Comparing simulations of actin filament compression reveals tradeoff between computational cost and capturing supertwist.

microPublication biology Pub Date : 2025-01-21 eCollection Date: 2025-01-01 DOI:10.17912/micropub.biology.001347
Blair Lyons, Saurabh S Mogre, Karthik Vegesna, Jessica S Yu, Mark Hansen, Aadarsh Raghunathan, Graham T Johnson, Eran Agmon, Matthew Akamatsu
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引用次数: 0

Abstract

The dynamic bending and twisting of actin drives numerous cellular processes. To compare how different spatial scales in actin models capture these dynamics, we developed two models of actin filaments: one at monomer-scale using ReaDDy and one at fiber-scale using Cytosim. Simulating filament compression across a range of velocities, we found a divergence between the monomer- and fiber-scale simulations; notably, the monomer-scale simulations more effectively captured filament supertwist, characteristic of helical structure, but at a higher computational cost. Such comparisons can aid in designing more efficient and accurate multi-scale biological models. Interactive visualizations at https://simularium.github.io/subcell-website.

对比模拟肌动蛋白丝压缩揭示了计算成本和捕获超捻之间的权衡。
肌动蛋白的动态弯曲和扭曲驱动着许多细胞过程。为了比较不同空间尺度的肌动蛋白模型如何捕捉这些动态,我们开发了两种肌动蛋白细丝模型:一种是使用ReaDDy的单体尺度模型,另一种是使用Cytosim的纤维尺度模型。在一定速度范围内模拟长丝压缩,我们发现单体和纤维尺度模拟之间存在分歧;值得注意的是,单体尺度的模拟更有效地捕获了丝的超捻,这是螺旋结构的特征,但计算成本较高。这种比较有助于设计更有效和准确的多尺度生物模型。可在https://simularium.github.io/subcell-website获得交互式可视化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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