Dynamic lateral transport of lipids, proteins, and self-assembled structures
in biomembranes plays crucial roles in diverse cellular processes. In this
study, we perform a coarse-grained molecular dynamics simulation on a vesicle
composed of a binary mixture of neutral and anionic lipids to investigate the
lateral transport of individual lipid molecules and the self-assembled lipid
domains upon an applied direct current (DC) electric field. Under the potential
force of the electric field, a phase-separated domain rich in the anionic
lipids is trapped in the opposite direction of the electric field. The
subsequent reversal of the electric field induces the unidirectional domain
motion. During the domain motion, the domain size remains constant, but a
considerable amount of the anionic lipids is exchanged between the
anionic-lipid-rich domain and the surrounding bulk. While the speed of the
domain motion (collective lipid motion) shows a significant positive
correlation with the electric field strength, the exchange of anionic lipids
between the domain and bulk (individual lipid motion) exhibits no clear
correlation with the field strength. The mean velocity field of the lipids
surrounding the domain displays a two-dimensional (2D) source dipole. We
revealed that the balance between the potential force of the applied electric
field and the quasi-2D hydrodynamic frictional force well explains the
dependence of the domain motions on the electric-field strengths. The present
results provide insight into the hierarchical dynamic responses of
self-assembled lipid domains to the applied electric field and contribute to
controlling the lateral transportation of lipids and membrane inclusions.Comment: 9 pages, 6 figure