CAS Key Laboratory of Quantitative Engineering Biology, Institute of Synthetic Biology, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.
iHuman Institute, ShanghaiTech University, 393 Middle Huaxia Road, Pudong, Shanghai, 201210, China.
Adv Sci (Weinh). 2024 Apr;11(14):e2306311. doi: 10.1002/advs.202306311. Epub 2024 Jan 31.
The G-protein-coupled human cannabinoid receptor 1 (CB1) is a promising therapeutic target for pain management, inflammation, obesity, and substance abuse disorders. The structures of CB1-G complexes in synthetic agonist-bound forms have been resolved to date. However, the commercial drug recognition and G coupling mechanisms of CB1 remain elusive. Herein, the cryo-electron microscopy (cryo-EM) structure of CB1-G complex, in fenofibrate-bound form, at near-atomic resolution, is reported. The structure elucidates the delicate mechanisms of the precise fenofibrate recognition and G protein coupling by CB1 and will facilitate future drug discovery and design.
G 蛋白偶联的人体大麻素受体 1(CB1)是疼痛管理、炎症、肥胖和物质滥用障碍的有前途的治疗靶点。迄今为止,已经解析了与合成激动剂结合的 CB1-G 复合物的结构。然而,CB1 的商业药物识别和 G 偶联机制仍然难以捉摸。本文报道了近原子分辨率下,与非诺贝特结合形式的 CB1-G 复合物的低温电子显微镜(cryo-EM)结构。该结构阐明了 CB1 精确识别非诺贝特和与 G 蛋白偶联的微妙机制,并将促进未来的药物发现和设计。