Kubo Shintaroh, Shima Tomohiro, Takada Shoji
Department of Biophysics, Graduate School of Science, Kyoto University, Kyoto, Japan.
Department of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan.
Biophys J. 2020 Apr 21;118(8):1930-1945. doi: 10.1016/j.bpj.2020.03.012. Epub 2020 Mar 29.
Cytoplasmic dynein is a two-headed molecular motor that moves to the minus end of a microtubule by ATP hydrolysis free energy. By employing its two heads (motor domains), cytoplasmic dynein exhibits various bipedal stepping motions: inchworm and hand-over-hand motions, as well as nonalternating steps of one head. However, the molecular basis to achieve such diverse stepping manners remains unclear because of the lack of an experimental method to observe stepping and the ATPase reaction of dynein simultaneously. Here, we propose a kinetic model for bipedal motions of cytoplasmic dynein and perform Gillespie Monte Carlo simulations that qualitatively reproduce most experimental data obtained to date. The model represents the status of each motor domain as five states according to conformation and nucleotide- and microtubule-binding conditions of the domain. In addition, the relative positions of the two domains were approximated by three discrete states. Accompanied by ATP hydrolysis cycles, the model dynein stochastically and processively moved forward in multiple steps via diverse pathways, including inchworm and hand-over-hand motions, similarly to experimental data. The model reproduced key experimental motility-related properties, including velocity and run length, as functions of the ATP concentration and external force, therefore providing a plausible explanation of how dynein achieves various stepping manners with explicit characterization of nucleotide states. Our model highlights the uniqueness of dynein in the coupling of ATPase with its movement during both inchworm and hand-over-hand stepping.
细胞质动力蛋白是一种双头分子马达,通过ATP水解自由能向微管的负端移动。通过利用其两个头部(马达结构域),细胞质动力蛋白表现出各种双足步进运动:尺蠖式和换手式运动,以及一个头部的非交替步。然而,由于缺乏同时观察动力蛋白步进和ATP酶反应的实验方法,实现这种多样步进方式的分子基础仍不清楚。在这里,我们提出了一个细胞质动力蛋白双足运动的动力学模型,并进行了吉莱斯皮蒙特卡罗模拟,定性地再现了迄今为止获得的大多数实验数据。该模型根据结构域的构象、核苷酸和微管结合条件,将每个马达结构域的状态表示为五种状态。此外,两个结构域的相对位置通过三种离散状态进行近似。伴随着ATP水解循环,模型中的动力蛋白通过多种途径(包括尺蠖式和换手式运动)随机且连续地向前多步移动,类似于实验数据。该模型再现了关键的与运动性相关的实验特性,包括速度和运行长度,作为ATP浓度和外力的函数,因此通过对核苷酸状态进行明确表征,为动力蛋白如何实现各种步进方式提供了一个合理的解释。我们的模型突出了动力蛋白在尺蠖式和换手式步进过程中ATP酶与其运动耦合方面的独特性。