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

Citation
Ec. Hulme et al., The conformational switch in 7-transmembrane receptors: the muscarinic receptor paradigm, EUR J PHARM, 375(1-3), 1999, pp. 247-260
Citations number
83
Categorie Soggetti
Pharmacology & Toxicology
Journal title
EUROPEAN JOURNAL OF PHARMACOLOGY
ISSN journal
00142999 → ACNP
Volume
375
Issue
1-3
Year of publication
1999
Pages
247 - 260
Database
ISI
SICI code
0014-2999(19990630)375:1-3<247:TCSI7R>2.0.ZU;2-G
Abstract
The rhodopsin-like superfamily of 7-transmembrane receptors is the largest class of signalling molecules in the mammalian genome. Recently, a combinat ion of mutagenesis, biophysical and modelling studies have suggested a cred ible model for the alpha-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 an 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 t he activation mechanism. (C) 1999 Elsevier Science B.V. All rights reserved .