Caspase substrates

被引:322
作者
Timmer, J. C.
Salvesen, G. S.
机构
[1] Burnham Inst Med Res, Program Apoplosis & Cell Death Res, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Grad Program Mol Pathol, La Jolla, CA 92037 USA
关键词
apoptosis; protease; synthetic substrate; substrate prediction;
D O I
10.1038/sj.cdd.4402059
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 relatively common occurrence of sequences within proteins that match the consensus substrate specificity of caspases in intracellular proteins suggests a multitude of substrates in vivo - somewhere in the order of several hundred in humans alone. Indeed, the list of proteins that are reported to be cleaved by caspases in vitro proliferates rapidly. However, only a few of these proteins have been rigorously established as biologically or pathologically relevant, bona fide substrates in vivo. Many of them probably simply represent 'innocent bystanders' or erroneous assignments. In this review we discuss concepts of caspase substrate recognition and specificity, give resources for the discovery and annotation of caspase substrates, and highlight some specific human or mouse proteins where there is strong evidence for biologic or pathologic relevance.
引用
收藏
页码:66 / 72
页数:7
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