Mechanochemical feedback between confinement and actin crosslinking drives the shape dynamics of liquid-like droplets.

Several actin-binding proteins can form liquid-liquid phase-separated condensates that promote actin filament assembly and bundling, which is crucial for local actin network organization. Previous studies have established that phase-separated condensates composed of actin-binding proteins, such as vasodilator-stimulated phosphoprotein (VASP) and Lamellipodin (Lpd), restrict the organization of actin filaments to structures such as rings, shells, discs, and rods through kinetic trapping. However, the mechanism by which crosslinker multivalency, actin growth, and condensate properties tune actin organization and droplet shape is not well understood. Using a combination of agent-based simulations and experiments, we find that the deformability of the droplet interface allows for the emergence of not just tightly-bundled actin rings but also weakly-bundled actin discs. We find two major quantitative relationships between actin bundling and droplet deformation. The first relationship shows that the crosslinked bundle thickness and droplet diameter followed a power law, consistent with experiments. The second one is that the kinetics of droplet deformation follows a dynamic snapping behavior that depends on the droplet surface tension and the multivalent VASP-actin binding kinetics. We predicted that these two relationships were generalizable to dynamic multimers and to weak actin crosslinkers. Our predictions were experimentally tested using two additional condensate-forming proteins, lamellipodin and RGG. Taken together, we show that mechanochemical feedback between the droplet interface properties and crosslinker multivalency tune actin organization and control the dynamics of droplet deformation by actin networks.