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首页> 外文期刊>Biophysical Journal >Motor Dynamics Underlying Cargo Transport by Pairs of Kinesin-1 and Kinesin-3 Motors
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Motor Dynamics Underlying Cargo Transport by Pairs of Kinesin-1 and Kinesin-3 Motors

机译:通过成对的Kinesin-1和Kinesin-3电机底层货物运输潜水动态

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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:Kinesin家族马达蛋白的细胞内货物运输对于许多细胞过程至关重要,特别是轴突和树突中的囊泡输送。在许多情况下,特定货物的运输由两类以不同速度移动,从而在运输过程中进行竞争。尽管单分子表征和建模方法进行了进展,但许多问题仍然是在合作多电机运输期间对电动机附着/重新附接速率的影响。要了解多电机传输的电动机动力学,我们分析了通过在体外移动的蛋白质支架上连接的Kinesin-1和Kinesin-3电机的复合物。为了解释观察到的行为,使用掺入电动机踩踏,附接/分离速率和隔离力产生的模型进行仿真。在单分子实验中,孤立的Kinesin-3电动机移动得更快,并且比Kinesin-1更高的着陆率具有三倍。当Kinesin-3的带正电荷的环12与Kinesin-1的带电环绕时,颠倒的着陆速率,表明该“K-Loop”是电机ReatClachment率的关键决定因素。相比之下,交换环12具有对电动机速度的可忽略效果。含有一个Kinesin-1和一个Kinesin-3的双电动机复合物根据它们的环12的身份,表示电机重新连接率对Cotransport速度的重要性。这些环的模拟 - 使用实验衍生的电动机参数的开箱电机能够再现实验结果,并确定该几何的电机重新连接率的最佳拟合参数。模拟结果也支持以前的工作,表明Kinesin-3微管脱离对负荷非常敏感。总体而言,模拟表明,由kinesin-1和-3电动机成对携带的货物的运输行为由不同赌注的三种性质确定威森这两个家庭:卸载的速度,拆卸的负荷依赖性,以及电机重新连接率。

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