Kim Taeyoon, Hwang Wonmuk, Lee Hyungsuk, Kamm Roger D
Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
PLoS Comput Biol. 2009 Jul;5(7):e1000439. doi: 10.1371/journal.pcbi.1000439. Epub 2009 Jul 17.
Mechanical force plays an important role in the physiology of eukaryotic cells whose dominant structural constituent is the actin cytoskeleton composed mainly of actin and actin crosslinking proteins (ACPs). Thus, knowledge of rheological properties of actin networks is crucial for understanding the mechanics and processes of cells. We used Brownian dynamics simulations to study the viscoelasticity of crosslinked actin networks. Two methods were employed, bulk rheology and segment-tracking rheology, where the former measures the stress in response to an applied shear strain, and the latter analyzes thermal fluctuations of individual actin segments of the network. It was demonstrated that the storage shear modulus (G') increases more by the addition of ACPs that form orthogonal crosslinks than by those that form parallel bundles. In networks with orthogonal crosslinks, as crosslink density increases, the power law exponent of G' as a function of the oscillation frequency decreases from 0.75, which reflects the transverse thermal motion of actin filaments, to near zero at low frequency. Under increasing prestrain, the network becomes more elastic, and three regimes of behavior are observed, each dominated by different mechanisms: bending of actin filaments, bending of ACPs, and at the highest prestrain tested (55%), stretching of actin filaments and ACPs. In the last case, only a small portion of actin filaments connected via highly stressed ACPs support the strain. We thus introduce the concept of a 'supportive framework,' as a subset of the full network, which is responsible for high elasticity. Notably, entropic effects due to thermal fluctuations appear to be important only at relatively low prestrains and when the average crosslinking distance is comparable to or greater than the persistence length of the filament. Taken together, our results suggest that viscoelasticity of the actin network is attributable to different mechanisms depending on the amount of prestrain.
机械力在真核细胞生理学中起着重要作用,真核细胞的主要结构成分是主要由肌动蛋白和肌动蛋白交联蛋白(ACPs)组成的肌动蛋白细胞骨架。因此,了解肌动蛋白网络的流变特性对于理解细胞的力学和过程至关重要。我们使用布朗动力学模拟来研究交联肌动蛋白网络的粘弹性。采用了两种方法,整体流变学和片段追踪流变学,前者测量响应施加剪切应变的应力,后者分析网络中单个肌动蛋白片段的热涨落。结果表明,与形成平行束的ACPs相比,添加形成正交交联的ACPs时储能剪切模量(G')增加得更多。在具有正交交联的网络中,随着交联密度的增加,G'作为振荡频率函数的幂律指数从0.75(反映肌动蛋白丝的横向热运动)降低到低频时接近零。在预应变增加的情况下,网络变得更具弹性,观察到三种行为模式,每种模式由不同机制主导:肌动蛋白丝的弯曲、ACPs的弯曲,以及在测试的最高预应变(55%)下,肌动蛋白丝和ACPs的拉伸。在最后一种情况下,只有一小部分通过高应力ACPs连接的肌动蛋白丝支持应变。因此,我们引入了“支撑框架”的概念,作为完整网络的一个子集,它负责高弹性。值得注意的是,由于热涨落引起的熵效应似乎仅在相对较低的预应变以及平均交联距离与丝的持久长度相当或更大时才重要。综上所述,我们的结果表明,肌动蛋白网络的粘弹性取决于预应变的量,由不同机制引起。