Sign in
BiophysicsCell Discovery
Peer-reviewed journal article

Structure basis for recognition of 26RFa by the pyroglutamylated RFamide peptide receptor

Sanshan JiniD, Shimeng GuoiD, Youwei XuiD, Xin Li, Canrong WuiD, Xinheng HeiD, Benxun PaniD, Wenwen Xin, Heng ZhangiD, Wen HuiD, Yu-Ling Yin, Tianwei ZhangiD, Kai Wu, Qingning YuaniD, H. Eric XuiD, Xin XieiD, Yi JiangiD

Abstract

The neuropeptide 26RFa, a member of the RF-amide peptide family, activates the pyroglutamylated RF-amide peptide receptor (QRFPR), a class A GPCR. The 26RFa/QRFPR system plays critical roles in energy homeostasis, making QRFPR an attractive drug target for treating obesity, diabetes, and eating disorders. However, the lack of structural information has hindered our understanding of the peptide recognition and regulatory mechanism of QRFPR, impeding drug design efforts. In this study, we determined the cryo-EM structure of the Gq-coupled QRFPR bound to 26RFa. The structure reveals a unique assembly mode of the receptor extracellular regions and the peptide N-terminus and elucidates the recognition mechanism of the C-terminal heptapeptide of 26RFa within the transmembrane binding pocket of QRFPR. The study also clarifies the similarities and distinctions in the binding pattern of the RF-amide moiety in five RF-amide peptides and the RY-amide segment in neuropeptide Y. These findings deepen our understanding of the RF-amide peptides recognition, aiding in the rational design of drugs targeting QRFPR and other RF-amide receptors.

PDFDOI

02 /Specification & Classification

Click any tag to browse matching papers
Citations
9
FWCI
1.00
Field percentile
top 29%

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.