Carlier M F, Didry D, Pantaloni D
Laboratoire d'Enzymologie, CNRS, Gif-sur-Yvette, France.
Biochemistry. 1987 Jul 14;26(14):4428-37. doi: 10.1021/bi00388a036.
The tubulin concentration dependence of the rates of microtubule elongation and accompanying GTP hydrolysis has been studied over a large range of tubulin concentration. GTP hydrolysis followed the elongation process closely at low tubulin concentration and became gradually uncoupled at higher concentrations, reaching a limiting rate of 35-40 s-1. The kinetic parameters for microtubule growth were different at low and high tubulin concentrations. Elongation of microtubules has also been studied in solutions containing GDP and GTP in variable proportions. Only traces of GTP present in GDP were necessary to confer a high stability (low critical concentration) to microtubules. Pure GDP-tubulin was found unable to elongate microtubules in the absence of GTP but blocked microtubule ends with an equilibrium dissociation constant of 5-6 microM. These data were accounted for by a model within which, in the presence of GTP-tubulin at high concentration, microtubules grow at a fast rate with a large GTP cap; the GTP cap may be quite short in the region of the critical concentration; microtubule stability is linked to the strong interaction between GTP and GDP subunits at the elongating site; dimeric GDP-tubulin does not have the appropriate conformation to undergo reversible polymerization. These results are discussed with regard to possible role of GDP and GTP and of GTP hydrolysis in microtubule dynamics.
在很大的微管蛋白浓度范围内,研究了微管伸长速率和伴随的GTP水解对微管蛋白浓度的依赖性。在低微管蛋白浓度下,GTP水解与伸长过程紧密相随,而在较高浓度下逐渐解偶联,达到35 - 40 s⁻¹的极限速率。微管生长的动力学参数在低微管蛋白浓度和高微管蛋白浓度下有所不同。还在含有不同比例GDP和GTP的溶液中研究了微管的伸长。GDP中仅存在微量GTP就足以赋予微管高稳定性(低临界浓度)。发现纯GDP - 微管蛋白在没有GTP的情况下无法使微管伸长,但以5 - 6 μM的平衡解离常数封闭微管末端。这些数据由一个模型解释,在该模型中,在高浓度GTP - 微管蛋白存在下,微管以快速速率生长并带有大的GTP帽;在临界浓度区域,GTP帽可能相当短;微管稳定性与伸长位点处GTP和GDP亚基之间的强相互作用有关;二聚体GDP - 微管蛋白没有合适的构象进行可逆聚合。关于GDP、GTP以及GTP水解在微管动力学中的可能作用,对这些结果进行了讨论。