Towards structural models of molecular recognition in olfactory receptors

被引:19
作者
Afshar, M
Hubbard, RE
Demaille, J
机构
[1] CNRS, CRBM, F-34033 Montpellier, France
[2] Univ York, Dept Chem, York YO1 5DD, N Yorkshire, England
关键词
molecular docking; G protein coupled receptor; protein ligand interaction; olfaction; molecular modelling;
D O I
10.1016/S0300-9084(98)80019-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The G protein coupled receptors (GPCR) are an important class of proteins that act as signal transducers through the cytoplasmic membrane. Understanding the structure and activation mechanism of these proteins is crucial for understanding many different aspects of cellular signalling. The olfactory receptors correspond to the largest family of GPCRs. Very little is known about how the structures of the receptors govern the specificity of interaction which enables identification of particular odorant molecules. In this paper, we review recent developments in two areas of molecular modelling: methods for modelling the configuration of trans-membrane helices and methods for automatic docking of ligands into receptor structures. We then show how a subset of these methods can be combined to construct a model of a rat odorant receptor interacting with lyral for which experimental data are available. This modelling can help us make progress towards elucidating the specificity of interactions between receptors and odorant molecules. ((C) Societe francaise de biochimie et biologie moleculaire/Elsevier, Paris).
引用
收藏
页码:129 / 135
页数:7
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