通过DPP9抑制NLRP1的结构和生化机制
Menghang Huang1, Xiaoxiao Zhang1, Gee Ann Toh2
1Beijing Advanced Innovation Center for Structural Biology, Tsinghua-Peking Joint Center for Life Sciences, Center for Plant Biology, School of Life Sciences, Tsinghua University, Beijing, China.
Nature
|March 18, 2021
概括
DPP8和DPP9抑制NLRP1炎症酶的激活. 结构和生化研究显示DPP9与NLRP1形成复合体,通过自身抑制机制抑制其激活.
科学领域:
- 免疫学
- 分子生物学
- 结构生物学
背景情况:
- 核酸结合域,富含白素的重复受体 (NLR) 是通过炎症体形成的先天免疫的关键媒介.
- NLRP1炎症酶的激活取决于其功能寻找域 (FIIND) 内的自分裂.
- 已知DPP8和DPP9抑制NLRP1的激活,但其机制尚不清楚.
研究的目的:
- 阐明DPP9抑制NLRP1激活的机制.
- 研究NLRP1和DPP9之间相互作用的结构基础.
主要方法:
- 用X射线结晶学来确定NLRP1-DPP9复合物的结构.
- 生物化学测试以评估结合和酶活性.
- 在人体细胞中进行功能测试以评估NLRP1抑制.
主要成果:
- 发现了一种2:1的老鼠NLRP1 (rNLRP1) 和老鼠DPP9 (rDPP9) 复合物,其中含有自身抑制的rNLRP1和活跃的UPA- CARD片段.
- NLRP1 的 ZU5 域对自身抑制和复合组合至关重要.
- 对于抑制人类细胞中的NLRP1激活,DPP9结合和酶活性都是必要的.
结论:
- DPP9通过形成增强自身抑制的复合物来抑制NLRP1炎症酶的激活.
- 这项研究揭示了DPP9介导的NLRP1抑制的分子机制.
- 这些发现为NLRP1炎症酶激活提供了洞察力.
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