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Significance This manuscript addresses the role of active processes in the spatial organization and dynamics of cell surface components. Using a reconstituted minimal system, we provide experimental evidence for a proposed clustering mechanism that relies on the intrinsic, active mechanics of actin filaments and myosin motors expected to be present at the cell cortex. The coupling between the actomyosin and the lipid bilayer gives rise to an emergent active composite with properties that resemble those observed in live cells. This clustering mechanism is a key feature of the active composite cell surface model and furthers our understanding of the multiple ways in which the cell surface might regulate its composition.

Actomyosin dynamics drive local membrane component organization in an in vitro active composite layer