Hydrodynamic effects on spinodal decomposition kinetics in planar lipid bilayer membranes

被引:49
作者
Fan, Jun [1 ]
Han, Tao
Haataja, Mikko [1 ,2 ]
机构
[1] Princeton Univ, Dept Mech & Aerosp Engn, Princeton Inst Sci & Technol Mat PRISM, Princeton, NJ 08544 USA
[2] Princeton Univ, PACM, Princeton, NJ 08544 USA
基金
美国国家科学基金会;
关键词
2-DIMENSIONAL FLUID MIXTURES; PHASE-SEPARATION; BINARY FLUIDS; MOLECULAR-DYNAMICS; DROPLET GROWTH; DOMAINS; VESICLES;
D O I
10.1063/1.3518458
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The formation and dynamics of spatially extended compositional domains in multicomponent lipid membranes lie at the heart of many important biological and biophysical phenomena. While the thermodynamic basis for domain formation has been explored extensively in the past, domain growth in the presence of hydrodynamic interactions both within the (effectively) two-dimensional membrane and in the three-dimensional solvent in which the membrane is immersed has received little attention. In this work, we explore the role of hydrodynamic effects on spinodal decomposition kinetics via continuum simulations of a convective Cahn-Hilliard equation for membrane composition coupled to the Stokes equation. Our approach explicitly includes hydrodynamics both within the planar membrane and in the three-dimensional solvent in the viscously dominated flow regime. Numerical simulations reveal that dynamical scaling breaks down for critical lipid mixtures due to distinct coarsening mechanisms for elongated versus more isotropic compositional lipid domains. The breakdown in scaling should be readily observable in experiments on model membrane systems. (c) 2010 American Institute of Physics. [doi:10.1063/1.3518458]
引用
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页数:10
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