maytansine and 5-5--bis(8-(phenylamino)-1-naphthalenesulfonate)

maytansine has been researched along with 5-5--bis(8-(phenylamino)-1-naphthalenesulfonate)* in 1 studies

Other Studies

1 other study(ies) available for maytansine and 5-5--bis(8-(phenylamino)-1-naphthalenesulfonate)

ArticleYear
The interaction of phomopsin A with bovine brain tubulin.
    Archives of biochemistry and biophysics, 1989, Volume: 272, Issue:1

    Phomopsin A is an anti-mitotic compound from the fungus Phomopsis leptostroniformis which is a potent inhibitor of microtubule assembly in vitro; like maytansine, it is known to compete with vinblastine for binding to tubulin (E. Lacey, J. A. Edgar, and C. C. J. Culvenor (1987) Biochem. Pharmacol. 36, 2133-2138). A major difference between the effects of maytansine and vinblastine is that vinblastine is a potent inhibitor of tubulin decay, whereas maytansine has little or no effect on decay. Since phomopsin A is structurally distinct from either maytansine or vinblastine, tubulin decay may be measured by either the time-dependent loss of the ability to bind to [3H]colchicine or the time-dependent increase in the binding of bis(8-anilinonaphthalene 1-sulfonate) (BisANS) to tubulin. By either method, phomopsin A was found to be a much stronger inhibitor of tubulin decay than is vinblastine or any other drug yet tested, and in fact, when decay is measured by the increase of BisANS binding, phomopsin A appears to stop the process entirely. This may prove to be useful in the determination of the higher-order structure of the tubulin molecule.

    Topics: Anilino Naphthalenesulfonates; Animals; Brain Chemistry; Cattle; Colchicine; Fluorescent Dyes; Kinetics; Maytansine; Molecular Structure; Mycotoxins; Spectrometry, Fluorescence; Tubulin; Vinblastine

1989