识别和抑制哺乳动物亡所必需的ICE/CED-3蛋白酶
D W Nicholson1, A Ali, N A Thornberry
1Department of Biochemistry and Molecular Biology, Merck Frosst Centre for Therapeutic Research, Pointe Claire-Dorval, Quebec, Canada.
Nature
|July 6, 1995
概括
研究人员净化了apopain (也称为CPP32),这是一种对细胞亡 (编程细胞死亡) 至关重要的蛋白酶. 一种抑制剂阻止了细胞死亡,证实了apopain/CPP32的存在.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 细胞亡,或编程细胞死亡,是一个重要的细胞过程.
- 已知特定的蛋白酶参与了亡的执行.
- 确切的分子机制启动亡需要进一步阐明.
研究的目的:
- 为了净化和表征蛋白质酶,负责在亡过程中聚聚 (ADP-ribose) 聚合酶裂变.
- 为了确定参与启动细胞死亡的酶.
- 开发和测试这种蛋白酶的抑制剂.
主要方法:
- 使用酶净化技术来分离蛋白酶.
- 进行了酶子单元和前酶的表征.
- 试验室试验用于测试类化抑制剂的疗效.
主要成果:
- 这种名为apopain (CPP32) 的蛋白酶经过净化,发现它由来自CPP32前酶的17K和12K子单元组成.
- CPP32与中白素-1β转化酶 (ICE) 和Caenorhabditis elegans CED-3具有同源性.
- 一种类甲抑制剂在体外有效地阻止了apoptotic事件.
结论:
- 阿波/CPP32是apoptotic通路中的一个关键蛋白酶.
- 这种酶在启动编程细胞死亡方面发挥着至关重要的作用.
- 用抑制剂向阿波/CPP32是一种潜在的治疗策略,用于控制亡.
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