Direct detection of deformation modes on varying length scales in active biopolymer networks.

Samantha Stam, Margaret L Gardel, Kimberly L Weirich
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Abstract

Correlated flows and forces that emerge from active matter orchestrate complex processes such as shape regulation and deformations in biological cells and tissues. The active materials central to cellular mechanics are cytoskeletal networks, where molecular motor activity drives deformations and remodeling. Here, we investigate deformation modes in contractile actin networks driven by the molecular motor myosin II through quantitative fluorescence microscopy. We examine the deformation anisotropy at different length scales in networks of sparsely cross-linked and bundled actin. In sparsely cross-linked networks, we find myosin-dependent biaxial buckling modes across length scales. Interestingly, both long and short-wavelength buckling may contribute to network contractility. In cross-linked bundled networks, uniaxial contraction predominates on long length scales, while the uniaxial or biaxial nature of the deformation depends on bundle microstructure at shorter length scales. The anisotropy of deformations may provide insight to the mechanical origins of contractility in actin networks and regulation of collective behavior in a variety of active materials.

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直接检测活性生物聚合物网络中不同长度尺度上的变形模式。
活性物质产生的相关流动和力协调了复杂的过程,如生物细胞和组织的形状调节和变形。细胞力学的核心活性物质是细胞骨架网络,分子运动活动驱动变形和重塑。在这里,我们通过定量荧光显微镜研究了分子运动肌球蛋白II驱动的肌动蛋白网络中的变形模式。我们研究了纠缠、交联和成束肌动蛋白网络在不同长度尺度上的变形各向异性。在稀疏交联的网络中,我们发现了长度尺度上肌球蛋白依赖的双轴屈曲模式。在交联成束网络中,单轴收缩在长长度尺度上占主导地位,而变形的单轴或双轴性质取决于较短长度尺度上的成束微观结构。变形的各向异性可以为各种活性材料中集体行为的调节提供见解。
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