Literature DB >> 30522088

Hot spots for GPCR signaling: lessons from single-molecule microscopy.

Davide Calebiro1, Marie-Lise Jobin2.   

Abstract

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.
Copyright © 2018 Elsevier Ltd. All rights reserved.

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Year:  2018        PMID: 30522088     DOI: 10.1016/j.ceb.2018.11.003

Source DB:  PubMed          Journal:  Curr Opin Cell Biol        ISSN: 0955-0674            Impact factor:   8.382


  4 in total

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Journal:  Cells       Date:  2019-05-14       Impact factor: 6.600

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Journal:  Angew Chem Int Ed Engl       Date:  2020-01-07       Impact factor: 16.823

3.  The Gαi protein subclass selectivity to the dopamine D2 receptor is also decided by their location at the cell membrane.

Authors:  Agnieszka Polit; Beata Rysiewicz; Paweł Mystek; Ewa Błasiak; Marta Dziedzicka-Wasylewska
Journal:  Cell Commun Signal       Date:  2020-12-11       Impact factor: 5.712

4.  Efficient G protein coupling is not required for agonist-mediated internalization and membrane reorganization of the adenosine A3 receptor.

Authors:  Leigh A Stoddart; Laura E Kilpatrick; Ross Corriden; Barrie Kellam; Stephen J Briddon; Stephen J Hill
Journal:  FASEB J       Date:  2021-04       Impact factor: 5.834

  4 in total

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