Profiling protein function with small molecule microarrays

被引:130
作者
Winssinger, N
Ficarro, S
Schultz, PG
Harris, JL
机构
[1] Novartis Res Fdn, San Diego, CA 92121 USA
[2] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[3] Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
关键词
D O I
10.1073/pnas.172286899
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The regulation of protein function through posttranslational modification, local environment, and protein-protein interaction is critical to cellular function. The ability to analyze on a genome-wide scale protein functional activity rather than changes in protein abundance or structure would provide important new insights into complex biological processes. Herein, we report the application of a spatially addressable small molecule microarray to an activity-based profile of proteases in crude cell lysates. The potential of this small molecule-based profiling technology is demonstrated by the detection of caspase activation upon induction of apoptosis, characterization of the activated caspase, and inhibition of the caspase-executed apoptotic phenotype using the small molecule inhibitor identified in the microarray-based profile.
引用
收藏
页码:11139 / 11144
页数:6
相关论文
共 33 条
  • [1] Profiling the specific reactivity of the proteome with non-directed activity-based probes
    Adam, GC
    Cravatt, BF
    Sorensen, EJ
    [J]. CHEMISTRY & BIOLOGY, 2001, 8 (01): : 81 - 95
  • [2] Mass spectrometry in proteomics
    Aebersold, R
    Goodlett, DR
    [J]. CHEMICAL REVIEWS, 2001, 101 (02) : 269 - 295
  • [3] DeRisi J, 1996, NAT GENET, V14, P457
  • [4] Delineation of prognostic biomarkers in prostate cancer
    Dhanasekaran, SM
    Barrette, TR
    Ghosh, D
    Shah, R
    Varambally, S
    Kurachi, K
    Pienta, KJ
    Rubin, MA
    Chinnaiyan, AM
    [J]. NATURE, 2001, 412 (6849) : 822 - 826
  • [5] Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 1. Michael acceptor structure-activity studies
    Dragovich, PS
    Webber, SE
    Babine, RE
    Fuhrman, SA
    Patick, AK
    Matthews, DA
    Lee, CA
    Reich, SH
    Prins, TJ
    Marakovits, JT
    Littlefield, ES
    Zhou, R
    Tikhe, J
    Ford, CE
    Wallace, MB
    Meador, JW
    Ferre, RA
    Brown, EL
    Binford, SL
    Harr, JEV
    DeLisle, DM
    Worland, ST
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (15) : 2806 - 2818
  • [6] AN APPROACH TO CORRELATE TANDEM MASS-SPECTRAL DATA OF PEPTIDES WITH AMINO-ACID-SEQUENCES IN A PROTEIN DATABASE
    ENG, JK
    MCCORMACK, AL
    YATES, JR
    [J]. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (11) : 976 - 989
  • [7] New paradigm for lymphocyte granule-mediated cytotoxicity - Target cells bind and internalize granzyme B, but an endosomolytic agent is necessary for cytosolic delivery and subsequent apoptosis
    Froelich, CJ
    Orth, K
    Turbov, J
    Seth, P
    Gottlieb, R
    Babior, B
    Shah, GM
    Bleackley, RC
    Dixit, VM
    Hanna, W
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (46) : 29073 - 29079
  • [8] FACILE REDUCTION OF ETHYL THIOL ESTERS TO ALDEHYDES - APPLICATION TO A TOTAL SYNTHESIS OF (+)-NEOTHRAMYCIN-A METHYL-ETHER
    FUKUYAMA, T
    LIN, SC
    LI, LP
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (19) : 7050 - 7051
  • [9] Rapid and general profiling of protease specificity by using combinatorial fluorogenic substrate libraries
    Harris, JL
    Backes, BJ
    Leonetti, F
    Mahrus, S
    Ellman, JA
    Craik, CS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (14) : 7754 - 7759
  • [10] Substrate specificity of the human proteasome
    Harris, JL
    Alper, PB
    Li, J
    Rechsteiner, M
    Backes, BJ
    [J]. CHEMISTRY & BIOLOGY, 2001, 8 (12): : 1131 - 1141