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Temperature sensitivity of vinblastine-induced tubulin polymerization in the presence of microtubule-associated proteins
Authors:Veena Prasad  Mary Ann Jordan and Richard F Ludue?a
Institution:(1) Department of Biochemistry, University of Texas Health Science Center, 78284-7760 San Antonio, Texas;(2) Department of Biological Sciences, The University of California at Santa Barbara, 93106 Santa Barbara, California
Abstract:The antitumor drug vinblastine has been a useful probe for examining the interaction of tubulin with the microtubule-associated proteins (MAPs), specifically with tau and MAP 2. Although tau and MAP 2 can stimulate microtubule assemblyin vitro, their specific interactions with tubulin are known to differ. For example, in the presence of vinblastine, both tau and MAP 2 cause tubulin to form spirals, but tau causes formation of clustered spirals of high turbidity, while MAP 2 causes formation of loose spirals of low turbidity Ludueñaet al., J. Biol. Chem. 259, 12890–12898 (1984)]. Although cold temperatures can inhibit microtubule assembly, cold has no effect on vinblastine-induced tubulin spiral formation. Consequently, we used the vinblastine-tubulin system to examine the interactions of tau and MAP 2 with tubulin at low temperatures. We found that tau-tubulin-vinblastine complexes form about as well at 0°C as at 37°C. In contrast, MAP 2-tubulin-vinblastine complexes form much less well at 0°C than at 37°C. We find, however, that MAP 2, at 0°C, will strongly inhibit, and even reverse, formation of the tau-tubulin-vinblastine complex. This suggests that the temperature-sensitive factor is the MAP 2-stimulated tubulin-tubulin interaction rather than the MAP 2-tubulin interactionper se; this raises the possibility that the tubulin-tubulin interactions stimulated by tau differ in their temperature sensitivity from those stimulated by MAP 2.
Keywords:Vinblastine  tubulin  microtubules  microtubule-associated proteins  tau" target="_blank">gif" alt="tau" align="BASELINE" BORDER="0">
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