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A fluorescence-based high-throughput assay for antimicrotubule drugs

  • Donna M. Barron
  • , Sabarni K. Chatterjee
  • , Rudravajhala Ravindra
  • , Rebecca Roof
  • , Erkan Baloglu
  • , David G.I. Kingston
  • , Susan Bane
  • State University of New York Binghamton University
  • Regeneron Pharmaceuticals, Inc.
  • Virginia Polytechnic Institute and State University

Research output: Contribution to journalArticlepeer-review

73 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)49-56
Number of pages8
JournalAnalytical Biochemistry
Volume315
Issue number1
DOIs
StatePublished - Apr 1 2003

Keywords

  • Antimitotic
  • Colchicine
  • DAPI
  • High-throughput assay
  • Microtubule
  • Polymerization
  • Taxol
  • Tubulin

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