Evaluation of the tubulin-bound paclitaxel conformation:: Synthesis, biology, and SAR studies of C-4 to C-3′ bridged paclitaxel analogues

被引:59
作者
Ganesh, Thota
Yang, Chao
Norris, Andrew
Glass, Tom
Bane, Susan
Ravindra, Rudravajhala
Banerjee, Abhijit
Metaferia, Belhu
Thomas, Shala L.
Giannakakou, Paraskevi
Alcaraz, Ana A.
Lakdawala, Ami S.
Snyder, James P.
Kingston, David G. I. [1 ]
机构
[1] SUNY Binghamton, Dept Chem, Binghamton, NY 13902 USA
[2] Virginia Polytech Inst & State Univ, Dept Chem, Blacksburg, VA 24061 USA
[3] Emory Univ, Dept Chem, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Winship Canc Inst, Atlanta, GA 30322 USA
关键词
D O I
10.1021/jm061071x
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The important anticancer drug paclitaxel binds to the beta-subunit of the alpha beta-tubulin dimer in the microtubule in a stoichiometric ratio, promoting microtubule polymerization and stability. The conformation of microtubule-bound drug has been the subject of intense study, and various suggestions have been proposed. In previous work we presented experimental and theoretical evidence that paclitaxel adopts a T-shaped conformation when it is bound to tubulin. In this study we report additional experimental data and calculations that delineate the allowable parameters for effective paclitaxel-tubulin interactions.
引用
收藏
页码:713 / 725
页数:13
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