Karr T L, Podrasky A E, Purich D L
Proc Natl Acad Sci U S A. 1979 Nov;76(11):5475-9. doi: 10.1073/pnas.76.11.5475.
Critical concentrations for formation of microtubules from subunits with GTP and its beta, gamma-imido and beta, gamma-methylene analogs are similar when adequate time is given for equilibration. Dilution of microtubules into GTP and GDP yielded values of 0.1 and 0.19 mg/ml for the critical concentration, results similar to those reported by Carlier and Pantaloni [Carlier, M. & Pantaloni, D. (1978) Biochemistry 17, 1908-1915]. GDP is capable of supporting elongation of preformed microtubules, but it efficiently poisons the nucleation events. Reported experiments also demonstrate that the critical tubulin concentration of the tubulin-GDP complex can be accurately measured in both the assembly and disassembly directions. Evidence is presented that GTP is involved in early nucleation events but that microtubules are stabilized in the presence of either GTP or GDP. These results are discussed in terms of a condensation-equilibrium model in which tubulin subunits equilibrate rapidly with microtubule ends, and their affinity for the ends is governed by the nucleotide ligand at the exchangeable site.
如果给予足够时间进行平衡,由带有鸟苷三磷酸(GTP)及其β,γ-亚氨基和β,γ-亚甲基类似物的亚基形成微管的临界浓度是相似的。将微管稀释到GTP和鸟苷二磷酸(GDP)中,得到的临界浓度值分别为0.1和0.19毫克/毫升,这一结果与卡利尔(Carlier)和潘塔洛尼(Pantaloni)报道的结果相似[卡利尔,M. & 潘塔洛尼,D.(1978年)《生物化学》17卷,1908 - 1915页]。GDP能够支持预先形成的微管的延长,但它会有效地抑制成核事件。已报道的实验还表明,在组装和解聚方向上都可以准确测量微管蛋白 - GDP复合物的临界微管蛋白浓度。有证据表明,GTP参与早期成核事件,但微管在GTP或GDP存在的情况下都会稳定下来。这些结果将根据一个凝聚 - 平衡模型进行讨论,在该模型中,微管蛋白亚基与微管末端快速平衡,并且它们对末端的亲和力由可交换位点处的核苷酸配体决定。