GPR101-Gs的结构可以识别具有再生潜力的配体
Zhao Yang1, Jun-Yan Wang1,2, Fan Yang1,3,4
1NHC Key Laboratory of Otorhinolaryngology, Qilu Hospital of Shandong University, and Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, China.
Nature chemical biology
|November 9, 2023
概括
研究人员发现了G蛋白结合受体101 (GPR101) 的结构,揭示了它在能量平衡中的作用. 他们确定了小分子激动剂,如AA-14,通过向GPR101.1,证明了其有潜在的再生效应.
科学领域:
- 生物化学 生化学
- 结构生物学 结构生物学
- 药理学 药理学是指药理学的学科.
背景情况:
- G蛋白结合受体101 (GPR101) 是一个孤儿受体,参与能量恒温.
- 了解GPR101的结构对于开发治疗干预措施至关重要.
研究的目的:
- 通过冷电子显微镜,确定GPR101与Gs异构三聚物结合的结构.
- 确定GPR101的潜在小分子激动剂,并评估它们的功能作用.
主要方法:
- 电子显微镜 (cryo-EM) 用于结构的确定.
- 在子选中用于小分子激动剂的识别.
- 在野生类型和缺乏Gpr101的小鼠体内研究,以评估功能影响.
主要成果:
- GPR101-Gs结构揭示了独特的特征,包括细胞外循环2相互作用和疏水激活机制.
- 发现了一种新的侧口袋,促进了四种小分子激动剂的发现,包括AA-14.
- AA-14部分恢复了生长激素/类似胰岛素的生长因子1 (GH/IGF-1) 轴的功能,并对小鼠表现出复原作用.
结论:
- 该研究为GPR101的组成活动提供了结构性基础.
- 像AA-14这样的GPR101激动剂的结构导向识别突出了受体的治疗潜力.
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