Multiplex GPCR assay in reverse transfection cell microarrays

被引:28
作者
Mishina, YM [1 ]
Wilson, CJ [1 ]
Bruett, L [1 ]
Smith, JJ [1 ]
Stoop-Myer, C [1 ]
Jong, S [1 ]
Amaral, LP [1 ]
Pedersen, R [1 ]
Lyman, SK [1 ]
Myer, VE [1 ]
Kreider, BL [1 ]
Thompson, CM [1 ]
机构
[1] Akceli Inc, Medford, MA 02155 USA
关键词
reverse transfection; cell microarray; multiplexed assay; GPCR drug discovery; GPCR de-orphaning;
D O I
10.1177/1087057103261880
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
G protein-coupled receptors (GPCRs) are a superfamily of proteins that include some of the most important drug targets in the pharmaceutical industry. Despite the success of this group of drugs, there remains a need to identify GPCR-targeted drugs with greater selectivity, to develop screening assays for validated targets, and to identify ligands for orphan receptors. To address these challenges, the authors have created a multiplexed GPCR assay that measures greater than 3000 receptor:ligand interactions in a single microplate. The multiplexed assay is generated by combining reverse transfection in a 96-well plate format with a calcium flux readout. This assay quantitatively measures receptor activation and inhibition and permits the determination of compound potency and selectivity for entire families of GPCRs in parallel. To expand the number of GPCR targets that may be screened in this system, receptors are cotransfected with plasmids encoding a promiscuous G protein, permitting the analysis of receptors that do not normally mobilize intracellular calcium upon activation. The authors demonstrate the utility of reverse transfection cell microarrays to GPCR-targeted drug discovery with examples of ligand selectivity screening against a panel of GPCRs as well as dose-dependent titrations of selected agonists and antagonists.
引用
收藏
页码:196 / 207
页数:12
相关论文
共 31 条
[21]  
Mody SM, 2000, MOL PHARMACOL, V57, P13
[22]   G protein pathways [J].
Neves, SR ;
Ram, PT ;
Iyengar, R .
SCIENCE, 2002, 296 (5573) :1636-1639
[23]   G-ALPHA(15) AND G-ALPHA(16) COUPLE A WIDE VARIETY OF RECEPTORS TO PHOSPHOLIPASE-C [J].
OFFERMANNS, S ;
SIMON, MI .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (25) :15175-15180
[24]  
SANDMANN J, 1991, J BIOL CHEM, V266, P6031
[25]   Effects of a range of β2 adrenoceptor agonists on changes in intracellular cyclic AMP and on cyclic AMP driven gene expression in cultured human airway smooth muscle cells [J].
Scott, MGH ;
Swan, C ;
Jobson, TM ;
Rees, S ;
Hall, IP .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 128 (03) :721-729
[26]   The G protein-coupled receptor repertoires of human and mouse [J].
Vassilatis, DK ;
Hohmann, JG ;
Zeng, H ;
Li, FS ;
Ranchalis, JE ;
Mortrud, MT ;
Brown, A ;
Rodriguez, SS ;
Weller, JR ;
Wright, AC ;
Bergmann, JE ;
Gaitanaris, GA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (08) :4903-4908
[27]  
WATLING KJ, 2001, SIGMA RBI HDB RECEPT
[28]   Target validation of G-protein coupled receptors [J].
Wise, A ;
Gearing, K ;
Rees, S .
DRUG DISCOVERY TODAY, 2002, 7 (04) :235-246
[29]   α1-adrenergic stimulation of sarcolemmal Na+-H+ exchanger activity in rat ventricular myocytes -: Evidence for selective mediation by the α1A-adrenoceptor subtype [J].
Yokoyama, H ;
Yasutake, M ;
Avkiran, M .
CIRCULATION RESEARCH, 1998, 82 (10) :1078-1085
[30]   Microarrays of cells expressing defined cDNAs [J].
Ziauddin, J ;
Sabatini, DM .
NATURE, 2001, 411 (6833) :107-110