Abstract
GPCRs exhibit a common architecture of seven transmembrane helices (TMs) linked by intracellular loops and extracellular loops (ECLs). Given their peripheral location to the site of G-protein interaction, it might be assumed that ECL segments merely link the important TMs within the helical bundle of the receptor. However, compelling evidence has emerged in recent years revealing a critical role for ECLs in many fundamental aspects of GPCR function, which supported by recent GPCR crystal structures has provided mechanistic insights. This review will present current understanding of the key roles of ECLs in ligand binding, activation and regulation of both family A and family B GPCRs. LINKED ARTICLES This article is part of a themed section on the Molecular Pharmacology of G Protein-Coupled Receptors (GPCRs).
Original language | English |
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Pages (from-to) | 1688-1703 |
Number of pages | 16 |
Journal | British Journal of Pharmacology |
Volume | 165 |
Issue number | 6 |
Early online date | 22 Aug 2011 |
DOIs | |
Publication status | Published - Mar 2012 |
Externally published | Yes |
Bibliographical note
free accessKeywords
- extracellular loop
- family A GPCR
- family B GPCR
- G-protein coupled receptor
- ligand binding
- receptor activation
ASJC Scopus subject areas
- Pharmacology