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Structure, function and pharmacology of human itch GPCRs

Authors :
Samuel T. Slocum
Yongfeng Liu
Bryan L. Roth
Jian Jin
Brian E. Krumm
Brian J. Bender
Reid H.J. Olsen
Hye Jin Kang
Justin G. English
Isha Singh
Jing Liu
Lily Yeh Jan
Wenlei Ye
Brian K. Shoichet
Xi Ping Huang
Byron W. Hayes
Can Cao
John D. McCorvy
Jonathan F. Fay
Katherine Lansu
Soman N. Abraham
Shicheng Zhang
Chengwei Zhang
Wesley K. Kroeze
Kuglae Kim
He Chen
Ryan H. Gumpper
Jeffrey F. DiBerto
Joel Karpiak
Source :
Nature, Nature, vol 600, iss 7887
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Abstract

The MRGPRX family of receptors (MRGPRX1–4) is a family of mas-related G-protein-coupled receptors that have evolved relatively recently1. Of these, MRGPRX2 and MRGPRX4 are key physiological and pathological mediators of itch and related mast cell-mediated hypersensitivity reactions2–5. MRGPRX2 couples to both Gi and Gq in mast cells6. Here we describe agonist-stabilized structures of MRGPRX2 coupled to Gi1 and Gq in ternary complexes with the endogenous peptide cortistatin-14 and with a synthetic agonist probe, respectively, and the development of potent antagonist probes for MRGPRX2. We also describe a specific MRGPRX4 agonist and the structure of this agonist in a complex with MRGPRX4 and Gq. Together, these findings should accelerate the structure-guided discovery of therapeutic agents for pain, itch and mast cell-mediated hypersensitivity. Structural studies of the itch receptors MRGPRX2 and MRGPRX4 in complex with endogenous and synthetic ligands provide a basis for the development of therapeutic compounds for pain, itch and mast cell-mediated hypersensitivity.

Details

ISSN :
14764687 and 00280836
Volume :
600
Database :
OpenAIRE
Journal :
Nature
Accession number :
edsair.doi.dedup.....70e74bb609d8bd744fc782cf9ab54a3d
Full Text :
https://doi.org/10.1038/s41586-021-04126-6