Amyloid β-degrading cryptidases:: insulin degrading enzyme, presequence peptidase, and neprilysin

被引:141
作者
Malito, E. [1 ]
Hulse, R. E. [2 ]
Tang, W. -J. [1 ,2 ]
机构
[1] Univ Chicago, Ben May Dept Canc Res, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Neurobiol, Chicago, IL 60637 USA
关键词
Alzheimer's disease; amyloid-beta peptide; metalloprotease; anti-amyloidogenic therapy; X-ray crystallography; insulin-degrading enzyme; presequence peptidase; neprilysin;
D O I
10.1007/s00018-008-8112-4
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
The accumulation of aggregates of amyloidogenic peptides is associated with numerous human diseases. One well studied example is the association between deposition of amyloid beta (A beta) and Alzheimer's disease. Insulin degrading enzyme and neprilysin are involved in the clearance of A beta, and presequence peptidase is suggested to play a role in the degradation of mitochondrial A beta. Recent structural analyses reveal that these three peptidases contain a catalytic chamber (crypt) that selectively encapsulates and cleaves amyloidogenic peptides, hence the name cryptidase. The substrate selectivity of these cryptidases is determined by the size and charge distribution of their crypt as well as the conformational flexibility of substrates. The interaction of A beta with the catalytic core of these cryptidases is controlled by conformational changes that make the catalytic chambers accessible for A beta binding. These new structural and biochemical insights into cryptidases provide potential therapeutic strategies for the control of A beta clearance.
引用
收藏
页码:2574 / 2585
页数:12
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