Click chemistry as a high-throughput amenable platform in catalomics

被引:23
作者
Kalesh, Karunakaran Anandamma [1 ]
Yang, Peng-Yu [1 ,3 ]
Srinivasan, Rajavel [1 ]
Yao, Shao Qin [1 ,2 ,3 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[2] Natl Univ Singapore, Dept Biol Sci, Singapore 117543, Singapore
[3] Natl Univ Singapore, NUS MedChem Program Off Life Sci, Singapore 117543, Singapore
来源
QSAR & COMBINATORIAL SCIENCE | 2007年 / 26卷 / 11-12期
关键词
activity-based probes; catalomics; click chemistry; enzyme inhibitors; fragment-based assembly; inhibitor fingerprinting;
D O I
10.1002/qsar.200740064
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Click chemistry is emerging as a powerful tool to elucidate the complex catalytic functions that enzymes perform in the biological system. Recent advances in proteornics heavily rely on the robust, modular and high-throughput platform offered by click chemistry. This minireview focuses on the central role click chemistry has played on the most recent advances in the chemical proteomic research involving the discovery of enzyme inhibitors and enzyme profiling using Activity-Based Probes (ABPs). The strength and benefit of click chemistry and its novel variants, such as the so-called in situ screening using click chemistry have been even more evident recently when this novel chemistry is coupled with high-throughput assay technologies such as microarrays and characterization techniques such as Liquid Chromatography-Mass Spectrometry in Selected Ion Mode (LCMS-SIM) and multidimensional LC-MS. The invaluable contribution of click chemistry in the emerging field of "Catalomics" is thus firmly established.
引用
收藏
页码:1135 / 1144
页数:10
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