G蛋白偶联受体
生物
受体
计算生物学
信号转导
配对
细胞生物学
遗传学
超导电性
物理
量子力学
作者
Simon R. Foster,Alexander S. Hauser,Line Vedel,Ryan T. Strachan,Xi‐Ping Huang,Ariana C. Gavin,Sushrut D. Shah,Ajay P. Nayak,Linda M. Haugaard‐Kedström,Raymond B. Penn,Bryan L. Roth,Hans Bräuner‐Osborne,David E. Gloriam
出处
期刊:Cell
[Cell Press]
日期:2019-10-01
卷期号:179 (4): 895-908.e21
被引量:230
标识
DOI:10.1016/j.cell.2019.10.010
摘要
The peptidergic system is the most abundant network of ligand-receptor-mediated signaling in humans. However, the physiological roles remain elusive for numerous peptides and more than 100 G protein-coupled receptors (GPCRs). Here we report the pairing of cognate peptides and receptors. Integrating comparative genomics across 313 species and bioinformatics on all protein sequences and structures of human class A GPCRs, we identify universal characteristics that uncover additional potential peptidergic signaling systems. Using three orthogonal biochemical assays, we pair 17 proposed endogenous ligands with five orphan GPCRs that are associated with diseases, including genetic, neoplastic, nervous and reproductive system disorders. We also identify additional peptides for nine receptors with recognized ligands and pathophysiological roles. This integrated computational and multifaceted experimental approach expands the peptide-GPCR network and opens the way for studies to elucidate the roles of these signaling systems in human physiology and disease. VIDEO ABSTRACT.
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