Sternlicht H, Ringel I
J Biol Chem. 1979 Oct 25;254(20):10540-50.
Colchicine.tubulin complex (CD) inhibits microtubule assembly. We examined this inhibition under conditions where spontaneous nucleation was suppressed and assembly was restricted to an elongation polymerization. We found that CD inhibited assembly by a mechanism which preserved the ability of microtubule ends to add tubulin. This observation is inconsistent with the end-poisoning model which recently was proposed as a general mechanism for assembly inhibition by CD. Our data are consistent with the following model: (a) microtubules formed in the presence of CD are CD-tubulin copolymers; (b) these copolymers can have appreciable numbers of incorporated CDs which are, most likely, randomly distributed in the copolymers; (c) CD-tubulin copolymers have assembly-competent ends with association and dissociation rate constants which decrease as the CD/tubulin ratio in the copolymers, (CD/T)MT, increases; and (d) the critical tubulin concentrations required for microtubule assembly increase in the presence of CD, indicating that copolymer affinity for tubulin decreases as (CD/T)MT increases.
秋水仙碱 - 微管蛋白复合物(CD)抑制微管组装。我们在自发成核受到抑制且组装仅限于伸长聚合的条件下研究了这种抑制作用。我们发现,CD通过一种保留微管末端添加微管蛋白能力的机制来抑制组装。这一观察结果与最近提出的作为CD抑制组装的一般机制的末端中毒模型不一致。我们的数据与以下模型一致:(a)在CD存在下形成的微管是CD - 微管蛋白共聚物;(b)这些共聚物可以含有相当数量的掺入的CD,这些CD很可能随机分布在共聚物中;(c)CD - 微管蛋白共聚物具有组装能力的末端,其缔合和解离速率常数随着共聚物中CD/微管蛋白比例((CD/T)MT)的增加而降低;(d)在CD存在下微管组装所需的临界微管蛋白浓度增加,表明共聚物对微管蛋白的亲和力随着(CD/T)MT的增加而降低。