Affinity-based target identification for bioactive small molecules

被引:59
作者
Kawatani, Makoto [1 ]
Osada, Hiroyuki [1 ]
机构
[1] RIKEN CSRS, Antibiot Lab, Wako, Saitama 3510198, Japan
关键词
QUANTITATIVE CHEMICAL PROTEOMICS; PROTEIN-LIGAND INTERACTIONS; DRUG DISCOVERY; CANCER-CELLS; HISTONE DEACETYLASE; KINASE INHIBITORS; CAPTURE COMPOUND; TOPOISOMERASE-II; NATURAL-PRODUCTS; MESSENGER-RNA;
D O I
10.1039/c3md00276d
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
Identification of the cellular targets of bioactive small molecules is a crucial step in drug discovery and chemical genetics. Classical affinity purification with small-molecule affinity probes remains the most common approach, but it remains a considerable challenge. To overcome various drawbacks in probe preparation, nonspecific interactions, and the sensitivity of target detection, new methods and techniques are being developed, such as a nonselective universal coupling method based on a photo-affinity reaction, which enables introduction of a variety of small molecules to a solid support without chemical modification to generate small-molecule affinity probes. Here, we review recent progress in affinity-based approaches for small-molecule target identification with a focus on affinity purification.
引用
收藏
页码:277 / 287
页数:11
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