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有核微管的动力学特性:亚临界浓度范围内的GTP利用情况。

Dynamic properties of nucleated microtubules: GTP utilisation in the subcritical concentration regime.

作者信息

Symmons M F, Martin S R, Bayley P M

机构信息

Division of Physical Biochemistry, National Institute for Medical Research, London, UK.

出版信息

J Cell Sci. 1996 Nov;109 ( Pt 11):2755-66. doi: 10.1242/jcs.109.11.2755.

Abstract

Microtubule assembly kinetics have been studied quantitatively under solution conditions supporting microtubule dynamic instability. Purified GTP-tubulin (Tu-GTP) and covalently cross-linked short microtubule seeds (EGS-seeds; Koshland et al. (1988) Nature 331, 499) were used with and without biotinylation. Under sub-critical concentration conditions ([Tu-GTP] < 5.3 microM), significant microtubule growth of limited length was observed on a proportion of the EGS-seeds by immuno-electron microscopy. A sensitive fluorescence assay for microtubule GDP production was developed for parallel assessment of GTP utilisation. This revealed a correlation between the detected microtubule growth and the production of tubulin-GDP, deriving from the shortening phase of the dynamic microtubules. This correlation was confirmed by the action of nocodazole, a specific inhibitor of microtubule assembly, that was found to abolish the GDP release. The variation of the GDP release with tubulin concentration (Jh(c) plot) was determined below the critical concentration (Cc). The GDP production observed was consistent with the elongation of the observed seeded microtubules with an apparent rate constant of 1.5 x 10(6) M-1 second-1 above a threshold of approximately 1 microM tubulin. The form of this Jh(c) plot for elongation below Cc is reproduced by the Lateral Cap model for microtubule dynamic instability adapted for seeded assembly. The behaviour of the system is contrasted with that previously studied in the absence of detectable microtubule elongation (Caplow and Shanks (1990) J. Biol. Chem. 265, 8935-8941). The approach provides a means of monitoring microtubule dynamics at concentrations inaccessible to optical microscopy, and shows that essentially the same dynamic mechanisms apply at all concentrations. Numerical simulation of the subcritical concentration regime shows dynamic growth features applicable to the initiation of microtubule growth in vivo.

摘要

在支持微管动态不稳定性的溶液条件下,对微管组装动力学进行了定量研究。使用了纯化的GTP - 微管蛋白(Tu - GTP)和共价交联的短微管种子(EGS - 种子;Koshland等人,(1988年)《自然》331卷,499页),有生物素化和无生物素化两种情况。在亚临界浓度条件下([Tu - GTP]<5.3微摩尔),通过免疫电子显微镜观察到部分EGS - 种子上有有限长度的显著微管生长。开发了一种用于微管GDP产生的灵敏荧光测定法,用于并行评估GTP利用情况。这揭示了检测到的微管生长与来自动态微管缩短阶段的微管蛋白 - GDP产生之间的相关性。微管组装的特异性抑制剂诺考达唑的作用证实了这种相关性,发现它能消除GDP释放。在临界浓度(Cc)以下测定了GDP释放随微管蛋白浓度的变化(Jh(c)图)。观察到的GDP产生与观察到的接种微管的伸长一致,在微管蛋白浓度约高于1微摩尔的阈值时,表观速率常数为1.5×10⁶ M⁻¹秒⁻¹。适用于接种组装的微管动态不稳定性的侧向帽模型再现了Cc以下伸长的这种Jh(c)图形式。将该系统的行为与先前在没有可检测到的微管伸长情况下研究的行为进行了对比(Caplow和Shanks,(1990年)《生物化学杂志》265卷,8935 - 8941页)。该方法提供了一种在光学显微镜无法达到的浓度下监测微管动力学的手段,并表明基本上相同的动态机制在所有浓度下都适用。亚临界浓度范围的数值模拟显示了适用于体内微管生长起始的动态生长特征。

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