Voter W A, Erickson H P
J Biol Chem. 1984 Aug 25;259(16):10430-8.
A model describing the nucleation and assembly of purified tubulin has been developed. The novel feature of this model is a two stage nucleation process to allow the explicit inclusion of the two-dimensional nature of the early stages of microtubule assembly. In actin assembly the small starting nucleus has only one site for subunit addition as the two-stranded helix is formed. In contrast, microtubule assembly begins with the formation of a small two-dimensional section of microtubule wall. The model we propose is a modification of the work of Wegner and Engel (Wegner, A., and Engel, J. (1975) Biophys. Chem. 3, 215-225) wherein we add a second stage of nucleation to directly account for lateral growth, i.e. the addition of a small number of subunits to the side of an existing sheet structure. Subsequent elongation of the sheets is treated in the usual way. The experimental system used to test this model was the Mg2+/glycerol induced assembly of purified tubulin. The computer simulation of the polymerization time courses gave a fairly good fit to experimental kinetics for our model, where the primary nucleus comprises two protofilaments, of four and three subunits, and lateral growth requires a three-subunit nucleus to initiate a new protofilament.
已开发出一种描述纯化微管蛋白成核与组装的模型。该模型的新颖之处在于其两阶段成核过程,以便明确纳入微管组装早期阶段的二维特性。在肌动蛋白组装过程中,由于形成了双链螺旋,小的起始核只有一个亚基添加位点。相比之下,微管组装始于微管壁小二维部分的形成。我们提出的模型是对韦格纳和恩格尔(Wegner, A., and Engel, J. (1975) Biophys. Chem. 3, 215 - 225)工作的改进,其中我们增加了第二阶段成核,以直接解释横向生长,即在现有片状结构的一侧添加少量亚基。随后片层的伸长以常规方式处理。用于测试该模型的实验系统是Mg2 + /甘油诱导的纯化微管蛋白组装。对于我们的模型,聚合时间进程的计算机模拟与实验动力学相当吻合,其中初级核由两条原丝组成,分别有四个和三个亚基,横向生长需要一个三个亚基的核来启动一条新的原丝。