G蛋白偶联受体
药物发现
计算生物学
生物
结合位点
受体
小分子
逮捕
化学
细胞生物学
生物化学
作者
H.C. Chan,Yang Li,Thamani Dahoun,Horst Vogel,Shuguang Yuan
标识
DOI:10.1016/j.tibs.2018.11.011
摘要
Many central biological events rely on protein-ligand interactions. The identification and characterization of protein-binding sites for ligands are crucial for the understanding of functions of both endogenous ligands and synthetic drug molecules. G protein-coupled receptors (GPCRs) typically detect extracellular signal molecules on the cell surface and transfer these chemical signals across the membrane, inducing downstream cellular responses via G proteins or β-arrestin. GPCRs mediate many central physiological processes, making them important targets for modern drug discovery. Here, we focus on the most recent breakthroughs in finding new binding sites and binding modes of GPCRs and their potentials for the development of new medicines.
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