Chemical proteomics and its application to drug discovery

被引:173
作者
Jeffery, DA [1 ]
Bogyo, M [1 ]
机构
[1] Celera Genom, San Francisco, CA 94080 USA
关键词
D O I
10.1016/S0958-1669(02)00010-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The completion of the human genome sequencing project has provided a flood of new information that is likely to change the way scientists approach the study of complex biological, systems. A major challenge lies in translating this information into new and better ways to treat human disease. The multidisciplinary science of chemical proteomics can be used to distill this flood of new information. This approach makes use of synthetic small molecules that can be used to covalently modify a set of related enzymes and subsequently allow their purification and/or identification as valid drug targets. Furthermore, such methods enable rapid biochemical analysis and small-molecule screening of targets thereby accelerating the often difficult process of target validation and drug discovery.
引用
收藏
页码:87 / 95
页数:9
相关论文
共 50 条
  • [1] Proteomic profiling of mechanistically distinct enzyme classes using a common chemotype
    Adam, GC
    Sorensen, EJ
    Cravatt, BF
    [J]. NATURE BIOTECHNOLOGY, 2002, 20 (08) : 805 - 809
  • [2] α-Haloacetophenone derivatives as photoreversible covalent inhibitors of protein tyrosine phosphatases
    Arabaci, G
    Guo, XC
    Beebe, KD
    Coggeshall, KM
    Pei, D
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (21) : 5085 - 5086
  • [3] Defining a link between gap junction communication, proteolysis, and cataract formation
    Baruch, A
    Greenbaum, D
    Levy, ET
    Nielsen, PA
    Gilula, NB
    Kumar, NM
    Bogyo, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (31) : 28999 - 29006
  • [4] Betley JR, 2002, ANGEW CHEM INT EDIT, V41, P775, DOI 10.1002/1521-3773(20020301)41:5<775::AID-ANIE775>3.0.CO
  • [5] 2-F
  • [6] Selective targeting of lysosomal cysteine proteases with radiolabeled electrophilic substrate analogs
    Bogyo, M
    Verhelst, S
    Bellingard-Dubouchaud, V
    Toba, S
    Greenbaum, D
    [J]. CHEMISTRY & BIOLOGY, 2000, 7 (01): : 27 - 38
  • [7] Covalent modification of the active site threonine of proteasomal beta subunits and the Escherichia coli homolog HslV by a new class of inhibitors
    Bogyo, M
    McMaster, JS
    Gaczynska, M
    Tortorella, D
    Goldberg, AL
    Ploegh, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (13) : 6629 - 6634
  • [8] Chemistry-based functional proteomics reveals novel members of the deubiquitinating enzyme
    Borodovsky, A
    Ovaa, H
    Kolli, N
    Gan-Erdene, T
    Wilkinson, KD
    Ploegh, HL
    Kessler, BM
    [J]. CHEMISTRY & BIOLOGY, 2002, 9 (10): : 1149 - 1159
  • [9] A novel active site-directed probe specific for deubiquitylating enzymes reveals proteasome association of USP14
    Borodovsky, A
    Kessler, BM
    Casagrande, R
    Overkleeft, HS
    Wilkinson, KD
    Ploegh, HL
    [J]. EMBO JOURNAL, 2001, 20 (18) : 5187 - 5196
  • [10] Applied genomics: integration of the technology within pharmaceutical research and development
    Cockett, M
    Dracopoli, N
    Sigal, E
    [J]. CURRENT OPINION IN BIOTECHNOLOGY, 2000, 11 (06) : 602 - 609