Cytoskeleton-regulated condensation of integral membrane proteins during cell adhesion.

Understanding protein condensation and its functional implications has been increasingly recognized as crucial for elucidating physiological functions and pathological disorders, as well as for stimulating novel therapeutic strategies. Recent evidence suggests that the cytoskeleton participates in regulating the condensation of cytoplasmic proteins at the cell membrane in adhesion context. By contrast, a fundamental question remains of how the cytoskeleton affects the condensation of the integral membrane proteins during cell adhesion and what functional consequences arise from this process. Using both Monte Carlo simulations and mean field theory, we find that the steric hindrance imposed on adhesion proteins and the protrusive forces exerted on the cell membrane by the cytoskeletal networks can cooperatively drive protein condensation and facilitate phase separation in the cell adhesion system even in the absence of active cytoskeletal transport processes. Meanwhile, our results show that the overall intercellular receptor-ligand interaction can be either enhanced or suppressed during protein condensation, depending sensitively on the interplay between cytoskeleton-protein and cytoskeleton-membrane interactions. Our findings advance our understanding regarding the role of the cytoskeleton in protein condensation and the resulting functional implications.