The use of constitutively active GPCRs in drug discovery and functional genomics

被引:91
作者
Chalmers, DT [1 ]
Behan, DP [1 ]
机构
[1] Arena Pharmaceut, San Diego, CA 92121 USA
关键词
D O I
10.1038/nrd872
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The complete sequencing of the human genome has afforded researchers the opportunity to identify novel G-protein-coupled receptors (GPCRs) that are expressed in human tissues. The successful identification of hundreds of GPCRs represents the single greatest opportunity for novel drug development today. However, the lack of identified ligands for these GPCRs has limited their utility for traditional drug discovery approaches that focus on ligand-based assay methods to discover and pharmacologically characterize drug candidates. Here, we review the use of constitutively activated GPCRs in the discovery pathway, both as a means to overcome the limitations of traditional drug discovery at novel GPCRs and as a tool to investigate the functionality of these receptors.
引用
收藏
页码:599 / 608
页数:10
相关论文
共 61 条
  • [1] Alewijnse AE, 2000, MOL PHARMACOL, V57, P890
  • [2] Genome engineering via homologous recombination in mouse embryonic stem (ES) cells: an amazingly versatile tool for the study of mammalian biology
    Babinet, C
    Cohen-Tannoudji, M
    [J]. ANAIS DA ACADEMIA BRASILEIRA DE CIENCIAS, 2001, 73 (03): : 365 - 383
  • [3] The conformational change responsible for AT(1) receptor activation is dependent upon two juxtaposed asparagine residues on transmembrane helices III and VII
    Balmforth, AJ
    Lee, AJ
    Warburton, P
    Donnelly, D
    Ball, SG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (07) : 4245 - 4251
  • [4] Behan D P, 2001, Curr Opin Drug Discov Devel, V4, P548
  • [5] BEHAN DP, 1997, Patent No. 9846995
  • [6] CLONING AND EXPRESSION OF A RAT D2 DOPAMINE RECEPTOR CDNA
    BUNZOW, JR
    VANTOL, HHM
    GRANDY, DK
    ALBERT, P
    SALON, J
    CHRISTIE, MJ
    MACHIDA, CA
    NEVE, KA
    CIVELLI, O
    [J]. NATURE, 1988, 336 (6201) : 783 - 787
  • [7] BAY36-7620:: A potent non-competitive mGlu1 receptor antagonist with inverse agonist activity.
    Carroll, FY
    Stolle, A
    Beart, PM
    Voerste, A
    Brabet, I
    Mauler, F
    Joly, C
    Antonicek, H
    Bockaert, J
    Müller, T
    Pin, JP
    Prézau, L
    [J]. MOLECULAR PHARMACOLOGY, 2001, 59 (05) : 965 - 973
  • [8] Melanin-concentrating hormone is the cognate ligand for the orphan G-protein-coupled receptor SLC-1
    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
    [J]. NATURE, 1999, 400 (6741) : 261 - 265
  • [9] Chen G, 2000, MOL PHARMACOL, V57, P125
  • [10] Phe303 in TMVI of the α1B-adrenergic receptor is a key residue coupling TM helical movements to G-protein activation
    Chen, SH
    Lin, F
    Xu, M
    Graham, RM
    [J]. BIOCHEMISTRY, 2002, 41 (02) : 588 - 596