Temperature sensitivity of vinblastine-induced tubulin polymerization in the presence of microtubule-associated proteins |
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Authors: | Veena Prasad Mary Ann Jordan Richard F. Ludue?a |
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Affiliation: | (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 |
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Abstract: | The antitumor drug vinblastine has been a useful probe for examining the interaction of tubulin with the microtubule-associated proteins (MAPs), specifically with and MAP 2. Although 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 and MAP 2 cause tubulin to form spirals, but 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 and MAP 2 with tubulin at low temperatures. We found that -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 -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 differ in their temperature sensitivity from those stimulated by MAP 2. |
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Keywords: | Vinblastine tubulin microtubules microtubule-associated proteins /content/t67k1l16226qx3m6/xxlarge964.gif" alt=" tau" align=" BASELINE" BORDER=" 0" > |
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