INHIBITION OF ALZHEIMER BETA-PEPTIDE FIBRIL FORMATION BY SERUM AMYLOID-P COMPONENT

被引:72
作者
JANCIAUSKIENE, S
DE FRUTOS, PG
CARLEMALM, E
DAHLBACK, B
ERIKSSON, S
机构
[1] UNIV LUND HOSP, ELECTRONMICROSCOPY UNIT, S-22185 LUND, SWEDEN
[2] UNIV LUND HOSP, DEPT MED, S-22185 LUND, SWEDEN
[3] UNIV LUND HOSP, DEPT CLIN CHEM, S-22185 LUND, SWEDEN
关键词
D O I
10.1074/jbc.270.44.26041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A 39-43-amino acid residue-long fragment (beta-peptide) from the amyloid precursor protein is the predominant component of amyloid deposits in the brain of individuals with Alzheimer's disease, Serum amyloid P component (SAP) is present in all types of amyloid, including that of Alzheimer's disease, We have used an in vitro model to study the effects of purified SAP on the fibril formation of synthetic Alzheimer beta-peptide 1-42, SAP was found to inhibit fibril formation and to increase the solubility of the peptide in a dose-dependent manner, At a 5:1 molar ratio of A beta 1-42 peptide to SAP, fibril formation was completely inhibited, and approximately 80% of the peptide remained in solution even after 4 days of incubation, At lower SAP concentrations, e,g, at peptide to SAP ratio of 1000:1, short fibrillar like structures, lacking amyloid characteristics, were formed, These structures frequently contained associated SAP molecules, suggesting that SAP binds to the polymerizing peptide in a reaction which prevented further fibril formation.
引用
收藏
页码:26041 / 26044
页数:4
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