激活GLP-1受体与G蛋白复合的冷EM结构
Yan Zhang1, Bingfa Sun2, Dan Feng2
1Life Sciences Institute and Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
Nature
|May 25, 2017
概括
葡萄糖类1 (GLP-1) 通过结合由细胞外环和跨膜核形成的口袋来激活其受体 (GLP-1R). 这种结构洞察力揭示了GLP-1R-Gs复合体的形成,进步了对B类GPCR激活的理解.
科学领域:
- 结构生物学
- 生物化学
- 分子药理学
背景情况:
- 葡萄糖类1 (GLP-1) 是一种调节葡萄糖平衡和食欲的关键激素.
- GLP-1通过激活GLP-1受体 (GLP-1R),一种B类G蛋白结合受体 (GPCR) 来发挥作用.
- 了解B类GPCR激活的机制至关重要,但由于缺乏激活的全长受体的结构数据而受到限制.
研究的目的:
- 确定激活GLP-1受体-G复合物的近原子分辨率冷电子显微镜结构.
- 阐明由激素激活B类GPCR的结构基础.
主要方法:
- 使用冷电子显微镜 (cryo-EM) 可视化GLP- 1R- G复合体.
- 对该复合体进行了近原子分辨率结构分析.
主要成果:
- 结构显示激素由受体的N-终端域,跨膜核心和细胞外环形成的结合口袋内保持.
- 激素结合会导致跨膜域的构造变化,特别是跨膜螺旋6的扭曲.
- 这种形状变化促进了螺旋6的细胞内半部分向外旋转,以适应Gs蛋白的α5螺旋.
结论:
- 这项研究为了解激素结合时B类GPCRs的激活机制提供了第一个结构框架.
- 这种结构洞察对于合理设计针对GLP-1R和相关受体的疗法至关重要.
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