Pirollet F, Job D, Margolis R L, Garel J R
INSERM U244, Département de Recherche Fondamentale, Grenoble, France.
EMBO J. 1987 Nov;6(11):3247-52. doi: 10.1002/j.1460-2075.1987.tb02642.x.
Depending upon the conditions under which polymerization takes place, pure tubulin can assemble into microtubules following either the usual monotonic kinetics or a more complex oscillatory mechanism. When present, these oscillations involve large cyclic changes in the extent of polymer formed before a steady-state is reached. Analysis of the microtubules formed at different times shows that these oscillations involve marked redistribution in both the length and number of microtubules. No significant difference is found between two populations of microtubules corresponding to the same level of assembly, one for which the extent of polymerization will remain stable with time and one for which it will decrease by as much as 90% in the next oscillation. The amplitude of these oscillations is sensitive to changes in the concentrations of protein, nucleotide (GTP, GDP or GMPpNp), magnesium ion or GTP regenerating system. A complete shift from an oscillatory to a monotonic polymerization can be induced by a minor increase in the concentration of free nucleotide, GTP or GDP.
根据聚合反应发生的条件,纯微管蛋白可以按照通常的单调动力学或更复杂的振荡机制组装成微管。当存在这些振荡时,在达到稳态之前,聚合物形成的程度会发生大幅度的周期性变化。对不同时间形成的微管进行分析表明,这些振荡涉及微管长度和数量的显著重新分布。在对应于相同组装水平的两组微管之间未发现显著差异,一组微管的聚合程度随时间保持稳定,另一组微管的聚合程度在下一次振荡中会下降多达90%。这些振荡的幅度对蛋白质浓度、核苷酸(GTP、GDP或GMPpNp)、镁离子或GTP再生系统的变化敏感。游离核苷酸GTP或GDP浓度的微小增加可导致从振荡聚合到单调聚合的完全转变。