Rhizoxin binding to tubulin at the maytansine-binding site

Biochim Biophys Acta. 1987 Dec 7;926(3):215-23. doi: 10.1016/0304-4165(87)90206-6.

Abstract

The binding of rhizoxin, a potent inhibitor of mitosis and in vitro microtubule assembly, to porcine brain tubulin was studied. Tubulin possesses one binding site for rhizoxin per molecule with a dissociation constant (Kd) of 1.7.10(-7) M. Ansamitocin P-3, a homologue of maytansine, was a competitive inhibitor of rhizoxin binding, with an inhibition constant of 1.3.10(-7) M. Vinblastine also inhibited rhizoxin binding, but was not fully competitive, and the inhibition constant was 2.9.10(-6) M. In contrast, both rhizoxin and ansamitocin P-3 were potent inhibitors of vinblastine binding. Rhizoxin inhibited tau-promoted tubulin assembly, but it, differing from vinblastine, did not induce tubulin aggregation into spirals, even at a concentration as high as 2.10(-5) M. In addition, rhizoxin strongly inhibited vinblastine-induced tau-dependent tubulin aggregation. Rhizoxin binding to tubulin was completely independent from colchicine binding. These effects resemble those of maytansine. The results suggested that rhizoxin binds to the maytansine-binding site and that the binding sites of rhizoxin and vinblastine are not the same.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Binding, Competitive
  • Colchicine / pharmacology
  • Kinetics
  • Lactones / metabolism
  • Macrolides
  • Maytansine / analogs & derivatives
  • Maytansine / metabolism*
  • Microscopy, Electron
  • Microtubule-Associated Proteins / metabolism
  • Microtubules / ultrastructure
  • Oxazines / metabolism*
  • Swine
  • Tubulin / metabolism*
  • Vinblastine / pharmacology
  • tau Proteins

Substances

  • Lactones
  • Macrolides
  • Microtubule-Associated Proteins
  • Oxazines
  • Tubulin
  • tau Proteins
  • Maytansine
  • Vinblastine
  • ansamitocins
  • rhizoxin
  • Colchicine