6533b831fe1ef96bd1298e33

RESEARCH PRODUCT

The superlattice model of lateral organization of membranes and its implications on membrane lipid homeostasis.

Jorma A. VirtanenKwan Hon ChengMartin HermanssonPentti Somerharju

subject

Membrane FluidityMembrane lipidsBiophysicsDistributionMolecular dynamicsBiology010402 general chemistry01 natural sciencesBiochemistryModels BiologicalPolar membrane03 medical and health sciencesMembrane LipidsMembrane MicrodomainsMembrane fluidityAnimalsHomeostasisHumansComputer SimulationPhospholipaseLipid bilayer phase behaviorDomain030304 developmental biology0303 health sciencesMembranesMolecular StructureErythrocyte MembraneBiological membraneCell BiologyMembrane transportModels TheoreticalLipid MetabolismLipids0104 chemical sciencesCell biologyErythrocytePhospholipidCholesterolMembraneBiophysicsModelElasticity of cell membranes

description

AbstractMost biological membranes are extremely complex structures consisting of hundreds of different lipid and protein molecules. According to the famous fluid-mosaic model lipids and many proteins are free to diffuse very rapidly in the plane of the membrane. While such fast diffusion implies that different membrane lipids would be laterally randomly distributed, accumulating evidence indicates that in model and natural membranes the lipid components tend to adopt regular (superlattice-like) distributions. The superlattice model, put forward based on such evidence, is intriguing because it predicts that 1) there is a limited number of allowed compositions representing local minima in membrane free energy and 2) those energy minima could provide set-points for enzymes regulating membrane lipid compositions. Furthermore, the existence of a discrete number of allowed compositions could help to maintain organelle identity in the face of rapid inter-organelle membrane traffic.

10.1016/j.bbamem.2008.10.004https://pubmed.ncbi.nlm.nih.gov/19007747