The impact of genomics on drug discovery

被引:76
作者
Debouck, C [1 ]
Metcalf, B [1 ]
机构
[1] SmithKline Beecham Pharmaceut, Discovery Chem & Platform Technol, Res & Dev, King Of Prussia, PA 19406 USA
关键词
EST; cathepsin K; G-protein coupled receptors; microarrays; proteomics;
D O I
10.1146/annurev.pharmtox.40.1.193
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
High-throughput gene sequencing has revolutionized the process used to identify novel molecular targets for drug discovery. Thousands of new gene sequences have been generated but only a limited number of these can be converted into validated targets likely to be involved in disease. We describe here some of the approaches used at SmithKline Beecham to select and validate novel targets. These include the identification of selective tissue gene product expression, such as for cathepsin K, a novel osteoclast-specific cysteine protease. We also describe the discovery and functional characterization of novel members of the G-protein coupled receptor superfamily and their pairing with natural ligands. Lastly, we discuss the promises of gene microarrays and proteomics, developing technologies that allow the parallel analyses of tissue expression patterns of thousands of genes or proteins, respectively.
引用
收藏
页码:193 / 207
页数:15
相关论文
共 38 条
[1]   COMPLEMENTARY-DNA SEQUENCING - EXPRESSED SEQUENCE TAGS AND HUMAN GENOME PROJECT [J].
ADAMS, MD ;
KELLEY, JM ;
GOCAYNE, JD ;
DUBNICK, M ;
POLYMEROPOULOS, MH ;
XIAO, H ;
MERRIL, CR ;
WU, A ;
OLDE, B ;
MORENO, RF ;
KERLAVAGE, AR ;
MCCOMBIE, WR ;
VENTER, JC .
SCIENCE, 1991, 252 (5013) :1651-1656
[2]   Analysis of EST-driven gene annotation in human genomic sequence [J].
Bailey, LC ;
Searls, DB ;
Overton, GC .
GENOME RESEARCH, 1998, 8 (04) :362-376
[3]   Proteomics: quantitative and physical mapping of cellular proteins [J].
Blackstock, WP ;
Weir, MP .
TRENDS IN BIOTECHNOLOGY, 1999, 17 (03) :121-127
[4]   Proteolytic activity of human osteoclast cathepsin K - Expression, purification, activation, and substrate identification [J].
Bossard, MJ ;
Tomaszek, TA ;
Thompson, SK ;
Amegadzie, BY ;
Hanning, CR ;
Jones, C ;
Kurdyla, JT ;
McNulty, DE ;
Drake, FH ;
Gowen, M ;
Levy, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (21) :12517-12524
[5]   Regulatory elements and expression profiles [J].
Bucher, P .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1999, 9 (03) :400-407
[6]   Genome sequence of the nematode C-elegans:: A platform for investigating biology [J].
不详 .
SCIENCE, 1998, 282 (5396) :2012-2018
[7]   Melanin-concentrating hormone is the cognate ligand for the orphan G-protein-coupled receptor SLC-1 [J].
Chambers, J ;
Ames, RS ;
Bergsma, D ;
Muir, A ;
Fitzgerald, LR ;
Hervieu, G ;
Dytko, GM ;
Foley, JJ ;
Martin, J ;
Liu, WS ;
Park, J ;
Ellis, C ;
Ganguly, S ;
Konchar, S ;
Cluderay, J ;
Leslie, R ;
Wilson, S ;
Sarau, HM .
NATURE, 1999, 400 (6741) :261-265
[8]  
CHENERA B, 1995, J AM CHEM SOC, V117, P11999
[9]  
CHIU AT, 1990, J PHARMACOL EXP THER, V252, P711
[10]   EVOLUTION OF A NOVEL SERIES OF [(N,N-DIMETHYLAMINO)PROPYL]ANILIDE AND PIPERAZINYLBENZANILIDES AS THE FIRST SELECTIVE 5-HT1D ANTAGONISTS [J].
CLITHEROW, JW ;
SCOPES, DIC ;
SKINGLE, M ;
JORDAN, CC ;
FENIUK, W ;
CAMPBELL, IB ;
CARTER, MC ;
COLLINGTON, EW ;
CONNOR, HE ;
HIGGINS, GA ;
BEATTIE, D ;
KELLY, HA ;
MITCHELL, WL ;
OXFORD, AW ;
WADSWORTH, AH ;
TYERS, MB .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (15) :2253-2257