Membrane bending energy and shape determination of phospholipid vesicles and red blood cells
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Abstract
A procedure is developed to calculate red blood cell and phospholipid vesicle shapes within the bilayer couple model of the membrane. The membrane is assumed to consist of two laterally incompressible leaflets which are in close contact but unconnected. Shapes are determined by minimizing the membrane bending energy at a given volume of a cell (V), given average membrane area (A) and given difference of the areas of two leaflets (ΔA). Different classes of shapes exist in parts of the v/Δa phase diagram, where v and Δa are the volume and the leaflet area difference relative to the sphere with area A. The limiting shapes are composed of sections of spheres with only two values allowed for their radii. Two low energy axisymmetrical classes, which include discocyte and stomatocyte shapes are studied and their phase diagrams are analyzed. For v=0.6, the discocyte is the lowest energy shape, which transforms by decreasing Δa continuously into a stomatocyte. The spontaneous membrane curvature (C0) and compressibility of membrane leaflest can be incorporated into the model.
A model, where ΔA is free and C0 determines the shapes at given V and A, is also studied. In this case, by decreasing C0, a discocyte transforms discontinuously into an almost closed stomatocyte.
Key words
Phospholipid membrane red blood cell shapes membrane bending energyPreview
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References
- Beck JS (1978) Relations between membrane monolayers in some red cell shape transformations. J Theor Biol 75:487–501Google Scholar
- Bütikofer P, Brodbeck U, Ott P (1987) Modulation of erythrocyte vesiculation by amphiphilic drugs. Biochim Biophys Acta 901:291–295Google Scholar
- Canham PB (1970) The minimum energy of bending as a possible explanation of the biconcave shape of the human red blood cell. J Theor Biol 26:61–81Google Scholar
- Deuling HJ, Helfrich W (1976a) The curvature elasticity of fluid membranes: A catalogue of vesicle shapes. J Phys (Paris) 37:1335–1345Google Scholar
- Deuling HJ, Helfrich W (1976b) Red blood cell shapes as explained on the basis of curvature elasticity. Biophys J 16:861–868Google Scholar
- Deuticke B (1968) Transformation and restoration of biconcave shape of human erythrocytes induced by amphiphilic agents and changes of ionic environment. Biochim Biophys Acta 163:494–500Google Scholar
- Evans EA (1974) Bending resistance and chemically induced moments in membrane bilayers. Biophys J 14:923–931Google Scholar
- Evans EA (1980) Minimum energy analysis of membrane deformation applied to pipet aspiration and surface adhesion of red blood cells. Biophys J 30:265–284Google Scholar
- Evans EA, Skalak R (1980) Mechanics and thermodynamics of biomembranes. CRC Press, Boca Raton, FLGoogle Scholar
- Helfrich W, Deuling HJ (1975) Some theoretical shapes of red blood cells. J. Phys (Paris) Colloq 36:327–329Google Scholar
- Hochmuth RM, Waugh RE (1987) Erythrocyte membrane elasticity and viscosity. Annu Rev Physiol 49:209–219Google Scholar
- Jenkins JT (1977) Static equilibrium configurations of a model red blood cell. J Math Biol 4:149–169Google Scholar
- Luke JC (1982) A method for the calculation of vesicle shapes. SIAM J Appl Math 42:333–345Google Scholar
- Luke JC, Kaplan JI (1979) On theoretical shapes of bilipid vesicles under conditions of increasing membrane area. Biophys J 25:107–111Google Scholar
- Peterson MA (1985) An instability of the red blood cell shape. J Appl Phys 57:1739–1742Google Scholar
- Sackmann E, Duwe H-P, Engelhardt H (1986) Membrane bending elasticity and its role for shape fluctuations and shape transformations of cells and vesicles. Faraday Discuss Chem Soc 81:281–294Google Scholar
- Sheetz MP, Singer SJ (1974) Biological membranes as bilayer couples. A mechanism of drug-erythrocyte interactions. Proc Natl Acad Sci USA 72:4457–4461Google Scholar
- Svetina S, Žekš B (1983) Bilayer couple hypothesis of red cell shape transformations and osmotic hemolysis. Biomed Biochim Acta 42:86–90Google Scholar
- Svetina S, Žekš B (1984) Red cell membrane properties and the bilayer couple hypothesis of red cell shape transformations. In: Tomicki B, Kuczera J, Przestalski S (eds) Biophysics of membrane transport, part II. Agricultural University Wroclaw, pp 107–126Google Scholar
- Svetina S, Žekš B (1985) Bilayer couple as a possible mechanism of biological shape formation. Biomed Biochim Acta 44: 979–986Google Scholar
- Svetina S, Ottova-Leitmannova A, Glaser R (1982) Membrane bending energy in relation to bilayer couples concept of red blood cell shape transformations. J Theor Biol 94:13–23Google Scholar
- Svetina S, Brumen M, Žekš B (1985) Lipid bilayer elasticity and the bilayer couple interpretation of red cell shape transformations and lysis. Stud Biophys 110:177–184Google Scholar
- Svetina S, Brumen M, Žekš B (1988) The role of the membrane elastic properties and cell volume in the formation of red blood cell shapes. In: Benga Gh, Tager JM (eds) Biomembranes: basic and medical research. Springer, Berlin Heidelberg New York, pp 177–187Google Scholar
- Zarda PR, Chien S, Skalak R (1977) Elastic deformations of red blood cells. J Biomech 10:211–221Google Scholar