Caplow M, Shanks J
Department of Biochemistry, University of North Carolina, Chapel Hill 27599-7260, USA.
Biochemistry. 1998 Sep 15;37(37):12994-3002. doi: 10.1021/bi972602+.
The proposal that microtubule dynamic instability results from stabilization of microtubule ends by tubulin-GDP-Pi subunits (where Pi is inorganic phosphate) [Melki et al. (1996) Biochemistry 35, 12038] was based on studies of GTP hydrolysis and microtubule assembly that showed that tubulin-GDP-Pi subunits can transiently accumulate at microtubule ends. There is no direct evidence that GDP-Pi-subunits can stabilize microtubules under conditions where dynamic instability is observed and this has been inferred from the observation that tubulin-GDP-BeFn subunits stabilize microtubules. To test if tubulin-GDP-Pi stabilizes microtubules we sought evidence for a synergism between the effect of Pi and BeFn. We found, however, that Pi antagonizes the effect of BeFn by displacing it from tubulin subunits. The alternate mechanism in which Pi inhibits BeFn stabilization of microtubules by displacing fluoride from beryllium was ruled out from the 9Be and 19F NMR spectra in the presence and absence of Pi. Further evidence that tubulin-GDP-BeFn is not an analogue of tubulin-GDP-Pi and that tubulin-GDP-Pi is not responsible for maintaining the growth phase in microtubules manifesting dynamic instability was provided by our observation that Pi did not decrease the disassembly rate under conditions where tubulin-GDP-Pi subunits are expected to have formed. Results showing that BeFn binds randomly to subunits in microtubules provided evidence that Pi dissociation from the tubulin-GDP-Pi intermediate formed during GTP hydrolysis occurs randomly rather than processively starting at the growing microtubule tip.
微管动态不稳定性是由微管蛋白 - GDP - Pi亚基(其中Pi是无机磷酸)稳定微管末端所致的这一观点[梅尔基等人(1996年)《生物化学》35卷,12038页]是基于对GTP水解和微管组装的研究得出的,这些研究表明微管蛋白 - GDP - Pi亚基能够在微管末端短暂积累。没有直接证据表明GDP - Pi亚基在观察到动态不稳定性的条件下能够稳定微管,这是从微管蛋白 - GDP - BeFn亚基能稳定微管的观察结果推断出来的。为了测试微管蛋白 - GDP - Pi是否能稳定微管,我们寻找了Pi和BeFn效应之间协同作用的证据。然而,我们发现Pi通过从微管蛋白亚基上取代BeFn来拮抗其效应。在有和没有Pi的情况下,通过9Be和19F NMR光谱排除了Pi通过从铍上取代氟来抑制微管蛋白 - BeFn对微管稳定作用的另一种机制。我们观察到在预期微管蛋白 - GDP - Pi亚基已形成的条件下Pi并没有降低解聚速率,这进一步证明了微管蛋白 - GDP - BeFn不是微管蛋白 - GDP - Pi的类似物,且微管蛋白 - GDP - Pi并不负责维持表现出动态不稳定性的微管中的生长阶段。结果表明BeFn随机结合到微管中的亚基上,这提供了证据,表明在GTP水解过程中形成的微管蛋白 - GDP - Pi中间体上的Pi解离是随机发生的,而不是从生长的微管尖端开始逐步进行的。