Fraser et al., 1992 - Google Patents
Fibril formation by primate, rodent, and Dutch-hemorrhagic analogs of Alzheimer amyloid. beta.-proteinFraser et al., 1992
- Document ID
- 7105918165452954922
- Author
- Fraser P
- Nguyen J
- Inouye H
- Surewicz W
- Selkoe D
- Podlisny M
- Kirschner D
- Publication year
- Publication venue
- Biochemistry
External Links
Snippet
Revised Manuscript Received August 10, 1992 abstract: Deposition of extraneuronal fibrils that assemble from the 39-43 residue 3/A4 amyloid protein is one of the earliest histopathological features of Alzheimer's disease. We have used negative-stain electron …
- 241000288906 Primates 0 title abstract description 23
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4711—Alzheimer's disease; Amyloid plaque core protein
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6893—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids related to diseases not provided for elsewhere
- G01N33/6896—Neurological disorders, e.g. Alzheimer's disease
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4713—Autoimmune diseases, e.g. Insulin-dependent diabetes mellitus, multiple sclerosis, rheumathoid arthritis, systemic lupus erythematosus; Autoantigens
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/1703—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- A61K38/1709—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/43504—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Fraser et al. | Fibril formation by primate, rodent, and Dutch-hemorrhagic analogs of Alzheimer amyloid. beta.-protein | |
US6462171B1 (en) | Peptides and pharmaceutical compositions thereof for treatment of disorders or diseases associated with abnormal protein folding into amyloid or amyloid-like deposits | |
Hatami et al. | Familial Alzheimer’s disease mutations within the amyloid precursor protein alter the aggregation and conformation of the amyloid-β peptide | |
Pike et al. | Structure‐activity analyses of β‐amyloid peptides: contributions of the β25–35 region to aggregation and neurotoxicity | |
Fraser et al. | α1‐Antichymotrypsin binding to Alzheimer Aβ peptides is sequence specific and induces fibril disaggregation in vitro | |
Fraser et al. | Conformation and fibrillogenesis of Alzheimer Aβ peptides with selected substitution of charged residues | |
GALBETE et al. | Cholesterol decreases secretion of the secreted form of amyloid precursor protein by interfering with glycosylation in the protein secretory pathway | |
WALSH et al. | In vitro studies of amyloid β-protein fibril assembly and toxicity provide clues to the aetiology of Flemish variant (Ala692→ Gly) Alzheimer's disease | |
Sian et al. | Oligomerization of β-amyloid of the Alzheimer’s and the Dutch-cerebral-haemorrhage types | |
Millucci et al. | Conformations and biological activities of amyloid beta peptide 25-35 | |
Salon et al. | Relationship between β-amyloid degradation and the 26S proteasome in neural cells | |
Burdick et al. | Assembly and aggregation properties of synthetic Alzheimer's A4/beta amyloid peptide analogs. | |
DE69621607T2 (en) | CONNECTIONS WITH AGGREGATION-MODULATING EFFECT ON THE AMYLOiD PROTEIN | |
Carter | The Interaction of Amyloid-β with ApoE: The form of beta amyloid is a partial determinant of the interaction with Apolipoprotein E | |
Hubin et al. | Two distinct β-sheet structures in Italian-mutant amyloid-beta fibrils: a potential link to different clinical phenotypes | |
Di Fede et al. | Good gene, bad gene: new APP variant may be both | |
Soto et al. | Amyloid inhibitors and β-sheet breakers | |
El‐Agnaf et al. | The influence of the central region containing residues 19− 25 on the aggregation properties and secondary structure of Alzheimer's β‐amyloid peptide | |
Galzitskaya | New mechanism of amyloid fibril formation | |
Bentley et al. | Apolipoprotein E structural requirements for the formation of SDS-stable complexes with β-amyloid-(1–40): the role of salt bridges | |
Matsunaga et al. | A pH-dependent conformational transition of Aβ peptide and physicochemical properties of the conformers in the glial cell | |
Matsunaga et al. | Conformational changes preceding amyloid-fibril formation of amyloid-beta and stefin B; parallels in pH dependence | |
Walsh et al. | The many faces of Aβ: structures and activity | |
Soreghan et al. | The influence of the carboxyl terminus of the Alzheimer Aβ peptide on its conformation, aggregation, and neurotoxic properties | |
Estrada et al. | Protein misfolding disorders and rational design of antimisfolding agents |