双环E3架构通过APC/C调节多环化和环链延长
Nicholas G Brown1, Ryan VanderLinden2, Edmond R Watson1
1Department of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Cell
|June 4, 2016
概括
亚纳相促进复合体/循环体 (APC/C) 使用不同的E2酶架构来控制蛋白质无处不在. 特殊的结构使得多管化和链接特定的多管链延长成为可能.
科学领域:
- 分子生物学
- 生物化学
- 结构生物学
背景情况:
- 蛋白质无化是一种由E1,E2和E3酶调节的关键的翻译后修饰.
- E2 和 RING E3 连接酶与无基合作,导致多基化或多基链延长.
研究的目的:
- 阐明人类E3无相促进复合体/循环体 (APC/C) 和其E2合作伙伴UBE2C和UBE2S的专门催化结构.
- 定义APC/C-E2相互作用决定不同形式的多化.
主要方法:
- 低温电子显微镜 (cryo-EM) 用于确定高分辨率结构.
- 用于分析酶活性和基质相互作用的生物化学测试.
主要成果:
- APC/C RING通过将其定位在基板和基板连接的ubiquitin附近来限制UBE2C的过程性多重化.
- 在链延长过程中,APC/C RING通过库林相互作用定位UBE2S来捕获正在演变的基质链.
结论:
- 专门的E3-E2基板-泛素架构控制着不同的聚聚素化路径.
- 这些发现揭示了APC/C调节和多化控制的新机制.
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