Ligand recognition mechanism of the human relaxin family peptide receptor 4 (RXFP4)

• Published in: Nature communications Vol. 14; no. 1; p. 492
• Main Authors: Chen, Yan, Zhou, Qingtong, Wang, Jiang, Xu, Youwei, Wang, Yun, Yan, Jiahui, Wang, Yibing, Zhu, Qi, Zhao, Fenghui, Li, Chenghao, Chen, Chuan-Wei, Cai, Xiaoqing, Bathgate, Ross A D, Shen, Chun, Eric Xu, H, Yang, Dehua, Liu, Hong, Wang, Ming-Wei
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 30.01.2023; Nature Publishing Group UK; Nature Portfolio
• Subjects: Binding; Biological activity; Chains; Cryoelectron Microscopy; Electron microscopy; G protein-coupled receptors; Growth factors; Humans; Insulin; Insulin - metabolism; Insulin-like growth factors; Ligands; Mutagenesis; Peptides; Proteins; Receptors; Receptors, G-Protein-Coupled - chemistry; Receptors, Peptide - chemistry; Receptors, Peptide - genetics; Recognition; Relaxin; Relaxin - metabolism; Selectivity; Signal Transduction
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-023-36182-z

Members of the insulin superfamily regulate pleiotropic biological processes through two types of target-specific but structurally conserved peptides, insulin/insulin-like growth factors and relaxin/insulin-like peptides. The latter bind to the human relaxin family peptide receptors (RXFPs). Here, we report three cryo-electron microscopy structures of RXFP4-G protein complexes in the presence of the endogenous ligand insulin-like peptide 5 (INSL5) or one of the two small molecule agonists, compound 4 and DC591053. The B chain of INSL5 adopts a single α-helix that penetrates into the orthosteric pocket, while the A chain sits above the orthosteric pocket, revealing a peptide-binding mode previously unknown. Together with mutagenesis and functional analyses, the key determinants responsible for the peptidomimetic agonism and subtype selectivity were identified. Our findings not only provide insights into ligand recognition and subtype selectivity among class A G protein-coupled receptors, but also expand the knowledge of signaling mechanisms in the insulin superfamily.