A fluorescence-based high-throughput assay for antimicrotubule drugs

被引:72
作者
Barron, DM
Chatterjee, SK
Ravindra, R
Roof, R
Baloglu, E
Kingston, DGI
Bane, S [1 ]
机构
[1] SUNY Binghamton, Dept Chem, Binghamton, NY 13902 USA
[2] Virginia Polytech Inst & State Univ, Dept Chem, Blacksburg, VA 24061 USA
关键词
tubulin; microtubule; taxol; colchicine; DAPI; polymerization; high-throughput assay; antimitotic;
D O I
10.1016/S0003-2697(02)00691-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
With the advent of combinatorial chemistry and the extensive libraries of potential drugs produced from it, there is a growing need for rapid sensitive, high-throughput screening for drug potency. Microtubules are important targets for anticancer agents, and new antimicrotubule compounds are of continued interest in drug development. The in vitro potency of antimicrotubule drugs may be evaluated by measuring the extent of tubulin assembly. The extent of polymerization is proportional to the turbidity of the solution, which usually has been measured as apparent absorption. The turbidity method has inherent problems that hinder its adaptation to a high-throughput format, such as a requirement for high protein concentrations and a high coefficient of variation. We present here a high-throughput assay for antimicrotubule activity in which fluorescence is used to monitor microtubule assembly. Both assembly-inhibiting and assembly-promoting compounds can be evaluated. The assay is rapid and easy to perform, and the data are reliable, with good accuracy and reproducibility. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:49 / 56
页数:8
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