Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, New Jersey 08544, USA.
J Chem Phys. 2010 Dec 21;133(23):235101. doi: 10.1063/1.3518458.
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.
多组分脂质膜中空间扩展成分域的形成和动力学是许多重要生物和生物物理现象的核心。虽然过去已经广泛研究了域形成的热力学基础,但在(有效)二维膜内以及膜浸入的三维溶剂中存在流体动力学相互作用的情况下,域的生长却很少受到关注。在这项工作中,我们通过对膜成分的对流 Cahn-Hilliard 方程与 Stokes 方程耦合的连续模拟来探索流体动力学效应对旋节分解动力学的作用。我们的方法在粘性主导流中明确地包括了平面膜内和三维溶剂内的流体动力学。数值模拟表明,对于临界脂质混合物,由于长形与更各向同性的成分脂质域的不同粗化机制,动力学标度会发生破坏。在模型膜系统的实验中应该很容易观察到这种标度的破坏。