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Volume 271,
Number 11,
Issue of March 15, 1996 pp. 6192-6198
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
Mechanism
of Action of Cryptophycin
INTERACTION WITH THE Vinca ALKALOID DOMAIN OF TUBULIN
(Received for publication, August 23, 1995; and in revised form, January 3, 1996)
Charles D.
Smith ,
Xinqun
Zhang
Cryptophycin is a potent antitumor agent that depletes
microtubules in intact cells, including cells with the multidrug
resistance phenotype. To determine the mechanism of action of
cryptophycin, its effects on tubulin function in vitro were
analyzed. Cryptophycin reduced the in vitro polymerization of
bovine brain microtubules by 50% at a drug:tubulin ratio of 0.1.
Cryptophycin did not alter the critical concentration of tubulin
required for polymerization, but instead caused substoichiometric
reductions in the amount of tubulin that was competent for assembly.
Consistent with its persistent effects on intact cells,
cryptophycin-treated microtubule protein remained
polymerization-defective even after cryptophycin was reduced to
sub-inhibitory concentrations. The effects of cryptophycin were not due
to denaturation of tubulin and were associated with the accumulation of
rings of microtubule protein. The site of cryptophycin interaction
with tubulin was examined using functional and competitive binding
assays. Cryptophycin blocked the formation of vinblastine-tubulin
paracrystals in intact cells and suppressed vinblastine-induced tubulin
aggregation in vitro. Cryptophycin inhibited the binding of
[ H]vinblastine and the hydrolysis of
[ - P]GTP by isolated tubulin, but did not
block the binding of colchicine. These results indicate that
cryptophycin disrupts the Vinca alkaloid site of tubulin;
however, the molecular details of this interaction are distinct from
those of other antimitotic drugs.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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