Resumen
The antitumor drug vinblastine has been a useful probe for examining the interaction of tubulin with the microtubule-associated proteins (MAPs), specifically with τ and MAP 2. Although τ and MAP 2 can stimulate microtubule assembly in vitro, their specific interactions with tubulin are known to differ. For example, in the presence of vinblastine, both τ and MAP 2 cause tubulin to form spirals, but τ causes formation of clustered spirals of high turbidity, while MAP 2 causes formation of loose spirals of low turbidity [Ludueña et 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 τ and MAP 2 with tubulin at low temperatures. We found that τ-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 τ-tubulin-vinblastine complex. This suggests that the temperature-sensitive factor is the MAP 2-stimulated tubulin-tubulin interaction rather than the MAP 2-tubulin interaction per se; this raises the possibility that the tubulin-tubulin interactions stimulated by τ differ in their temperature sensitivity from those stimulated by MAP 2.
Idioma original | English (US) |
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Páginas (desde-hasta) | 509-515 |
Número de páginas | 7 |
Publicación | Journal of Protein Chemistry |
Volumen | 11 |
N.º | 5 |
DOI | |
Estado | Published - oct 1992 |
Publicado de forma externa | Sí |
ASJC Scopus subject areas
- Biochemistry