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Motor Dynamics Underlying Cargo Transport by Pairs of Kinesin-1 and Kinesin-3 Motors

机译:一对Kinesin-1和Kinesin-3电动机在货物运输过程中的电动机动力学

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摘要

Intracellular cargo transport by kinesin family motor proteins is crucial for many cellular processes, particularly vesicle transport in axons and dendrites. In a number of cases, the transport of specific cargo is carried out by two classes of kinesins that move at different speeds and thus compete during transport. Despite advances in single-molecule characterization and modeling approaches, many questions remain regarding the effect of intermotor tension on motor attachment/reattachment rates during cooperative multimotor transport. To understand the motor dynamics underlying multimotor transport, we analyzed the complexes of kinesin-1 and kinesin-3 motors attached through protein scaffolds moving on immobilized microtubules in vitro. To interpret the observed behavior, simulations were carried out using a model that incorporated motor stepping, attachment/detachment rates, and intermotor force generation. In single-molecule experiments, isolated kinesin-3 motors moved twofold faster and had threefold higher landing rates than kinesin-1. When the positively charged loop 12 of kinesin-3 was swapped with that of kinesin-1, the landing rates reversed, indicating that this “K-loop” is a key determinant of the motor reattachment rate. In contrast, swapping loop 12 had negligible effects on motor velocities. Two-motor complexes containing one kinesin-1 and one kinesin-3 moved at different speeds depending on the identity of their loop 12, indicating the importance of the motor reattachment rate on the cotransport speed. Simulations of these loop-swapped motors using experimentally derived motor parameters were able to reproduce the experimental results and identify best fit parameters for the motor reattachment rates for this geometry. Simulation results also supported previous work, suggesting that kinesin-3 microtubule detachment is very sensitive to load. Overall, the simulations demonstrate that the transport behavior of cargo carried by pairs of kinesin-1 and -3 motors are determined by three properties that differ between these two families: the unloaded velocity, the load dependence of detachment, and the motor reattachment rate.
机译:驱动蛋白家族运动蛋白通过细胞内货物运输对许多细胞过程至关重要,特别是轴突和树突中的囊泡运输。在许多情况下,特定货物的运输是通过两类驱动蛋白进行的,它们以不同的速度运动,因此在运输过程中相互竞争。尽管在单分子表征和建模方法方面取得了进步,但在协作多电机运输过程中,电机间张力对电机连接/重新连接速率的影响仍然存在许多问题。为了了解多马达运输基础的马达动力学,我们分析了通过在固定的微管上移动的蛋白质支架附着的kinesin-1和kinesin-3马达的复合物。为了解释观察到的行为,使用包含电机步进,附着/脱离速率和电机间力生成的模型进行了模拟。在单分子实验中,独立的kinesin-3电动机的移动速度比kinesin-1快两倍,并且着陆速率高三倍。当驱动蛋白3的带正电荷的回路12与驱动蛋白1的带正电荷的回路交换时,着陆速率反转,表明该“ K回路”是决定电机重新连接速率的关键因素。相反,交换回路12对电动机速度的影响可忽略不计。包含一种驱动蛋白-1和一种驱动蛋白3的两种运动复合物以不同的速度移动,这取决于它们的环12的特性,表明运动再附着速率对共同运输速度的重要性。使用实验得出的电动机参数对这些环路交换电动机进行的仿真能够重现实验结果,并为该几何形状的电动机重新连接速度确定最佳拟合参数。仿真结果也支持以前的工作,表明kinesin-3微管分离对负荷非常敏感。总体而言,模拟表明,成对的kinesin-1和-3电机对的运输行为由这两个系列之间不同的三个属性决定:空载速度,分离的负载依赖性以及电机的重新连接速度。

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