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
相关论文
共 42 条
[1]   Pharmacological characterization of type 1 alpha metabotropic glutamate receptor-stimulated [S-35]-GTP gamma S binding [J].
Akam, EC ;
Carruthers, AM ;
Nahorski, SR ;
Challiss, RAJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 121 (06) :1203-1209
[2]   IDENTIFICATION OF EFFECTOR-ACTIVATING RESIDUES OF GS-ALPHA [J].
BERLOT, CH ;
BOURNE, HR .
CELL, 1992, 68 (05) :911-922
[3]   Induction of NFAT-mediated transcription by G(q)-coupled receptors in lymphoid and non-lymphoid cells [J].
Boss, V ;
Talpade, DJ ;
Murphy, TJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (18) :10429-10432
[4]   How receptors talk to trimeric G proteins [J].
Bourne, HR .
CURRENT OPINION IN CELL BIOLOGY, 1997, 9 (02) :134-142
[5]  
Burstein ES, 1997, J NEUROCHEM, V68, P525
[6]   G protein beta gamma subunits [J].
Clapham, DE ;
Neer, EJ .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1997, 37 :167-203
[7]   How G proteins work: A continuing story [J].
Coleman, DE ;
Sprang, SR .
TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (02) :41-44
[8]   SUBSTITUTION OF 3 AMINO-ACIDS SWITCHES RECEPTOR SPECIFICITY OF G(Q)ALPHA TO THAT OF G(I)ALPHA [J].
CONKLIN, BR ;
FARFEL, Z ;
LUSTIG, KD ;
JULIUS, D ;
BOURNE, HR .
NATURE, 1993, 363 (6426) :274-276
[9]  
Conklin BR, 1996, MOL PHARMACOL, V50, P885
[10]   Controlling signaling with a specifically designed Gi-coupled receptor [J].
Coward, P ;
Wada, HG ;
Falk, MS ;
Chan, SDH ;
Meng, F ;
Akil, H ;
Conklin, BR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (01) :352-357