Assays for the identification and evaluation of histone acetyltransferase inhibitors

被引:35
作者
Aherne, GW [1 ]
Rowlands, MG [1 ]
Stimson, L [1 ]
Workman, P [1 ]
机构
[1] Inst Canc Res, Canc Res UK Ctr Canc Therapeut, Sutton SM2 5NG, Surrey, England
关键词
histone acetyltransferase; histone deacetylase; gene transcription; chromatin; cancer; high-throughput screening; histone acetyltransferase inhibitors; enzyme-linked immunoassay;
D O I
10.1016/S1046-2023(02)00028-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
There is presently enormous interest in the function and regulatory roles of histone acetyltransferase enzymes. Along with deacetylases it is now evident that these enzymes play a key role in many cellular processes including chromatin remodeling and gene transcription. As such, effective small molecule enzyme inhibitors would be useful tools for molecular pharmacology and may also be suitable for further development into agents for the treatment of diseases such as cancer, A high-throughput assay based on the use of scintillating microplates (FlashPlates) suitable for screening libraries of compounds for inhibitors of acetylase activity is described here. Confirmation of activity of selected compounds is achieved with a conventional filter assay, the details of which are also described. In addition, an assay suitable for confirming that cellular protein acetylation has been altered by inhibition of acetylases or deacetylases is also presented. On the same plate, cells are grown, exposed to compound, fixed, and permeabilized, and protein acetylation is determined using standard ELISA methodology and a europium-labeled second antibody. This latter method provides a medium-throughput alternative to the use of immunoblotting for mechanistic studies. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:245 / 253
页数:9
相关论文
共 71 条
[31]  
Liu L, 1999, MOL CELL BIOL, V19, P1202
[32]  
Mahlknecht U, 2000, MOL CARCINOGEN, V27, P268, DOI 10.1002/(SICI)1098-2744(200004)27:4<268::AID-MC4>3.0.CO
[33]  
2-P
[34]   Structure and function of histone acetyltransferases [J].
Marmorstein, R .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2001, 58 (5-6) :693-703
[35]   Regulation of E2F1 activity by acetylation [J].
Martínez-Balbás, MA ;
Bauer, UM ;
Nielsen, SJ ;
Brehm, A ;
Kouzarides, T .
EMBO JOURNAL, 2000, 19 (04) :662-671
[36]   Histone deacetylase: A target for antiproliferative and antiprotozoal agents [J].
Meinke, PT ;
Liberator, P .
CURRENT MEDICINAL CHEMISTRY, 2001, 8 (02) :211-235
[37]   Transcription - New insights into an old modification [J].
Mizzen, CA ;
Allis, CD .
SCIENCE, 2000, 289 (5488) :2290-2291
[38]  
Mizzen CA, 1999, METHOD ENZYMOL, V304, P675
[39]   DNA TUMOR-VIRUS TRANSFORMING PROTEINS AND THE CELL-CYCLE [J].
MORAN, E .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1993, 3 (01) :63-70
[40]  
Muraoka M, 1996, ONCOGENE, V12, P1565