A pipeline for ligand discovery using small-molecule microarrays

被引:73
作者
Duffner, Jay L.
Clemons, Paul A.
Koehler, Angela N.
机构
[1] Harvard Univ, Broad Inst, Cambridge, MA 02142 USA
[2] MIT, Cambridge, MA 02142 USA
关键词
D O I
10.1016/j.cbpa.2006.11.031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Uncovering the functions of thousands of gene products, in various states of post-translational modification, is a key challenge in the post-genome era. To identify small-molecule probes for each protein function, high-throughput methods for ligand discovery are needed. In recent years, small-molecule microarrays (SMMs) have emerged as high-throughput and miniaturized screening tools for discovering protein-small-molecule interactions. Microarrays of small molecules from a variety of sources, including FDA-approved drugs, natural products and products of combinatorial chemistry and diversity-oriented synthesis, have been prepared and screened by several laboratories, leading to several newly discovered protein-ligand pairs.
引用
收藏
页码:74 / 82
页数:9
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