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稳定微管所需的最小GTP帽。

The minimum GTP cap required to stabilize microtubules.

作者信息

Drechsel D N, Kirschner M W

机构信息

Department of Biochemistry and Biophysics, University of California, San Francisco 94143-0448, USA.

出版信息

Curr Biol. 1994 Dec 1;4(12):1053-61. doi: 10.1016/s0960-9822(00)00243-8.

Abstract

BACKGROUND

Microtubules polymerized from pure tubulin show the unusual property of dynamic instability, in which both growing and shrinking polymers coexist at steady state. Shortly after its addition to a microtubule end, a tubulin subunit hydrolyzes its bound GTP. Studies with non-hydrolyzable analogs have shown that GTP hydrolysis is not required for microtubule assembly, but is essential for generating a dynamic polymer, in which the subunits at the growing tip have bound GTP and those in the bulk of the polymer have bound GDP. It has been suggested that loss of the 'GTP cap' through dissociation or hydrolysis exposes the unstable GDP core, leading to rapid depolymerization. However, evidence for a stabilizing cap has been very difficult to obtain.

RESULTS

We developed an assay to determine the minimum GTP cap necessary to stabilize a microtubule from shrinking. Assembly of a small number of subunits containing a slowly hydrolyzed GTP analog (GMPCPP) onto the end of dynamic microtubules stabilized the polymer to dilution. By labeling the subunits with rhodamine, we measured the size of the cap and found that as few as 40 subunits were sufficient to stabilize a microtubule.

CONCLUSIONS

On the basis of statistical arguments, in which the proportion of stabilized microtubules is compared to the probability that when 40 GMPCPP-tubulin subunits have polymerized onto a microtubule end, all protofilaments have added at least one GMPCPP-tubulin subunit, our measurements of cap size support a model in which a single GTP subunit at the end of each of the 13 protofilaments of a microtubule is sufficient for stabilization. Depolymerization of a microtubule may be initiated by an exposed tubulin-GDP subunit at even a single position. These results have implications for the structure of microtubules and their means of regulation.

摘要

背景

由纯微管蛋白聚合而成的微管展现出动态不稳定性这一不同寻常的特性,即在稳态下生长和收缩的聚合物共存。微管蛋白亚基添加到微管末端后不久,就会水解其结合的GTP。对不可水解类似物的研究表明,GTP水解对于微管组装并非必需,但对于生成动态聚合物至关重要,在这种聚合物中,生长末端的亚基结合有GTP,而聚合物主体中的亚基结合有GDP。有人提出,通过解离或水解导致“GTP帽”的丢失会暴露出不稳定的GDP核心,从而导致快速解聚。然而,很难获得关于稳定帽的证据。

结果

我们开发了一种测定方法,以确定稳定微管使其不收缩所需的最小GTP帽。将少量含有缓慢水解的GTP类似物(GMPCPP)的亚基组装到动态微管末端,可使聚合物在稀释时保持稳定。通过用罗丹明标记亚基,我们测量了帽的大小,发现少至40个亚基就足以稳定微管。

结论

基于统计学观点,即将稳定微管的比例与当40个GMPCPP - 微管蛋白亚基聚合到微管末端时所有原纤维都添加了至少一个GMPCPP - 微管蛋白亚基的概率进行比较,我们对帽大小的测量支持了这样一种模型,即微管的13条原纤维每条末端的单个GTP亚基就足以实现稳定。即使在单个位置暴露的微管蛋白 - GDP亚基也可能引发微管的解聚。这些结果对微管的结构及其调节方式具有启示意义。

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