Nicholson D W, Ali A, Thornberry N A, Vaillancourt J P, Ding C K, Gallant M, Gareau Y, Griffin P R, Labelle M, Lazebnik Y A
Department of Biochemistry and Molecular Biology, Merck Frosst Centre for Therapeutic Research, Pointe Claire-Dorval, Quebec, Canada.
Nature. 1995 Jul 6;376(6535):37-43. doi: 10.1038/376037a0.
The protease responsible for the cleavage of poly(ADP-ribose) polymerase and necessary for apoptosis has been purified and characterized. This enzyme, named apopain, is composed of two subunits of relative molecular mass (M(r)) 17K and 12K that are derived from a common proenzyme identified as CPP32. This proenzyme is related to interleukin-1 beta-converting enzyme (ICE) and CED-3, the product of a gene required for programmed cell death in Caenorhabditis elegans. A potent peptide aldehyde inhibitor has been developed and shown to prevent apoptotic events in vitro, suggesting that apopain/CPP32 is important for the initiation of apoptotic cell death.
负责切割聚(ADP - 核糖)聚合酶且对细胞凋亡必不可少的蛋白酶已被纯化和鉴定。这种酶名为凋亡蛋白酶,由相对分子质量(M(r))为17K和12K的两个亚基组成,它们源自一种被鉴定为CPP32的共同前体酶。这种前体酶与白细胞介素 - 1β转换酶(ICE)和秀丽隐杆线虫程序性细胞死亡所需基因的产物CED - 3相关。一种有效的肽醛抑制剂已被开发出来,并显示出能在体外阻止凋亡事件,这表明凋亡蛋白酶/CPP32对凋亡性细胞死亡的启动很重要。