Hot spots for GPCR signaling: lessons from single-molecule microscopy.
Journal
Current opinion in cell biology
ISSN: 1879-0410
Titre abrégé: Curr Opin Cell Biol
Pays: England
ID NLM: 8913428
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
received:
18
10
2018
revised:
05
11
2018
accepted:
07
11
2018
pubmed:
7
12
2018
medline:
18
1
2020
entrez:
7
12
2018
Statut:
ppublish
Résumé
G protein-coupled receptors (GPCRs) are among the best-studied membrane receptors, mainly due to their central role in human physiology, involvement in disease and relevance as drug targets. Although biochemical and pharmacological studies have characterized the main steps in GPCR signaling, how GPCRs produce highly specific responses in our cells remains insufficiently understood. New developments in single-molecule microscopy have made it possible to study the protein-protein interactions at the basis of GPCR signaling in previously inconceivable detail. Using this approach, it was recently possible to follow individual receptors and G proteins as they diffuse, interact and signal on the surface of living cells. This has revealed hot spots on the plasma membrane, where receptors and G proteins undergo transient interactions to produce rapid and local signals. Overall, these recent findings reveal a high degree of dynamicity and complexity in signaling by GPCRs, which provides a new basis to understand how these important receptors produce specific effects and might pave the way to innovative pharmacological approaches.
Identifiants
pubmed: 30522088
pii: S0955-0674(18)30101-7
doi: 10.1016/j.ceb.2018.11.003
pii:
doi:
Substances chimiques
Receptors, G-Protein-Coupled
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
57-63Informations de copyright
Copyright © 2018 Elsevier Ltd. All rights reserved.