Inhibition of protein aggregation and amyloid formation by small molecules

被引:257
作者
Doig, Andrew J. [1 ]
Derreumaux, Philippe [2 ,3 ]
机构
[1] Univ Manchester, Fac Life Sci, Manchester Inst Biotechnol, Manchester M1 7DN, Lancs, England
[2] Univ Paris Diderot, UPR CNRS 9080, Lab Biochim Theor, Sorbonne Paris Cite,IBPC, F-75005 Paris, France
[3] Inst Univ France, F-75005 Paris, France
关键词
ALZHEIMERS-DISEASE; EPSILON-VINIFERIN; BETA OLIGOMERS; TOXICITY; DESIGN; EGCG; MUTATION; BEHAVIOR; FIBRILS; COMPLEX;
D O I
10.1016/j.sbi.2014.12.004
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
For decades, drug after drug has failed to slow the progression of Alzheimer's disease in human trials. How compounds reducing fibril formation in vitro and toxicity in transgenic mice and flies bind to the A beta toxic oligomers, is unknown. This account reviews recent drugs mainly targeting A beta, how they were identified and report their successes from in vitro and in vivo experimental studies and their current status in clinical trials. We then focus on recent in vitro and simulation results on how inhibitors interact with A beta monomers and oligomers, highly desirable knowledge for predicting new efficient drugs. We conclude with a perspective on the future of the inhibition of amyloid formation by small molecules.
引用
收藏
页码:50 / 56
页数:7
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