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Miniaturization and Validation of a Sensitive Multiparametric Cell-Based Assay for the Concomitant Detection of Microtubule-Destabilizing and Microtubule-Stabilizing AgentsUniversité Joseph Fourier, INSERM U366-CS/DRDC/CEA Grenoble, France
CEA, INSERM U366-CS/DRDC/CEA Grenoble, France
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
Université Joseph Fourier, Biopuces/DRDC/CEA, Grenoble, France
CEA, INSERM U366-CS/DRDC/CEA Grenoble, France
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
Key Words: microtubules tubulin post-translational modifications cell-based assay anticancer drugs high-content screening
This version was published on June
1, 2006 Journal of Biomolecular Screening, Vol. 11, No. 4,
377-389 (2006) This article has been cited by other articles:
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-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. 
