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Biology subjects

Tabatabai, A. P.

Publications and source records attributed to Tabatabai, A. P..

2 recordsLinked to original sources

Mechanical organization yields degenerate dissipation beyond linear response

In non-equilibrium (active) systems, increased driving is commonly assumed to produce proportionally greater energy dissipation. Using picowatt-sensitive calorimetry, entropy-production analysis, rheology, and microscopy in reconstituted actomyosin networks, we show that this relationship breaks down as the material reorganizes under motor activity. Dissipation initially increases with myosin abundance but subsequently decreases despite continued network stiffening, indicating that energetic cost becomes regulated by the evolving mechanical state rather than actuator abundance alone. Comparing catch-bond (-actinin) and slip-bond (fascin) crosslinked networks reveals that bond mechanics shift the critical motor concentration at which this transition occurs, marking the onset of state-dependent energy conversion. Although these networks generate distinct active stresses and mechanical states, they can exhibit comparable dissipation rates, revealing that state-dependent energy conversion can produce degenerate dissipation, whereby mechanically distinct states exhibit similar energetic costs. These findings demonstrate that dissipation in active materials is governed not only by the magnitude of driving but also by the mechanical state that emerges in response to that driving, providing an experimental example of state-dependent energy conversion far from equilibrium.

biophysics↗

Tissue pressure and cell traction compensate to drive robust aggregate spreading

In liquid droplets, the balance of interfacial energies and substrate elasticity determines the shape of the droplet and the dynamics of wetting. In living cells, interfacial energies are not constant, but adapt to the mechanics of their environment. As a result, the forces driving the dynamics of wetting for cells and tissues are unclear and may be context specific. In this work, using a combination of experimental measurements and modeling, we show the surface tension of cell aggregates, as models of active liquid droplets, depends upon the size of the aggregate and the magnitude of applied load, which alters the wetting dynamics. Upon wetting rigid substrates, traction stresses are elevated at the boundary, and tension drives forward motion. By contrast, upon wetting compliant substrates, traction forces are attenuated, yet wetting occurs at a comparable rate. In this case, capillary forces at the contact line are elevated and aggregate surface tension contributes to strong outward, pressure-driven cellular flows. Thus, cell aggregates adapt to the mechanics of their environments, using pressure and traction as compensatory mechanisms to drive robust wetting.

biophysics↗