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Genes & Development          doi: 10.1101/gad.224428.113
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Mechanistic insights into CED-4-mediated activation of CED-3

Weijiao Huang1£¬2£¬ Tianyu Jiang1£¬2£¬ Wooyoung Choi1£¬2£¬ Shiqian Qi1£¬2£¬ Yuxuan Pang1£¬2£¬ Qi Hu1£¬2£¬ Yanhui Xu3£¬ Xinqi Gong1£¬2£¬ Philip D. Jeffrey4£¬ Jiawei Wang5 and Yigong Shi1£¬2£¬6

Programmed cell death in Caenorhabditis elegans requires activation of the caspase CED-3£¬ which strictly depends on CED-4. CED-4 forms an octameric apoptosome£¬ which binds the CED-3 zymogen and facilitates its autocatalytic maturation. Despite recent advances£¬ major questions remain unanswered. Importantly£¬ how CED-4 recognizes CED-3 and how such binding facilitates CED-3 activation remain completely unknown. Here we demonstrate that the L2¡ä loop of CED-3 directly binds CED-4 and plays a major role in the formation of an active CED-4¨CCED-3 holoenzyme. The crystal structure of the CED-4 apoptosome bound to the L2¡ä loop fragment of CED-3£¬ determined at 3.2 £¿ resolution£¬ reveals specific interactions between a stretch of five hydrophobic amino acids from CED-3 and a shallow surface pocket within the hutch of the funnel-shaped CED-4 apoptosome. Structure-guided biochemical analysis confirms the functional importance of the observed CED-4¨CCED-3 interface. Structural analysis together with published evidence strongly suggest a working model in which two molecules of CED-3 zymogen£¬ through specific recognition£¬ are forced into the hutch of the CED-4 apoptosome£¬ consequently undergoing dimerization and autocatalytic maturation. The mechanism of CED-3 activation represents a major revision of the prevailing model for initiator caspase activation.

[ Last edited by ¹þ¹þ´ó¹ÃÒ¯ on 2013-10-20 at 09:06 ]
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