The conformational switch in 7-transmembrane receptors: The muscarinic receptor paradigm

Edward C. Hulme*, Zhi Liang Lu, Stuart D.C. Ward, Karen Allman, Carol A.M. Curtis

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

45 Citations (Scopus)

Abstract

The rhodopsin-like superfamily of 7-transmembrane receptors is the largest class of signalling molecules in the mammalian genome. Recently, a combination of mutagenesis, biophysical and modelling studies have suggested a credible model for the α-carbon backbone in the transmembrane region of the 7-transmembrane receptors, and have started to reveal the structural basis of the conformational switch from the inactive to the active state. A key feature may be the replacement of a network of radial constraints, centred on transmembrane helix three, which stabilise the inactive ground state of the receptor by a new set of axial interactions which help to stabilise the activated state. Transmembrane helix three may act as a rotary switch in the activation mechanism. Copyright (C) 1999 Elsevier Science B.V.

Original languageEnglish
Pages (from-to)247-260
Number of pages14
JournalEuropean Journal of Pharmacology
Volume375
Issue number1-3
DOIs
Publication statusPublished - 30 Jun 1999
Externally publishedYes

Keywords

  • 7-Transmembrane receptor
  • Acetylcholine
  • G-protein
  • G-protein coupling pocket
  • Muscarinic receptor

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