Kinesin‐Driven De‐Mixing of Cytoskeleton Composites Drives Emergent Mechanical Properties

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Názov: Kinesin‐Driven De‐Mixing of Cytoskeleton Composites Drives Emergent Mechanical Properties
Autori: Janet Sheung, Christopher Gunter, Katarina Matic, Mehrzad Sasanpour, Jennifer L. Ross, Parag Katira, Megan T. Valentine, Rae M. Robertson‐Anderson
Zdroj: Macromol Rapid Commun
Publication Status: Preprint
Informácie o vydavateľovi: Wiley, 2025.
Rok vydania: 2025
Predmety: Soft Condensed Matter (cond-mat.soft), FOS: Physical sciences, Condensed Matter - Soft Condensed Matter, Research Article
Popis: 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. It is discovered 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. It is further shown 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.
Druh dokumentu: Article
Other literature type
Jazyk: English
ISSN: 1521-3927
1022-1336
DOI: 10.1002/marc.202401128
DOI: 10.48550/arxiv.2501.07546
Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/40205878
http://arxiv.org/abs/2501.07546
Rights: CC BY
Prístupové číslo: edsair.doi.dedup.....623f6e9ad13dd2693bc960078bca66de
Databáza: OpenAIRE
Popis
Abstrakt: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. It is discovered 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. It is further shown 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.
ISSN:15213927
10221336
DOI:10.1002/marc.202401128