Inhibition of Alzheimer's amyloidosis by peptides that prevent beta-sheet conformation

被引:422
作者
Soto, C
Kindy, MS
Baumann, M
Frangione, B
机构
[1] NYU,MED CTR,DEPT PATHOL,NEW YORK,NY 10016
[2] UNIV KENTUCKY,DEPT BIOCHEM,LEXINGTON,KY 40536
关键词
D O I
10.1006/bbrc.1996.1413
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
Amyloid beta-peptide (A beta) is a major fibrillar component of neuritic plaques in Alzheimer's disease (AD) brains and is related to the pathogenesis of the disease. We hypothesized that amyloid formation could be inhibited by peptides homologous to A beta (position 17-21) with a similar degree of hydrophobicity, but with a very low propensity to adopt a beta-sheet conformation by incorporating proline residues (anti-beta-sheet peptides or beta-sheet inhibitors). An 11-residue peptide with these characteristics binds to A beta, inhibits A beta fibril formation and partially disaggregates preformed fibrils in vitro. Shorter anti-beta-sheet peptides and analogs containing D-amino acids are also able to inhibit A beta fibrillogenesis. The latter are more resistant to proteolytic degradation and may serve as a starting point to design more efficient peptides derivatives to inhibit amyloidogenesis in vivo. (C) 1996 Academic Press, Inc.
引用
收藏
页码:672 / 680
页数:9
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