in loop segment B (LSB), wherein the amino acid modifications comprise random substitution of at least five amino acid residues in Loop 3 and random substitution of at least three amino acids within Loop 5;

(h) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise random substitution of at least one amino acid and insertion of at least six amino acids in Loop 3;

(i) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise a mixture of (1) random substitution of at least six amino acids in Loop 3 and (2) random substitution of at least six amino acids and at least one amino acid insertion in Loop 3; and (j) amino acid modifications in at least one of the four loops in the loop segment A
(LSA) of the CTLD, wherein the amino acid modifications comprise at least four or more amino acid insertions in at least one of the four loops in the loop segment A
(LSA) or loop 5 in loop segment B (LSB) of the CTLD.

2. The library of claim 1, wherein the CTLD comprises the following secondary structure:
(a) five .beta.-strands and two .alpha.-helices sequentially appearing in the order .beta.1, .alpha.1, .alpha.2, .beta.2, .beta.3, .beta.4, and .beta.5, the .beta.-strands being arranged in two anti-parallel .beta.-sheets, one composed of .beta.1 and .beta.5, the other composed of .beta.2, .beta.3 and .beta.4;

(b) at least two disulfide bridges, one connecting .alpha.1 and .beta.5 and one connecting .beta.3 and the polypeptide segment connecting .beta.4 and .beta.5; and (c) a loop segment A (LSA) and a loop segment B (LSB), wherein LSA connects .beta.2 and .beta.3, and LSB connects .beta.3 and .beta.4.

3. The library of claim 1, further comprising random substitution of the amino acid located adjacent to the C-terminal end of Loop 2 in the C-terminal direction.

4. The combinatorial library of claim 1, wherein the CTLD is from human tetranectin and further comprises random substitution of Arginine-130.

5. The combinatorial library of claim 1, wherein the CTLD is from human or mouse tetranectin and further comprises a substitution of Lysine-148 to Alanine.

6. The combinatorial library of claim 4 having the randomized CTLD of Scheme (a), wherein the amino acid modifications comprise two amino acid insertions in Loop 1, random substitution of at least five amino acids within Loop 1, and a substitution of Lysine- 148 to Alanine.

7. The combinatorial library of claim 1 having the randomized CTLD of Scheme (c), wherein the amino acid modifications further comprise random substitution of at least two amino acids within Loop 4.

8. The combinatorial library of claim 7, wherein the amino acid modifications comprise random substitution of at least seven amino acids within Loop 1, at least three amino acid insertions in Loop 4, and random substitution of at least two amino acids within Loop 4.

9. The combinatorial library of claim 1 having the randomized CTLD of Scheme (d), wherein the amino acid modifications further comprise at least one amino acid insertion in Loop 4.

10. The combinatorial library of claim 9, wherein the amino acid modifications further comprise random substitution of at least three amino acids within Loop 4.

11. The combinatorial library of claim 10, wherein the amino acid modifications comprise three amino acid insertions in Loop 3.

12. The combinatorial library of claim 11, wherein the amino acid modifications comprise three amino acid insertions in Loop 4.

13. The combinatorial library of claim 1 having the randomized CTLD of Scheme (e), wherein the amino acid modifications comprise random substitution of at least six amino acids in Loop 3 and random substitution of at least four amino acids in Loop 4.

14. The combinatorial library of claim 13, wherein the CTLD is human or mouse tetranectin and wherein the amino acid modifications further comprise random substitution of Proline-144.

15. The combinatorial library of claim 14, wherein the combined Loop 3 and Loop 4 amino acid sequence comprises NWEXXXXXXX XGGXXXN (SEQ ID NO: 578), wherein X is any amino acid and wherein the amino acid sequence of SEQ ID NO: 578 forms a single Loop region.

16. The combinatorial library of claim 1 having the randomized CTLD of Scheme (f), wherein the amino acid modifications comprise four amino acid insertions in Loop 4 and random substitution of at least three amino acids within Loop 4.

17. The combinatorial library of claim 1 having the randomized CTLD of Scheme (g), further comprising one or more amino acid modifications in the Loop 4 region that modulates plasminogen-binding affinity of the CTLD.

18. The combinatorial library of claim 17, wherein the CTLD is from human or mouse tetranectin and the modification to Loop 4 comprises substitution of Lysine 148 to Alanine.

19. The combinatorial library of claim 1 having the randomized CTLD of Scheme (h), wherein the CTLD is from human or mouse tetranectin and wherein the amino acid modifications comprise random substitution of Isoleucine 140.

20. The combinatorial library of claim 19, further comprising one or more amino acid modifications in the Loop 4 region that modulates plasminogen-binding affinity of the CTLD.

