Nonuniform filament turnover, contractility, and bundle formation in disordered actomyosin networks
Alexander K Y Tam1, Alex Mogilner2, Dietmar B Oelz3
1UniSA STEM, The University of South Australia, Mawson Lakes, South Australia, Australia.
Biophysical Journal
|February 27, 2026
Summary
Actomyosin networks require filament turnover for sustained contractility. Different turnover pathways balance bundle formation and contractility, offering cells control over network dynamics.
Area of Science:
- Cellular mechanics
- Biophysics
- Computational biology
Background:
- Actomyosin networks are crucial for cellular functions like contraction and structure.
- Filament turnover and mechanics significantly impact network behavior.
- Understanding these dynamics is key to cellular processes.
Purpose of the Study:
- To investigate how filament turnover and mechanics influence contractility and bundle formation in disordered actomyosin networks.
- To compare the effects of four distinct filament turnover models: uniform, biased, branching, and treadmilling.
- To explore the relationship between filament flexibility, crosslinking friction, and network properties.
Main Methods:
- Utilized a two-dimensional agent-based model for actomyosin networks.
- Simulated four simplified models of filament turnover.
- Analyzed contractility, bundle formation, and network patterns under different turnover conditions.
- Investigated the impact of filament bendability and crosslinking friction.
Main Results:
- Networks without turnover lose contractility and form static bundles.
- Introducing filament turnover enhances and prolongs contractility.
- Uniform turnover disrupts bundles but maintains contractility.
- Non-uniform turnover models (biased, branching, treadmilling) promote bundle formation while allowing sustained contractility.
- Branching at 70° favors contractility; treadmilling affects the trade-off.
- Biased turnover enhances bundles but reduces contractility persistence.
- More flexible filaments increase bundle formation; higher crosslinking friction boosts contractility.
Conclusions:
- Filament turnover is essential for persistent contractility in actomyosin networks.
- Cells can regulate contractility and bundle formation by modulating actin turnover pathways.
- Specific turnover mechanisms offer distinct trade-offs between bundle formation and contractility, providing tunable control over network mechanics.
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