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冲浪、调控与捕获:所有微管尖端追踪蛋白都一样吗?

Surfing, regulating and capturing: are all microtubule-tip-tracking proteins created equal?

作者信息

Vaughan Kevin T

机构信息

Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556, USA.

出版信息

Trends Cell Biol. 2004 Sep;14(9):491-6. doi: 10.1016/j.tcb.2004.07.011.

Abstract

A diverse group of microtubule-binding proteins has been linked through live-cell imaging of green fluorescent protein (GFP) fusion proteins. These proteins share the ability to associate with the plus ends of elongating microtubules and track with these tips as the microtubules grow, in a process known as "tip tracking". Several models have been proposed to explain the significance of this activity, including roles in delivering proteins to the cell periphery and in modulating microtubule dynamics. However, the recent observation that some of the tip trackers colocalize on structures undergoing search-capture suggests that tip tracking could be a fundamental aspect of the search-capture process. Focusing on the shared ability of these proteins to undergo tip tracking, this article is intended to place the search-capture model in the context of other proposed functions and to stimulate discussion in this area.

摘要

通过绿色荧光蛋白(GFP)融合蛋白的活细胞成像,已将多种微管结合蛋白联系起来。这些蛋白具有与延长微管的正端结合并在微管生长时随这些末端移动的能力,这一过程称为“末端追踪”。已经提出了几种模型来解释这种活动的意义,包括在将蛋白质输送到细胞周边以及调节微管动力学方面的作用。然而,最近的观察发现,一些末端追踪蛋白在进行搜索-捕获的结构上共定位,这表明末端追踪可能是搜索-捕获过程的一个基本方面。本文聚焦于这些蛋白进行末端追踪的共同能力,旨在将搜索-捕获模型置于其他提出的功能背景下,并激发该领域的讨论。

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