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Structure, function and pharmacology of human itch GPCRs
- 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.
- Subjects :
- Models, Molecular
Receptors, Neuropeptide
Agonist
Drug Inverse Agonism
General Science & Technology
medicine.drug_class
Chemical biology
Nerve Tissue Proteins
Endogeny
Peptide
GTP-Binding Protein alpha Subunits, Gi-Go
Pharmacology
Gi-Go
Article
Receptors, G-Protein-Coupled
G-Protein-Coupled
Models
Receptors
medicine
Humans
2.1 Biological and endogenous factors
Aetiology
Receptor
G protein-coupled receptor
Gq-G11
chemistry.chemical_classification
Multidisciplinary
Chemistry
Pruritus
Cryoelectron Microscopy
Pain Research
Antagonist
Molecular
GTP-Binding Protein alpha Subunits
Neuropeptide
Structural biology
GTP-Binding Protein alpha Subunits, Gq-G11
Generic health relevance
Chronic Pain
Subjects
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