Department of Bioengineering, The Pennsylvania State University, University Park, Pennsylvania, United States of America.
PLoS Comput Biol. 2010 Nov 4;6(11):e1000980. doi: 10.1371/journal.pcbi.1000980.
Kinesin stepping is thought to involve both concerted conformational changes and diffusive movement, but the relative roles played by these two processes are not clear. The neck linker docking model is widely accepted in the field, but the remainder of the step--diffusion of the tethered head to the next binding site--is often assumed to occur rapidly with little mechanical resistance. Here, we investigate the effect of tethering by the neck linker on the diffusive movement of the kinesin head, and focus on the predicted behavior of motors with naturally or artificially extended neck linker domains. The kinesin chemomechanical cycle was modeled using a discrete-state Markov chain to describe chemical transitions. Brownian dynamics were used to model the tethered diffusion of the free head, incorporating resistive forces from the neck linker and a position-dependent microtubule binding rate. The Brownian dynamics and chemomechanical cycle were coupled to model processive runs consisting of many 8 nm steps. Three mechanical models of the neck linker were investigated: Constant Stiffness (a simple spring), Increasing Stiffness (analogous to a Worm-Like Chain), and Reflecting (negligible stiffness up to a limiting contour length). Motor velocities and run lengths from simulated paths were compared to experimental results from Kinesin-1 and a mutant containing an extended neck linker domain. When tethered by an increasingly stiff spring, the head is predicted to spend an unrealistically short amount of time within the binding zone, and extending the neck is predicted to increase both the velocity and processivity, contrary to experiments. These results suggest that the Worm-Like Chain is not an adequate model for the flexible neck linker domain. The model can be reconciled with experimental data if the neck linker is either much more compliant or much stiffer than generally assumed, or if weak kinesin-microtubule interactions stabilize the diffusing head near its binding site.
肌球蛋白的步进运动被认为既涉及协同构象变化,也涉及扩散运动,但这两个过程的相对作用尚不清楚。颈部链接器对接模型在该领域被广泛接受,但其余的步骤——即连接的头部扩散到下一个结合位点——通常被认为是快速发生的,阻力很小。在这里,我们研究了颈部链接器的束缚对肌球蛋白头部扩散运动的影响,并重点研究了具有天然或人工延伸颈部链接器域的马达的预测行为。肌球蛋白化学机械循环使用离散状态马尔可夫链来描述化学转变。布朗动力学用于模拟自由头部的束缚扩散,其中包括颈部链接器的阻力和位置相关的微管结合率。布朗动力学和化学机械循环被耦合在一起,以模拟由许多 8nm 步骤组成的进行性运行。研究了三种颈部链接器的力学模型:恒定刚度(简单的弹簧)、增加的刚度(类似于蠕虫链)和反射(在达到限制轮廓长度之前几乎没有刚度)。模拟路径的速度和运行长度与来自 Kinesin-1 和包含延伸颈部链接器域的突变体的实验结果进行了比较。当通过逐渐刚性的弹簧束缚时,头部被预测在结合区域内花费极短的时间,并且延伸颈部被预测会增加速度和进行性,这与实验结果相反。这些结果表明,蠕虫链不是柔性颈部链接器域的合适模型。如果颈部链接器比通常假设的更具顺应性或更刚性,或者如果弱肌球蛋白-微管相互作用稳定扩散头部靠近其结合位点,那么该模型可以与实验数据相一致。