Related papers: Cylindrical equilibrium shapes of fluid membranes
In this paper we investigate constant mean curvature surfaces with nonempty boundary in Euclidean space that meet a right cylinder at a constant angle along the boundary. If the surface lies inside of the cylinder, we obtain some results of…
We consider a diffuse interface approximation for the lipid phases of rotationally symmetric two-phase bilayer membranes and rigorously derive its $\Gamma$-limit. In particular, we prove that limit vesicles are $C^1$ across interfaces,…
The disk-to-vesicle transition of a fluid membrane with no spontaneous curvature is well described by the competition between edge line and curvature energies. However, the transition of asymmetric membranes with spontaneous curvatures is…
The stresses in a closed lipid membrane described by the Helfrich hamiltonian, quadratic in the extrinsic curvature, are identified using Noether's theorem. Three equations describe the conservation of the stress tensor: the normal…
Polyhedral vesicles with a large bending modulus of the membrane such as the gel phase lipid membrane were studied using a Brownian dynamics simulation. The vesicles exhibit various polyhedral morphologies such as tetrahedron and cube…
Consider a surface, enclosing a fixed volume, described by a free-energy depending only on the local geometry; for example, the Canham-Helfrich energy quadratic in the mean curvature describes a fluid membrane. The stress at any point on…
We study, using dissipative particle dynamics simulations, the effect of active lipid flip-flop on model fluid bilayer membranes. We consider both cases of symmetric as well as asymmetric flip-flops. Symmetric flip-flop leads to a steady…
The electrostatic contribution to spontaneous membrane curvature is calculated within Poisson-Boltzmann theory under a variety of assumptions and emphasizing parameters in the physiological range. Asymmetric surface charges, either fixed…
We present a general theory for the equilibrium structure of cylindrical tubules and helical ribbons of chiral lipid membranes. This theory is based on a continuum elastic free energy that permits variations in the direction of molecular…
Spherical symmetry is ubiquitous in nature. It's therefore unfortunate that spherical system simulations are so hard, and require complete spheres with millions of interacting particles. Here we introduce an approach to model spherical…
By evaporating a drop of lipid dispersion we generate the myelin morphology often seen in dissolving surfactant powders. We explain these puzzling nonequilibrium structures using a geometric argument: The bilayer repeat spacing increases…
A model of lipid bilayers made of a mixture of two lipids with different average compositions on both leaflets, is developed. A Landau hamiltonian describing the lipid-lipid interactions on each leaflet, with two lipidic fields $\psi_1$ and…
We study the general properties of fluid spheres satisfying the heuristic assumption that their areas and proper radius are equal (the Euclidean condition). Dissipative and non-dissipative models are considered. In the latter case, all…
Liquids in oil-bearing porous media assume complex shapes that depend on the reservoir characteristics and the wetting properties of the liquid. The wide variation in the geometry of rock formations makes it difficult to accurately predict…
In Euclidean space, we investigate surfaces whose mean curvature $H$ satisfies the equation $H=\alpha\langle N,\mathbf{x}\rangle+\lambda$, where $N$ is the Gauss map, $\mathbf{x}$ is the position vector and $\alpha$ and $\lambda$ are two…
An analytical theory is developed to describe the dynamics of a closed lipid bilayer membrane (vesicle) freely suspended in a general linear flow. Considering a nearly spherical shape, the solution to the creeping-flow equations is obtained…
Lipid bilayer membranes are not uniform and clusters of lipids in a more ordered state exist within the generally disorder lipid milieu of the membrane. These clusters of ordered lipids microdomains are now referred to as lipid rafts.…
Lipid membranes are abundant in living organisms, where they constitute a surrounding shell for cells and their organelles. There are many circumstances in which the deformations of lipid membranes are involved in living cells: fusion and…
The biological membrane, which compartmentalizes the cell and its organelles, exhibit wide variety of macroscopic shapes of varying morphology and topology. A systematic understanding of the relation of membrane shapes to composition,…
Membrane proteins and lipids can self-assemble into membrane protein polyhedral nanoparticles (MPPNs). MPPNs have a closed spherical surface and a polyhedral protein arrangement, and may offer a new route for structure determination of…