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Structure, function and pharmacology of human itch GPCRs.

Authors :
Cao C
Kang HJ
Singh I
Chen H
Zhang C
Ye W
Hayes BW
Liu J
Gumpper RH
Bender BJ
Slocum ST
Krumm BE
Lansu K
McCorvy JD
Kroeze WK
English JG
DiBerto JF
Olsen RHJ
Huang XP
Zhang S
Liu Y
Kim K
Karpiak J
Jan LY
Abraham SN
Jin J
Shoichet BK
Fay JF
Roth BL
Source :
Nature [Nature] 2021 Dec; Vol. 600 (7887), pp. 170-175. Date of Electronic Publication: 2021 Nov 17.
Publication Year :
2021

Abstract

The MRGPRX family of receptors (MRGPRX1-4) is a family of mas-related G-protein-coupled receptors that have evolved relatively recently <superscript>1</superscript> . Of these, MRGPRX2 and MRGPRX4 are key physiological and pathological mediators of itch and related mast cell-mediated hypersensitivity reactions <superscript>2-5</superscript> . MRGPRX2 couples to both G <subscript>i</subscript> and G <subscript>q</subscript> in mast cells <superscript>6</superscript> . Here we describe agonist-stabilized structures of MRGPRX2 coupled to G <subscript>i1</subscript> and G <subscript>q</subscript> 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 G <subscript>q</subscript> . Together, these findings should accelerate the structure-guided discovery of therapeutic agents for pain, itch and mast cell-mediated hypersensitivity.<br /> (© 2021. The Author(s), under exclusive licence to Springer Nature Limited.)

Details

Language :
English
ISSN :
1476-4687
Volume :
600
Issue :
7887
Database :
MEDLINE
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
34789874
Full Text :
https://doi.org/10.1038/s41586-021-04126-6