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Neck linker docking is critical for Kinesin-1 force generation in cells but at a cost to motor speed and processivity

机译:颈部连接器对接对于细胞中Kinesin-1力的产生至关重要但会降低电机的速度和生产率

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摘要

Kinesin force generation involves ATP-induced docking of the neck linker (NL) along the motor core. However, the roles of the proposed steps of NL docking, cover-neck bundle (CNB) and asparagine latch (N-latch) formation, during force generation are unclear. Furthermore, the necessity of NL docking for transport of membrane-bound cargo in cells has not been tested. We generated kinesin-1 motors impaired in CNB and/or N-latch formation based on molecular dynamics simulations. The mutant motors displayed reduced force output and inability to stall in optical trap assays but exhibited increased speeds, run lengths, and landing rates under unloaded conditions. NL docking thus enhances force production but at a cost to speed and processivity. In cells, teams of mutant motors were hindered in their ability to drive transport of Golgi elements (high-load cargo) but not peroxisomes (low-load cargo). These results demonstrate that the NL serves as a mechanical element for kinesin-1 transport under physiological conditions.
机译:驱动蛋白力的产生涉及ATP诱导的颈部接头(NL)沿马达核心的对接。然而,在力产生过程中,NL对接,盖颈束(CNB)和天冬酰胺闩锁(N-latch)形成的建议步骤的作用尚不清楚。此外,NL对接在细胞中运输膜结合货物的必要性尚未得到测试。我们基于分子动力学模拟生成了CNB和/或N闩锁形成受损的kinesin-1电动机。突变电动机显示出减小的力输出并且在光阱测定中无法失速,但是在空载条件下表现出增加的速度,游程长度和着陆速率。因此,NL对接可以提高兵力生产能力,但会降低速度和生产率。在细胞中,成组的突变电动机驱动高尔基元素(高负荷货物)而不是过氧化物酶体(低负荷货物)运输的能力受到阻碍。这些结果表明NL在生理条件下充当驱动蛋白-1运输的机械元件。

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