Heptares Therapeutics Ltd, BioPark, Broadwater Road, Welwyn Garden City AL7 3AX, UK.
Nature. 2013 Jul 25;499(7459):438-43. doi: 10.1038/nature12357. Epub 2013 Jul 17.
Structural analysis of class B G-protein-coupled receptors (GPCRs), cell-surface proteins that respond to peptide hormones, has been restricted to the amino-terminal extracellular domain, thus providing little understanding of the membrane-spanning signal transduction domain. The corticotropin-releasing factor receptor type 1 is a class B receptor which mediates the response to stress and has been considered a drug target for depression and anxiety. Here we report the crystal structure of the transmembrane domain of the human corticotropin-releasing factor receptor type 1 in complex with the small-molecule antagonist CP-376395. The structure provides detailed insight into the architecture of class B receptors. Atomic details of the interactions of the receptor with the non-peptide ligand that binds deep within the receptor are described. This structure provides a model for all class B GPCRs and may aid in the design of new small-molecule drugs for diseases of brain and metabolism.
B 类 G 蛋白偶联受体(GPCRs)的结构分析一直局限于氨基酸末端细胞外结构域,因此对跨膜信号转导结构域的了解甚少。促肾上腺皮质激素释放因子受体 1 是一种 B 类受体,介导应激反应,被认为是治疗抑郁和焦虑的药物靶点。本文报道了人促肾上腺皮质激素释放因子受体 1 的跨膜结构域与小分子拮抗剂 CP-376395 复合物的晶体结构。该结构提供了对 B 类受体结构的详细了解。描述了受体与结合在受体内部深处的非肽配体相互作用的原子细节。该结构为所有 B 类 GPCR 提供了模型,可能有助于设计用于治疗脑和代谢疾病的新型小分子药物。