Chimaeric Gα proteins:: their potential use in drug discovery

被引:77
作者
Milligan, G
Rees, S
机构
[1] Univ Glasgow, Glasgow G12 8QQ, Lanark, Scotland
[2] Glaxo Wellcome Res & Dev Ltd, Receptor Syst Unit, Stevenage SG1 2NY, Herts, England
基金
英国惠康基金;
关键词
D O I
10.1016/S0165-6147(99)01320-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Approaches that allow ligand occupancy of a wide range of G protein-coupled receptors to be converted into robust assays amenable to relatively high-throughput analysis are ideal for screening for novel ligands at this class of receptor. Many attempts have been made to design universal ligand-screening systems such that any GPCR can be screened using a common assay end-point. Manipulation of the G protein within the assay system offers the possibility of achieving this. To better understand the domains involved in the interactions between G protein-coupled receptors. G proteins and effector polypeptides and the fine details of these contacts, a wide range of chimaeric G protein cr subunits have been produced. Graeme Milligan and Stephen Rees discuss the information generated by such studies and the ways in which such chimaeric G proteins can be integrated into assay systems for drug discovery.
引用
收藏
页码:118 / 124
页数:7
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