Structure and zymogen activation of caspases

被引:95
作者
Donepudi, M [1 ]
Grütter, MG [1 ]
机构
[1] Univ Zurich, Inst Biochem, CH-8057 Zurich, Switzerland
关键词
caspases; inhibitor binding; structure comparison; X-ray structure; apoptosis; zymogen activation;
D O I
10.1016/S0301-4622(02)00151-5
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
Apoptosis is primarily executed by active caspases, which are derived from the inactive zymogens. Structural and biochemical studies of caspases-1, -3, -7, -8 and -9 have greatly enhanced our understanding of the structure, function, and specificity of the active form of these enzymes. Only recently, the structures of procaspase-7 and biochemical studies of procaspase-9 and -8 have provided insight into the process of procaspase activation. The mechanism of zymogen activation requires limited proteolysis as for many other proteases. In addition, self-activation through oligomerization has been demonstrated for the initiator caspases-8, -9 and -10. These studies provide a structural mechanism for caspase activation, substrate/inhibitor binding, and contribute to the understanding of the biological role of caspases in the processes of apoptosis. (C) 2002 Elsevier Science B.V All rights reserved.
引用
收藏
页码:145 / 153
页数:9
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