在Ca2+感应受体的Allosteric调制和G蛋白选择性
Feng He1, Cheng-Guo Wu1, Yang Gao1,2
1Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA, USA.
Nature
|February 7, 2024
概括
感应受体 (CaSR) 的结构揭示了它如何激活G蛋白并对像cinacalcet这样的药物做出反应. 多胺和L-三也通过不同的机制调节CaSR活性.
科学领域:
- 生物化学 生物化学
- 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:
- 感应受体 (CaSR) 是一个GPCR,对稳定至关重要.
- 了解CaSR激活机制对于治疗与有关的疾病至关重要.
研究的目的:
- 阐明人类CaSR激活的结构基础及其与G蛋白 (Gi和Gq) 的选择性合.
- 为了研究CaSR通过cinacalcet,多胺和L-酸盐的全调节.
主要方法:
- 低温电子显微镜 (cryo-EM) 用于确定CaSR.的高分辨率结构.
- 功能性测试用于评估G蛋白合和受体激活.
- 在脂质纳米光盘中对CaSR的研究.
主要成果:
- 由Gi和Gq激活CaSR涉及7TM域和蛋白质-脂质相互作用中的构造变化.
- 选择性G蛋白合是由细胞内循环和C端的重排调解的.
- 多氨酸通过稳定原体之间的相互作用来增强CaSR激活.
- L-托和cinacalcet与7TM捆中的重叠位点结合,作为全调节剂.
结论:
- 为CaSR G-蛋白激活和选择性提供了一个结构框架.
- 揭示了内源和外源CaSR调节器的独特结合点和机制.
- 提供了关于GPCRs通过小分子和天然配体的全调节的见解.
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