Living systems exhibit self-organization, a phenomenon that enables organisms to perform functions essential for life. The interior of living cells is a crowded environment in which the self-assembly of cytoskeletal networks is spatially constrained by membranes and organelles. Cytoskeletal filaments undergo active condensation in the presence of crosslinking motor proteins. In past studies, confinement has been shown to alter the morphology of active condensates. Here, we perform simulations to explore systems of filaments and crosslinking motors in a variety of confining geometries. We simulate spatial confinement imposed by hard spherical, cylindrical, and planar boundaries. These systems exhibit non-equilibrium condensation behavior where crosslinking motors condense a fraction of the overall filament population, leading to coexistence of vapor and condensed states. We find that the confinement lengthscale modifies the dynamics and condensate morphology. With end-pausing crosslinking motors, filaments self-organize into half asters and fully-symmetric asters under spherical confinement, polarity-sorted bilayers and bottle-brush-like states under cylindrical confinement, and flattened asters under planar confinement. The number of crosslinking motors controls the size and shape of condensates, with flattened asters becoming hollow and ring-like for larger motor number. End pausing plays a key role affecting condensate morphology: systems with end-pausing motors evolve into aster-like condensates while those with non-end-pausing crosslinking motor proteins evolve into disordered clusters and polarity-sorted bundles.
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Extensile to contractile transition in active microtubule–actin composites generates layered asters with programmable lifetimes
Significance Active forces sculpt the forms of living things, generating adaptable and reconfigurable dynamical materials. Creating synthetic materials that exhibit comparable control over internally generated active forces remains a challenge. We demonstrate that active composite networks, collectively driven by the force-generating molecular motors, exhibit complex spatiotemporal patterns similar to those observed in cell biology. Amongst others, we describe robust self-assembly of onion-like layered asters. A self-regulating mechanism ensures the asters’ layered structure survives coalescence-like events, while their temporal stability is encoded in the mechanical properties of the network. Our model system elucidates the essential role of passive elasticity in controlling the emergent nonequilibrium dynamics while also establishing a robust experimental platform for engineering lifelike materials.
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- Award ID(s):
- 2011846
- PAR ID:
- 10506794
- Publisher / Repository:
- National Academy of Sciences
- Date Published:
- Journal Name:
- Proceedings of the National Academy of Sciences
- Volume:
- 119
- Issue:
- 5
- ISSN:
- 0027-8424
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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