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
  • [31] Winssinger N, 2001, ANGEW CHEM INT EDIT, V40, P3152, DOI 10.1002/1521-3773(20010903)40:17<3152::AID-ANIE3152>3.0.CO
  • [32] 2-P
  • [33] Target protease specificity of the viral serpin CrmA - Analysis of five caspases
    Zhou, Q
    Snipas, S
    Orth, K
    Muzio, M
    Dixit, VM
    Salvesen, GS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (12) : 7797 - 7800