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微管结合蛋白的扩散相互作用。

The diffusive interaction of microtubule binding proteins.

作者信息

Cooper Jeremy R, Wordeman Linda

机构信息

Department of Physiology and Biophysics, University of Washington School of Medicine, Seattle, WA 98195, USA.

出版信息

Curr Opin Cell Biol. 2009 Feb;21(1):68-73. doi: 10.1016/j.ceb.2009.01.005. Epub 2009 Jan 29.

Abstract

Microtubule-based motility is often thought of as specifically referring to the directed stepping of microtubule-based motors such as kinesin or dynein. However, microtubule lattice diffusion (also known as diffusional motility) provides a second mode of transport that is shared by a much broader class of microtubule binding proteins. Microtubule lattice diffusion offers distinct advantages as a transport mechanism including speed, bidirectional microtubule end targeting, and no requirement for direct chemical energy (i.e. ATP). It remains to be seen whether a universal binding mechanism for this interaction will be identified but electrostatic interactions appear to play a significant role. In the meantime, the well-studied subject of DNA binding proteins that diffuse along the DNA backbone provides an insightful analog for understanding the nature of microtubule-based diffusional motility.

摘要

基于微管的运动通常被认为具体是指基于微管的马达(如驱动蛋白或动力蛋白)的定向步进。然而,微管晶格扩散(也称为扩散运动)提供了第二种运输模式,这种模式为更广泛的一类微管结合蛋白所共有。微管晶格扩散作为一种运输机制具有明显优势,包括速度、双向微管末端靶向以及无需直接化学能(即ATP)。这种相互作用的通用结合机制是否会被确定还有待观察,但静电相互作用似乎起着重要作用。与此同时,对沿DNA主链扩散的DNA结合蛋白这一研究充分的课题进行研究,为理解基于微管的扩散运动的本质提供了一个有启发性的类比。

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