Allostery in GPCRs: 'MWC' revisited

Research output: Contribution to journalArticleResearchpeer-review

Abstract

G protein-coupled receptors (GPCRs) constitute the largest family of receptors in the genome and are the targets for at least 30 of current medicines. In recent years, there has been a dramatic increase in the discovery of allosteric modulators of GPCR activity and a growing appreciation of the diverse modes by which GPCRs can be regulated by both orthosteric and allosteric ligands. Interestingly, some of the contemporary views of GPCR function reflect characteristics that are shared by prototypical allosteric proteins, as encompassed in the classic Monod-Wyman-Changeux (MWC) model initially proposed for enzymes and subsequently extended to other protein families. In this review, we revisit the MWC model in the context of emerging structural, functional and operational data on GPCR allostery.
Original languageEnglish
Pages (from-to)663 - 672
Number of pages10
JournalTrends in Biochemical Sciences
Volume36
Issue number12
DOIs
Publication statusPublished - 2011

Cite this

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Allostery in GPCRs: 'MWC' revisited. / Canals, Meritxell; Sexton, Patrick; Christopoulos, Arthur.

In: Trends in Biochemical Sciences, Vol. 36, No. 12, 2011, p. 663 - 672.

Research output: Contribution to journalArticleResearchpeer-review

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