Solid-Phase Biological Assays for Drug Discovery

被引:11
作者
Forsberg, Erica M. [1 ]
Sicard, Clemence [1 ]
Brennan, John D. [1 ]
机构
[1] McMaster Univ, Biointerfaces Inst, Hamilton, ON L8S 4L8, Canada
来源
ANNUAL REVIEW OF ANALYTICAL CHEMISTRY, VOL 7 | 2014年 / 7卷
关键词
bioaffinity chromatography; protein microarrays; membrane proteins; kinases; FRONTAL AFFINITY-CHROMATOGRAPHY; NICOTINIC ACETYLCHOLINE-RECEPTOR; TANDEM MASS-SPECTROMETRY; ENZYME-CATALYZED REACTIONS; LIGAND-BINDING DOMAIN; HUMAN SERUM-ALBUMIN; HIGH-THROUGHPUT; LIQUID-CHROMATOGRAPHY; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; NONCOMPETITIVE INHIBITORS;
D O I
10.1146/annurev-anchem-071213-020241
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the past 30 years, there has been a significant growth in the use of solid-phase assays in the area of drug discovery, with a range of new assays being used for both soluble and membrane-bound targets. In this review, we provide some basic background to typical drug targets and immobilization protocols used in solid-phase biological assays (SPBAs) for drug discovery, with emphasis on particularly labile biomolecular targets such as kinases and membrane-bound receptors, and highlight some of the more recent approaches for producing protein microarrays, bioaffinity columns, and other devices that are central to small molecule screening by SPBA. We then discuss key applications of such assays to identify drug leads, with an emphasis on the screening of mixtures. We conclude by highlighting specific advantages and potential disadvantages of SPBAs, particularly as they relate to particular assay formats.
引用
收藏
页码:337 / 359
页数:23
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