Department of Mechanical Engineering, The University of Hong Kong, Hong Kong, China.
Biophys J. 2010 Aug 9;99(4):1043-52. doi: 10.1016/j.bpj.2010.06.001.
Using a generalized Brownian ratchet model that accounts for the interactions of actin filaments with the surface of Listeria mediated by proteins like ActA and Arp2/3, we have developed a microscopic model for the movement of Listeria. Specifically, we show that a net torque can be generated within the comet tail, causing the bacteria to spin about its long axis, which in conjunction with spatially varying polymerization at the surface leads to motions of bacteria in curved paths that include circles, sinusoidal-like curves, translating figure eights, and serpentine shapes, as observed in recent experiments. A key ingredient in our formulation is the coupling between the motion of Listeria and the force-dependent rate of filament growth. For this reason, a numerical scheme was developed to determine the kinematic parameters of motion and stress distribution among filaments in a self-consistent manner. We find that a 5-15% variation in polymerization rates can lead to radii of curvatures of the order of 4-20 microm, measured in experiments. In a similar way, our results also show that most of the observed trajectories can be produced by a very low degree of correlation, <10%, among filament orientations. Since small fluctuations in polymerization rate, as well as filament orientation, can easily be induced by various factors, our findings here provide a reasonable explanation for why Listeria can travel along totally different paths under seemingly identical experimental conditions. Besides trajectories, stress distributions corresponding to different polymerization profiles are also presented. We have found that although some actin filaments generate propelling forces that push the bacteria forward, others can exert forces opposing the movement of Listeria, consistent with recent experimental observations.
利用一个广义的布朗棘轮模型,该模型考虑了肌动蛋白丝与 ActA 和 Arp2/3 等蛋白介导的李斯特菌表面的相互作用,我们为李斯特菌的运动开发了一个微观模型。具体来说,我们表明,在彗尾内可以产生净扭矩,导致细菌围绕其长轴旋转,这与表面上空间变化的聚合作用相结合,导致细菌在弯曲路径中运动,包括圆、正弦样曲线、平移的 8 字形和蛇形,如最近的实验观察到的那样。我们的公式中的一个关键成分是李斯特菌的运动与力依赖性丝生长速率之间的耦合。因此,开发了一种数值方案来以自洽的方式确定运动的运动学参数和丝之间的应力分布。我们发现聚合速率的 5-15%变化可以导致曲率半径为 4-20 微米,这与实验测量值一致。以类似的方式,我们的结果还表明,通过丝取向之间的<10%的非常低的相关性,可以产生大部分观察到的轨迹。由于聚合速率以及丝取向的微小波动很容易被各种因素诱导,因此我们的发现为为什么李斯特菌可以在看似相同的实验条件下沿着完全不同的路径运动提供了合理的解释。除了轨迹之外,还呈现了对应于不同聚合分布的应力分布。我们发现,尽管一些肌动蛋白丝产生推动细菌向前的推进力,但其他丝可以产生与李斯特菌运动相反的力,这与最近的实验观察结果一致。