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This version was published on June 1, 2006
Journal of Biomolecular Screening, Vol. 11, No. 4, 377-389 (2006)
DOI: 10.1177/1087057106286210

Miniaturization and Validation of a Sensitive Multiparametric Cell-Based Assay for the Concomitant Detection of Microtubule-Destabilizing and Microtubule-Stabilizing Agents

Emilie Vassal

Université Joseph Fourier, INSERM U366-CS/DRDC/CEA Grenoble, France

Caroline Barette

CEA, INSERM U366-CS/DRDC/CEA Grenoble, France

Xavier Fonrose

Université Joseph Fourier, INSERM U366-CS/DRDC/CEA Grenoble, France, Université Joseph Fourier, INSERM U366-CS/DRDC/CEA, and Département de Biologie Intégrée, Grenoble, France

Raphaël Dupont

Université Joseph Fourier, Biopuces/DRDC/CEA, Grenoble, France

Emmanuelle Sans-Soleilhac

CEA, INSERM U366-CS/DRDC/CEA Grenoble, France

Laurence Lafanechère

INSERM, U366-CS/DRDC/CEA, Grenoble, France

The authors describe a cell-based assay for anti-microtubule compounds suitable for automation. This assay allows the identification, in a single screening campaign, of both microtubule-destabilizing and microtubule-stabilizing agents. Its rationale is based on the substrate properties of the tubulin-modifying enzymes involved in the tubulin tyrosination cycle. This cycle involves the removal of the C-terminal tyrosine of the tubulin {alpha}-subunit by an ill-defined tubulin carboxypeptidase and its readdition by tubulin tyrosine ligase. Because of the substrate properties of these enzymes, dynamic microtubules, sensitive to depolymerizing drugs, are composed of tyrosinated tubulin, whereas nondynamic, stabilized microtubules are composed of detyrosinated tubulin. Thus depolymerization or stabilization of the microtubule network can easily be detected with double-immunofluorescence staining using antibodies specific to tyrosinated and detyrosinated tubulin. The authors have scaled this assay to the 96-well plate format and adapted its process for an automated handling, including a readout using a microplate reader. They describe the different steps of this adaptation. This assay was validated using known compounds. This new cell-based assay represents an alternative to both global cytotoxicity assays and in vitro tubulin assembly assays commonly used for the detection of microtubule poisons.

Key Words: microtubules • tubulin post-translational modifications • cell-based assay • anticancer drugs • high-content screening


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