Kinesin-driven de-mixing of cytoskeleton composites drives emergent mechanical properties

Bibliographic Details
Title: Kinesin-driven de-mixing of cytoskeleton composites drives emergent mechanical properties
Authors: Sheung, Janet, Gunter, Christopher, Matic, Katarina, Sasanpour, Mehrzad, Ross, Jennifer L., Katira, Parag, Valentine, Megan T., Robertson-Anderson, Rae M.
Publication Year: 2025
Collection: Condensed Matter
Subject Terms: Condensed Matter - Soft Condensed Matter
More Details: The cytoskeleton is an active composite of filamentous proteins that dictates diverse mechanical properties and processes in eukaryotic cells by generating forces and autonomously restructuring itself. Enzymatic motors that act on the comprising filaments play key roles in this activity, driving spatiotemporally heterogeneous mechanical responses that are critical to cellular multifunctionality, but also render mechanical characterization challenging. Here, we couple optical tweezers microrheology and fluorescence microscopy with simulations and mathematical modeling to robustly characterize the mechanics of active composites of actin filaments and microtubules restructured by kinesin motors. We discover that composites exhibit a rich ensemble of force response behaviors, elastic, yielding, and stiffening, with their propensity and properties tuned by motor concentration and strain rate. Moreover, intermediate kinesin concentrations elicit emergent mechanical stiffness and resistance while higher and lower concentrations exhibit softer, more viscous dissipation. We further show that composites transition from well-mixed interpenetrating double-networks of actin and microtubules to de-mixed states of microtubule-rich aggregates surrounded by relatively undisturbed actin phases. It is this de-mixing that leads to the emergent mechanical response, offering an alternate route that composites can leverage to achieve enhanced stiffness through coupling of structure and mechanics.
Document Type: Working Paper
Access URL: http://arxiv.org/abs/2501.07546
Accession Number: edsarx.2501.07546
Database: arXiv
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