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驱动蛋白定向运动的调控。

Regulation of kinesin-directed movements.

作者信息

Haimo L T

机构信息

Dept of Biology, University of California, Riverside, CA 92521, USA.

出版信息

Trends Cell Biol. 1995 Apr;5(4):165-8. doi: 10.1016/s0962-8924(00)88981-3.

Abstract

Bidirectional organelle transport along microtubules is most likely mediated by the opposing forces generated by two microtubule-based motors: kinesin and cytoplasmic dynein. Because the direction and timing of organelle movements are controlled by the cell, the activity of one or both of these motor molecules must be regulated. Recent studies demonstrate that kinesin, kinesin-like proteins and kinesin-associated proteins can be phosphorylated, and suggest that changes in their phosphorylation state may modulate kinesin's ability to interact with either microtubules or organelles. Thus, it is possible that phosphorylation regulates kinesin-driven movements.

摘要

沿微管的双向细胞器运输很可能是由两种基于微管的马达产生的相反力量介导的

驱动蛋白和细胞质动力蛋白。由于细胞器运动的方向和时间是由细胞控制的,因此这些马达分子中的一个或两个的活性必须受到调节。最近的研究表明,驱动蛋白、驱动蛋白样蛋白和驱动蛋白相关蛋白可以被磷酸化,并表明它们磷酸化状态的变化可能调节驱动蛋白与微管或细胞器相互作用的能力。因此,磷酸化有可能调节由驱动蛋白驱动的运动。

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