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细胞中的驱动蛋白组装和运动。

Kinesin assembly and movement in cells.

机构信息

Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.

出版信息

Annu Rev Biophys. 2011;40:267-88. doi: 10.1146/annurev-biophys-042910-155310.

Abstract

Long-distance transport in eukaryotic cells is driven by molecular motors that move along microtubule tracks. Molecular motors of the kinesin superfamily contain a kinesin motor domain attached to family-specific sequences for cargo binding, regulation, and oligomerization. The biochemical and biophysical properties of the kinesin motor domain have been widely studied, yet little is known about how kinesin motors work in the complex cellular environment. We discuss recent studies on the three major families involved in intracellular transport (kinesin-1, kinesin-2, and kinesin-3) that have begun to bridge the gap in knowledge between the in vitro and in vivo behaviors of kinesin motors. These studies have increased our understanding of how kinesin subunits assemble to produce a functional motor, how kinesin motors are affected by biochemical cues and obstacles present on cellular microtubules, and how multiple motors on a cargo surface can work collectively for increased force production and travel distance.

摘要

真核细胞中的长距离运输是由沿着微管轨道运动的分子马达驱动的。驱动蛋白超家族的分子马达包含一个驱动蛋白马达结构域,该结构域连接着用于货物结合、调节和寡聚化的家族特异性序列。驱动蛋白马达结构域的生化和生物物理特性已经得到了广泛的研究,但对于驱动蛋白马达在复杂的细胞环境中如何工作,我们知之甚少。我们讨论了最近关于参与细胞内运输的三个主要家族(驱动蛋白-1、驱动蛋白-2 和驱动蛋白-3)的研究,这些研究开始弥合驱动蛋白马达在体外和体内行为之间的知识差距。这些研究增加了我们对驱动蛋白亚基如何组装产生功能马达的理解,以及驱动蛋白马达如何受到细胞微管上存在的生化线索和障碍物的影响,以及货物表面上的多个马达如何共同工作以增加力的产生和行进距离。

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