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Nir. S. Gov

Publications and source records attributed to Nir. S. Gov.

2 recordsLinked to original sources

Activity controls fragility: A Random First Order Transition Theory for an active glass

How does nonequilibrium activity modify the approach to a glass? This is an important question, since many experiments reveal the near-glassy nature of the cell interior, remodelled by activity. However, different simulations of dense assemblies of active particles, parametrised by a self-propulsion force, $f_0$, and persistence time, $τ_p$, appear to make contradictory predictions about the influence of activity on characteristic features of glass, such as fragility. This calls for a broad conceptual framework to understand active glasses; here we extend the Random First-Order Transition (RFOT) theory to a dense assembly of self-propelled particles. We compute the active contribution to the configurational entropy using an effective medium approach - that of a single particle in a caging-potential. This simple active extension of RFOT provides excellent quantitative fits to existing simulation results. We find that whereas $f_0$ always inhibits glassiness, the effect of $τ_p$ is more subtle and depends on the microscopic details of activity. In doing so, the theory automatically resolves the apparent contradiction between the simulation models. The theory also makes several testable predictions, which we verify by both existing and new simulation data, and should be viewed as a step towards a more rigorous analytical treatment of active glass.

cond-mat.soft

Theory of epithelial cell shape transitions induced by mechanoactive chemical gradients

Cell shape is determined by a balance of intrinsic properties of the cell as well as its mechanochemical environment. Inhomogeneous shape changes underly many morphogenetic events and involve spatial gradients in active cellular forces induced by complex chemical signaling. Here, we introduce a mechanochemical model based on the notion that cell shape changes may be induced by external diffusible biomolecules that influence cellular contractility (or equivalently, adhesions) in a concentration-dependent manner -- and whose spatial profile in turn is affected by cell shape. We map out theoretically the possible interplay between chemical concentration and cellular structure. Besides providing a direct route to spatial gradients in cell shape profiles in tissues, our results indicate that the dependence on cell shape helps create robust mechanochemical gradients.

physics.bio-ph