Development of an ELISA-Based HDAC Activity Assay for Characterization of Isoform-Selective Inhibitors

被引:19
|
作者
Padige, Geetha [1 ]
Negmeldin, Ahmed T. [1 ]
Pflum, Mary Kay H. [1 ]
机构
[1] Wayne State Univ, Dept Chem, Detroit, MI 48202 USA
基金
美国国家卫生研究院;
关键词
cancer; histone deacetylases (HDAC); isoform selective HDAC inhibitors; enzyme-linked immunosorbent assay; HISTONE DEACETYLASE INHIBITORS; SCREENING ASSAYS; GASTRIC-CANCER; EXPRESSION; ACETYLATION; VALIDATION; PHASE-1; DESIGN;
D O I
10.1177/1087057115598118
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Histone deacetylase (HDAC) proteins are promising targets for cancer treatment, with several HDAC inhibitors used clinically as anticancer drugs. Most HDAC inhibitors nonspecifically interact with all or many of the 11 HDAC isoforms. Isoform-selective HDAC inhibitors would be useful tools to dissect the individual functions of HDAC proteins in cancer formation, in addition to potentially displaying effective anticancer properties. We report here a robust HDAC activity assay for screening selective HDAC inhibitors, which is inspired by the traditional enzyme-linked immunosorbent assay (ELISA). The key feature of the ELISA-based HDAC activity assay is use of mammalian cell-derived HDAC isoforms instead of recombinant proteins. Importantly, the assay was validated with several known HDAC inhibitors. The ELISA-based HDAC activity assay will facilitate the characterization of isoform-selective HDAC inhibitors against mammalian cell-derived HDAC proteins, which will enhance HDAC-centered cancer research and provide a foundation for anticancer drug development.
引用
收藏
页码:1277 / 1285
页数:9
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