| Literature DB >> 18588888 |
Francois Devred1, Philipp O Tsvetkov, Pascale Barbier, Diane Allegro, Susan Band Horwitz, Alexander A Makarov, Vincent Peyrot.
Abstract
Microtubule (MT) dynamic instability is tightly regulated by stabilizing and destabilizing proteins, the latter being exemplified by stathmin/Op18, a protein known to destabilize MTs. Studies in cells have indicated that the level of stathmin expression modifies the cytotoxicity of antimicrotubule drugs, such as vinblastine (VLB). Using isothermal titration calorimetry and analytical ultracentrifugation, we show that VLB increases the affinity of stathmin for tubulin 50-fold (and vice versa). These results are the first biochemical evidence of the direct relationship between stathmin and an antimitotic drug, and reveal a new mechanism of action for VLB.Entities:
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Year: 2008 PMID: 18588888 PMCID: PMC2837597 DOI: 10.1016/j.febslet.2008.06.035
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124