Growth-induced collective bending and kinetic trapping of cytoskeletal filaments

IF 2.4 4区 生物学 Q4 CELL BIOLOGY
Cytoskeleton Pub Date : 2024-05-22 DOI:10.1002/cm.21877
Deb Sankar Banerjee, Simon L. Freedman, Michael P. Murrell, Shiladitya Banerjee
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引用次数: 0

Abstract

Growth and turnover of actin filaments play a crucial role in the construction and maintenance of actin networks within cells. Actin filament growth occurs within limited space and finite subunit resources in the actin cortex. To understand how filament growth shapes the emergent architecture of actin networks, we developed a minimal agent-based model coupling filament mechanics and growth in a limiting subunit pool. We find that rapid filament growth induces kinetic trapping of highly bent actin filaments. Such collective bending patterns are long-lived, organized around nematic defects, and arise from competition between filament polymerization and bending elasticity. The stability of nematic defects and the extent of kinetic trapping are amplified by an increase in the abundance of the actin pool and by crosslinking the network. These findings suggest that kinetic trapping is a robust consequence of growth in crowded environments, providing a route to program shape memory in actin networks.

Abstract Image

生长诱导的细胞骨架丝的集体弯曲和动力学捕获
肌动蛋白丝的生长和更替在细胞内肌动蛋白网络的构建和维持中起着至关重要的作用。肌动蛋白丝的生长发生在肌动蛋白皮层有限的空间和有限的亚基资源内。为了了解肌动蛋白丝的生长是如何形成肌动蛋白网络的新兴结构的,我们开发了一个基于最小代理的模型,该模型将肌动蛋白丝力学与有限亚基池中的生长耦合在一起。我们发现,丝状物的快速生长会诱发高度弯曲的肌动蛋白丝的动力学捕获。这种集体弯曲模式持续时间长,围绕向列缺陷组织,产生于丝聚合和弯曲弹性之间的竞争。肌动蛋白池丰度的增加和网络的交联扩大了向列缺陷的稳定性和动力学诱捕的程度。这些发现表明,动力学陷阱是在拥挤环境中生长的一个强有力的结果,为肌动蛋白网络的形状记忆编程提供了一条途径。
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来源期刊
Cytoskeleton
Cytoskeleton CELL BIOLOGY-
CiteScore
5.50
自引率
3.40%
发文量
24
审稿时长
6-12 weeks
期刊介绍: Cytoskeleton focuses on all aspects of cytoskeletal research in healthy and diseased states, spanning genetic and cell biological observations, biochemical, biophysical and structural studies, mathematical modeling and theory. This includes, but is certainly not limited to, classic polymer systems of eukaryotic cells and their structural sites of attachment on membranes and organelles, as well as the bacterial cytoskeleton, the nucleoskeleton, and uncoventional polymer systems with structural/organizational roles. Cytoskeleton is published in 12 issues annually, and special issues will be dedicated to especially-active or newly-emerging areas of cytoskeletal research.
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