Development of retro-inverso peptides as anti-aggregation drugs for β-amyloid in Alzheimer's disease

被引:41
|
作者
Matharu, Balpreet [1 ]
El-Agnaf, Omar [2 ]
Razvi, Amna [1 ]
Austen, Brian M. [1 ]
机构
[1] Univ London, Neurodegenerat Unit, London SW17 0RE, England
[2] United Arab Emirates Univ, Fac Med & Hlth Sci, Dept Biochem, Al Ain 17666, U Arab Emirates
关键词
beta-Amyloid; Alzheimer's disease; Aggregation; OLIGOMERIZATION; AGGREGATION; TOXICITY;
D O I
10.1016/j.peptides.2010.06.033
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
Alzheimer's disease (AD) is a devastating degenerative disorder of the brain for which there is no cure or effective treatment. There is much evidence to suggest that beta-amyloid protein (A beta) aggregation in the brain leading to deposits is an important step in the development of AD. Recently, two peptides, RGKLVFFGR (OR1) and RGKLVFFGR-NH2 (OR2) containing the sequence KLVFF, which is the central region (residues 16-20) of A beta, have been found to be potent inhibitors of A beta aggregate formation. Here we report that retro-inversion of these sequences increases efficacy of the peptides in the inhibition of aggregation and toxicity of beta-amyloid. We describe the synthesis and inhibitory properties of these retro-inverso peptides. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1866 / 1872
页数:7
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