通过XIAP抑制caspase-3的结构基础
S J Riedl1, M Renatus, R Schwarzenbacher
1The Program in Apoptosis and Cell, Death Research, The Burnham Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA.
Cell
|March 21, 2001
概括
与X链接的亡蛋白抑制剂 (XIAP) 通过独特的固体阻断机制阻断caspase-3活性. 这种结构性洞察力揭示了XIAP如何使用XIAP.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 结构生物学 结构生物学
背景情况:
- 通过卡斯巴酶抑制来调节亡并未完全被理解.
- 亡蛋白抑制剂 (IAP) 家族成员,如XIAP,是关键的内源性酶抑制剂.
- XIAP的目标是启动者caspase-9和执行者caspase-3和-7.
研究的目的:
- 阐明XIAP对卡斯巴酶抑制的分子机制.
- 确定XIAP的BIR2域与-3复合体中的晶体结构.
主要方法:
- 使用X射线结晶学来确定结构.
- 该结构的分辨率为2.7A分辨率.
主要成果:
- 获得了与酶-3结合的XIAP BIR2域的晶体结构.
- XIAP通过其BIR域的有限接触和其N终端扩展的广泛接触与caspase-3相互作用.
- N-终端延伸以反向的方向占据基板结合裂,导致硬质障碍.
结论:
- 结构数据显示,XIAP通过固体阻断抑制酶-3,防止基质结合.
- 这种机制与合成基质模拟抑制剂的机制不同.
- 了解XIAP的抑制机制提供了对亡调节的见解.
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