Center for Structural Pharmacology and Therapeutics Development, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou 310016, China.
Key Laboratory Experimental Teratology of the Ministry of Education and Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.
Mol Cell. 2024 Feb 1;84(3):570-583.e7. doi: 10.1016/j.molcel.2023.12.020. Epub 2024 Jan 11.
Adhesion G protein-coupled receptors (aGPCRs) are evolutionarily ancient receptors involved in a variety of physiological and pathophysiological processes. Modulators of aGPCR, particularly antagonists, hold therapeutic promise for diseases like cancer and immune and neurological disorders. Hindered by the inactive state structural information, our understanding of antagonist development and aGPCR activation faces challenges. Here, we report the cryo-electron microscopy structures of human CD97, a prototypical aGPCR that plays crucial roles in immune system, in its inactive apo and G13-bound fully active states. Compared with other family GPCRs, CD97 adopts a compact inactive conformation with a constrained ligand pocket. Activation induces significant conformational changes for both extracellular and intracellular sides, creating larger cavities for Stachel sequence binding and G13 engagement. Integrated with functional and metadynamics analyses, our study provides significant mechanistic insights into the activation and signaling of aGPCRs, paving the way for future drug discovery efforts.
黏附 G 蛋白偶联受体(aGPCR)是一类古老的受体,参与多种生理和病理生理过程。aGPCR 的调节剂,特别是拮抗剂,为癌症以及免疫和神经紊乱等疾病提供了治疗的希望。由于无活性状态结构信息的阻碍,我们在了解拮抗剂开发和 aGPCR 激活方面面临挑战。在这里,我们报告了人类 CD97 的冷冻电镜结构,CD97 是一种典型的 aGPCR,在免疫系统中发挥关键作用,处于无配体的apo 态和与 G13 结合的完全激活态。与其他家族的 GPCR 相比,CD97 采用紧凑的无活性构象,配体口袋受到限制。激活诱导细胞外和细胞内两侧发生显著的构象变化,为 Stachel 序列结合和 G13 结合创造了更大的腔。与功能和元动力学分析相结合,我们的研究为 aGPCR 的激活和信号转导提供了重要的机制见解,为未来的药物发现工作铺平了道路。