Affiliation:
1. Department of Chemical Engineering, University of California , Davis, California 95616, USA
Abstract
Biological membranes are self-assembled complex fluid interfaces that host proteins, molecular motors, and other macromolecules essential for cellular function. These membranes have a distinct in-plane fluid response with a surface viscosity that has been well characterized. The resulting quasi-two-dimensional fluid dynamical problem describes the motion of embedded proteins or particles. However, the viscous response of biological membranes is often non-Newtonian: in particular, the surface shear viscosity of phospholipids that comprise the membrane depends strongly on the surface pressure. We use the Lorentz reciprocal theorem to extract the effective long-ranged hydrodynamic interaction among membrane inclusions that arises due to such non-trivial rheology. We show that the corrective force that emerges ties back to the interplay between membrane flow and non-constant viscosity, which suggests a mechanism for biologically favorable protein aggregation within membranes. We quantify and describe the mechanism for such a large-scale concentration instability using a mean-field model. Finally, we employ numerical simulations to demonstrate the formation of hexatic crystals due to the effective hydrodynamic interactions within the membrane.
Subject
Condensed Matter Physics,Fluid Flow and Transfer Processes,Mechanics of Materials,Computational Mechanics,Mechanical Engineering
Cited by
1 articles.
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