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驱动蛋白马达和微管交联蛋白 MAP65 对微管的组织作用。

Microtubule organization by kinesin motors and microtubule crosslinking protein MAP65.

机构信息

Department of Physics, University of Massachusetts Amherst, Amherst, MA, USA.

出版信息

J Phys Condens Matter. 2013 Sep 18;25(37):374103. doi: 10.1088/0953-8984/25/37/374103. Epub 2013 Aug 15.

Abstract

Microtubules are rigid, proteinaceous filaments required to organize and rearrange the interior of cells. They organize space by two mechanisms, including acting as the tracks for long-distance cargo transporters, such as kinesin-1, and by forming a network that supports the shape of the cell. The microtubule network is composed of microtubules and a bevy of associated proteins and enzymes that self-organize using non-equilibrium dynamic processes. In order to address the effects of self-organization of microtubules, we have utilized the filament-gliding assay with kinesin-1 motors driving microtubule motion. To further enhance the complexity of the system and determine if new patterns are formed, we added the microtubule crosslinking protein MAP65-1. MAP65-1 is a microtubule-associated protein from plants that crosslinks antiparallel microtubules, similar to mammalian PRC1 and fission yeast Ase1. We find that MAP65 can slow and halt the velocity of microtubules in gliding assays, but when pre-formed microtubule bundles are added to gliding assays, kinesin-1 motors can pull apart the bundles and reconstitute cell-like protrusions.

摘要

微管是刚性的蛋白质丝,需要将细胞内部组织和重新排列。它们通过两种机制组织空间,包括作为长距离货物转运蛋白(如驱动蛋白-1)的轨道,以及形成支撑细胞形状的网络。微管网络由微管和许多相关的蛋白质和酶组成,它们使用非平衡动力学过程自我组织。为了解决微管自组织的影响,我们利用驱动蛋白-1 马达驱动微管运动的丝滑动测定法。为了进一步增加系统的复杂性并确定是否形成新的模式,我们添加了微管交联蛋白 MAP65-1。MAP65-1 是一种来自植物的微管相关蛋白,它交联相反平行的微管,类似于哺乳动物的 PRC1 和裂殖酵母的 Ase1。我们发现 MAP65 可以在滑行测定中减缓和停止微管的速度,但当向滑行测定中添加预先形成的微管束时,驱动蛋白-1 马达可以将束拉开并重新形成类似细胞的突起。

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