Molecular motors robustly drive active gels to a critically connected state

Living systems often exhibit internal driving: active, molecular processes drive nonequilibrium phenomena such as metabolism or migration. Active gels constitute a fascinating class of internally driven matter, where molecular motors exert localized stresses inside polymer networks. There is evidence that network crosslinking is required to allow motors to induce macroscopic contraction. Yet a quantitative understanding of how network connectivity enables contraction is lacking. Here we show experimentally that myosin motors contract crosslinked actin polymer networks to clusters with a scale-free size distribution. This critical behavior occurs over an unexpectedly broad range of crosslink concentrations. To understand this robustness, we develop a quantitative model of contractile networks that takes into account network restructuring: motors reduce connectivity by forcing crosslinks to unbind. Paradoxically, to coordinate global contractions, motor activity should be low. Otherwise, motors drive initially well-connected networks to a critical state where ruptures form across the entire network.Comment: Main text: 21 pages, 5 figures. Supplementary Information: 13 pages, 8 figure

A bottom up approach to cell mechanics

The mechanical stability and integrity of biological cells is provided by the cytoskeleton, a semidilute meshwork of biopolymers. Recent research has underscored its role as a dynamic, multifunctional muscle, whose passive and active mechanical performance is highly heterogeneous in space and time and intimately linked to many biological functions, such that it may serve as a sensitive indicator for the health or developmental state of the cell. In vitro reconstitution of functional modules of the cytoskeleton is now seen as a way of balancing the mutually conflicting demands for simplicity, which is required for systematic and quantitative studies, and for a sufficient degree of complexity that allows a faithful representation of biological functions. This bottom up strategy, aimed at unravelling biological complexity from its physical basis, builds on the latest advances in technology, experimental design and theoreetical modelling, which are reviewed in this progress repor

Multiphase flow models of biogels from crawling cells to bacterial biofilms

This article reviews multiphase descriptions of the fluid mechanics of cytoplasm in crawling cells and growing bacterial biofilms. These two systems involve gels, which are mixtures composed of a polymer network permeated by water. The fluid mechanics of these systems is essential to their biological function and structure. Their mathematical descriptions must account for the mechanics of the polymer, the water, and the interaction between these two phases. This review focuses on multiphase flow models because this framework is natural for including the relative motion between the phases, the exchange of material between phases, and the additional stresses within the network that arise from nonspecific chemical interactions and the action of molecular motors. These models have been successful in accounting for how different forces are generated and transmitted to achieve cell motion and biofilm growth and they have demonstrated how emergent structures develop though the interactions of the two phases. A short description of multiphase flow models of tumor growth is included to highlight the flexibility of the model in describing diverse biological applications