21. The combinatorial library of claim 20, wherein the modification to Loop 4 comprises substitution of Lysine 148 to Alanine.

22. The combinatorial library of claim 1 having the randomized CTLD of Scheme (i), wherein the amino acid modifications comprise amino acid modifications in at least one of the four loops in the loop segment A (LSA) of the CTLD, wherein the amino acid modifications comprise a mixture of (1) random substitution of at least six amino acids in Loop 3; (2) random substitution of at least six amino acids and at least one amino acid insertion in Loop 3; and (3) random substitution of at least six amino acids and at least two amino acid insertions in Loop 3;

23. The combinatorial polypeptide library of claim 2, wherein the CTLD
comprises one or more amino acid modifications in any combination of two, three, four, or five of the loops in loop segment A (LSA) and loop segment B (LSB).

24. The combinatorial library of claim 1, wherein the amino acid modifications comprise modifications to CTLD amino acids outside of the LSA and LSB.

25. The combinatorial library of claim 1 wherein the CTLD is that of human tetranectin.

26. The combinatorial library of claim 1 wherein the CTLD is that of murine tetranectin.

27. The combinatorial library of claim 1, wherein the polypeptide members further comprise at least one of an N-terminal extension and a C-terminal extension of the CTLD.

28. The combinatorial library of claim 27, wherein the at least one of the N-terminal extension and C-terminal extension comprises polypeptides providing effector function, enzyme function, further binding function, or multimerizing function.

29. The combinatorial library of claim 27, wherein the at least one of the N-terminal extension and the C-terminal extension comprises the non-CTLD-portions of a native C-type lectin-like protein or C-type lectin or a C-type lectin lacking a functional transmembrane domain.

30. The combinatorial library of claim 29, wherein the proteins are multimers of a moiety comprising the CTLD.

31. A library of nucleic acid molecules encoding polypeptides of the combinatorial polypeptide library of claim 1.

32. The library of nucleic acid molecules of claim 31, wherein the nucleic acids molecules of the library are expressed in a display system, wherein the display system comprises an observable phenotype that represents at least one property of the displayed expression products and the corresponding genotypes.

33. A display system comprising the library of nucleic acid molecules of claim 31, wherein the display system is selected from a phage display system; a yeast display system; a viral display system; a cell-based display system; a ribosome-linked display system;
and a plasmid-linked display system.

34. A method for generating the combinatorial library of claim 1 comprising creating any of Schemes (a)-(j) by generating at least one random mutation in at least one of the four loops in the LSA region of the CTLD.

35. The method of claim 34, wherein the at least one random mutation is created by oligonucleotide-directed randomization; DNA shuffling by random fragmentation;
loop shuffling; loop walking; or error-prone PCR mutagenesis.

36. A method for identifying and isolating a polypeptide having specific binding activity to a target molecule, wherein the method comprises:
(a) providing a combinatorial polypeptide library of claim 1;
(b) contacting the combinatorial polypeptide library with the target molecule under conditions that allow for binding between a polypeptide and the target molecule;
and (c) isolating a polypeptide that binds to the target molecule.

37. The method of claim 36, wherein the method further comprises a library of nucleic acid molecules encoding polypeptides of the combinatorial polypeptide library, wherein the library of nucleic acids is expressed in a display system, and wherein the display system comprises an observable phenotype that represents at least one property of the displayed expression products and the corresponding genotypes.

38. A method for the identification and isolation of a polypeptide capable of specifically binding to a target molecule, said method comprising the steps of:
(a) providing a library of nucleic acid molecules encoding the polypeptide library of claim 1;
(b) expressing the library of nucleic acid molecules in a display system to obtain an ensemble of polypeptides, in which the amino acid residues at one or more sequence positions differ between different members of said ensemble of polypeptides;
(c) contacting the ensemble of polypeptides with said target molecule under conditions that allow for binding between a polypeptide and the target molecule;
and (d) isolating a polypeptide that is capable of binding to said target molecule.

39. A polypeptide having the scaffold structure of a C-type Lectin Like Domain (CTLD), wherein the polypeptide binds to a target other than a natural target for that CTLD, and wherein the CTLD scaffold structure of the CTLD is modified according to any of the schemes of claim 1.

40. The polypeptide of claim 39, wherein the polypeptide has the scaffold structure of the C-type Lectin Like Domain (CTLD) of human tetranectin and wherein the polypeptide binds to a target other than a natural target for human tetranectin.

41. A method for producing the polypeptide of claim 39, comprising contacting the combinatorial polypeptide library of claim 1 with the target molecule under conditions that allow for binding between the polypeptide and the target molecule and isolating a polypeptide that binds to the target molecule, wherein the target molecule is not the natural target for the CTLD.