Caplow M, Shanks J, Brylawski B P
J Biol Chem. 1985 Oct 15;260(23):12675-9.
We have demonstrated that tubulin-GTP subunits can react with microtubule ends containing subunits with E-site-bound GDP. This observation can be taken to rule out a previous interpretation of a biphasic dependence of the rate for subunit flux into microtubules on the subunit concentration, which is based upon an assumption that GTP is required to be present in subunits at microtubule ends in order to allow addition of tubulin-GTP subunits. The nullified mechanism had been suggested to be the basis of the observation that growing and shrinking microtubules coexist as independent species. We have also confirmed previous studies indicating that the flux rate is nonlinearly dependent on the subunit concentration and account for this behavior by assuming that tubulin-GTP subunits reversibly add to microtubule ends by two paths. In one, tubulin-GTP subunits add nonproductively to generate an end which is unable to undergo further net microtubule elongation; however, this reaction can retard the rate for microtubule disassembly under conditions where the disassembly reaction predominates. In the other, tubulin-GTP subunits add productively to microtubule ends to generate ends which can undergo subsequent net elongation.
我们已经证明,微管蛋白-GTP亚基可以与含有E位点结合GDP的亚基的微管末端发生反应。这一观察结果可以排除之前对亚基流入微管的速率对亚基浓度呈双相依赖性的一种解释,该解释基于这样一种假设,即微管末端的亚基中需要存在GTP,以便允许添加微管蛋白-GTP亚基。已被否定的机制曾被认为是生长和收缩的微管作为独立物种共存这一观察结果的基础。我们还证实了先前的研究,即通量速率非线性地依赖于亚基浓度,并通过假设微管蛋白-GTP亚基通过两条途径可逆地添加到微管末端来解释这种行为。在一种途径中,微管蛋白-GTP亚基非生产性地添加,产生一个无法进行进一步净微管伸长的末端;然而,在解聚反应占主导的条件下,这种反应可以减缓微管解聚的速率。在另一种途径中,微管蛋白-GTP亚基生产性地添加到微管末端,产生可以进行后续净伸长的末端。