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微管相关蛋白(MAPs)的微管稳定活性源于动态不稳定性中拯救频率的增加:随着MAPs与微管结合,缩短长度会减少。

Microtubule-stabilizing activity of microtubule-associated proteins (MAPs) is due to increase in frequency of rescue in dynamic instability: shortening length decreases with binding of MAPs onto microtubules.

作者信息

Itoh T J, Hotani H

机构信息

Department of Molecular Biology, School of Science, Nagoya University, Japan.

出版信息

Cell Struct Funct. 1994 Oct;19(5):279-90. doi: 10.1247/csf.19.279.

DOI:10.1247/csf.19.279
PMID:7850890
Abstract

The role of microtubule associated proteins (MAPs) on the dynamic instability of microtubules was examined under a dark-field microscope using bovine brain tubulin purified by DEAE-Sepharose column chromatography. In the absence of MAPs, the transition from the shortening phase to the growing phase (the rescue) occurred rarely both in self-assembled microtubules and seeded ones, especially at the plus end. Even under the conditions unfavorable to stabilize microtubule, the addition of a small amount of crude MAPs or purified microtubule associated protein 2 (MAPs) to the microtubules allowed them to undergo the rescue. At increased concentrations of MAPs or MAP2, both the length change required for a rescue during shortening phase ("shortening length") and for a catastrophe (transition from the growing to the shortening phase) ("growth length") decreased. Under these conditions, the rescue often occurred at the same site where previous rescues occurred. Distribution of immunofluorescent MAP2 antibodies along individual microtubules showed that MAP2 molecules bound onto microtubules by forming discrete clusters. The number of MAP2 molecules per cluster was estimated to be between 25 and 60. Because both the "shortening length" and the distance between MAP2 clusters in a microtubule decreased with increased MAPs concentration, we suggest that the MAP2 clusters may form the specific site at which the shortening of the microtubule readily stops. MAP2 possibly regulates the dynamic instability by stopping the shortening, which is a prerequisite for the rescue.

摘要

利用经DEAE - 琼脂糖柱层析纯化的牛脑微管蛋白,在暗视野显微镜下研究了微管相关蛋白(MAPs)对微管动态不稳定性的作用。在没有MAPs的情况下,自组装微管和接种微管中从缩短阶段到生长阶段的转变(救援)很少发生,尤其是在正端。即使在不利于稳定微管的条件下,向微管中添加少量粗制MAPs或纯化的微管相关蛋白2(MAP2)也能使它们发生救援。在MAPs或MAP2浓度增加时,缩短阶段救援所需的长度变化(“缩短长度”)和灾难(从生长阶段到缩短阶段的转变)所需的长度变化(“生长长度”)均降低。在这些条件下,救援经常发生在先前救援发生的同一位置。沿单个微管的免疫荧光MAP2抗体分布表明,MAP2分子通过形成离散簇与微管结合。每个簇中MAP2分子的数量估计在25到60之间。由于微管中“缩短长度”和MAP2簇之间的距离都随着MAPs浓度的增加而减小,我们认为MAP2簇可能形成了微管缩短容易停止的特定位点。MAP2可能通过阻止缩短来调节动态不稳定性,而缩短的停止是救援的前提条件。

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Microtubule-stabilizing activity of microtubule-associated proteins (MAPs) is due to increase in frequency of rescue in dynamic instability: shortening length decreases with binding of MAPs onto microtubules.微管相关蛋白(MAPs)的微管稳定活性源于动态不稳定性中拯救频率的增加:随着MAPs与微管结合,缩短长度会减少。
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