A generalized theoretical framework to investigate multicomponent actin dynamics
The length of actin filaments is regulated by the combined action of hundreds of actin-binding proteins. While the roles of individual proteins are well understood, how they combine to regulate actin dynamics in vivo remains unclear. Recent advances in microscopy have enabled precise, high-throughput measurements of filament lengths over time. However, the absence of a unified theoretical framework has hindered a mechanistic understanding of the multicomponent regulation of actin dynamics. To address this, we propose a general kinetic model that incorporates the combined effects of an arbitrary number of regulatory proteins on actin dynamics. We derive exact closed-form expressions for the moments of (1) the distribution of filament lengths over time and (2) the long-time distribution of changes in filament lengths within a fixed time window. We show that these moments allow us to distinguish between different regulatory mechanisms of multicomponent regulation of actin dynamics. Our theoretical framework provides a powerful tool for interpreting existing data and guiding future experiments.
Authors
- Mintu Nandi (ORCID: https://orcid.org/0000-0002-7720-2693)
- Shashank Shekhar (ORCID: https://orcid.org/0000-0003-1494-0151)
- Sandeep Choubey (ORCID: https://orcid.org/0000-0002-7387-6148)
Institutions
- Emory University (US)
- Homi Bhabha National Institute (IN)
- Institute of Mathematical Sciences (IN)
- Indian Institute of Engineering Science and Technology, Shibpur (IN)
Publication Details
- Journal
- PLoS Computational Biology
- Published
- 2025-09-08
- DOI
- https://doi.org/10.1371/journal.pcbi.1013434
- Primary Topic
- Cellular Mechanics and Interactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00