Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1986 Oct;83(19):7132–7136. doi: 10.1073/pnas.83.19.7132

Thermal-mechanical fluctuations enhance repulsion between bimolecular layers.

E A Evans, V A Parsegian
PMCID: PMC386669  PMID: 3463955

Abstract

Beginning with the free energy potential for long-range interactions between parallel flat sheets and the mechanical energy of bending those sheets, we have derived an upper bound for repulsion enhanced by thermal undulations of sheets in a multilamellar array. Through a self-consistent (mean-field) potential, we cover the full range of layer separations from close-in to far-apart, where the enhanced repulsion approaches the weak steric interaction derived previously by Helfrich [Helfrich, W. (1978) Z. Naturforsch. 33a, 305-315]. We have examined the effect of the fluctuation-enhanced repulsion in experimental studies of osmotic (and mechanical) compression of multilamellar lipid arrays, mechanical compression of bilayers immobilized on mica substrates, and controlled adhesion of giant bilayer membrane vesicles.

Full text

PDF
7132

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Cowley A. C., Fuller N. L., Rand R. P., Parsegian V. A. Measurement of repulsive forces between charged phospholipid bilayers. Biochemistry. 1978 Jul 25;17(15):3163–3168. doi: 10.1021/bi00608a034. [DOI] [PubMed] [Google Scholar]
  2. Evans E. A. Bending resistance and chemically induced moments in membrane bilayers. Biophys J. 1974 Dec;14(12):923–931. doi: 10.1016/S0006-3495(74)85959-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Evans E. A., Parsegian V. A. Energetics of membrane deformation and adhesion in cell and vesicle aggregation. Ann N Y Acad Sci. 1983;416:13–33. doi: 10.1111/j.1749-6632.1983.tb35176.x. [DOI] [PubMed] [Google Scholar]
  4. Evans E., Metcalfe M. Free energy potential for aggregation of giant, neutral lipid bilayer vesicles by Van der Waals attraction. Biophys J. 1984 Sep;46(3):423–426. doi: 10.1016/S0006-3495(84)84039-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Inoko Y., Yamaguchi T., Furuya K., Mitsui T. Effects of cations on dipalmitoyl phosphatidylcholine/cholesterol/water systems. Biochim Biophys Acta. 1975 Nov 17;413(1):24–32. doi: 10.1016/0005-2736(75)90055-3. [DOI] [PubMed] [Google Scholar]
  6. LeNeveu D. M., Rand R. P. Measurement and modification of forces between lecithin bilayers. Biophys J. 1977 May;18(2):209–230. doi: 10.1016/S0006-3495(77)85608-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. LeNeveu D. M., Rand R. P., Parsegian V. A. Measurement of forces between lecithin bilayers. Nature. 1976 Feb 19;259(5544):601–603. doi: 10.1038/259601a0. [DOI] [PubMed] [Google Scholar]
  8. Lis L. J., Lis W. T., Parsegian V. A., Rand R. P. Adsorption of divalent cations to a variety of phosphatidylcholine bilayers. Biochemistry. 1981 Mar 31;20(7):1771–1777. doi: 10.1021/bi00510a010. [DOI] [PubMed] [Google Scholar]
  9. Lis L. J., McAlister M., Fuller N., Rand R. P., Parsegian V. A. Interactions between neutral phospholipid bilayer membranes. Biophys J. 1982 Mar;37(3):657–665. [PMC free article] [PubMed] [Google Scholar]
  10. Lis L. J., Parsegian V. A., Rand R. P. Binding of divalent cations of dipalmitoylphosphatidylcholine bilayers and its effect on bilayer interaction. Biochemistry. 1981 Mar 31;20(7):1761–1770. doi: 10.1021/bi00510a009. [DOI] [PubMed] [Google Scholar]
  11. Loosley-Millman M. E., Rand R. P., Parsegian V. A. Effects of monovalent ion binding and screening on measured electrostatic forces between charged phospholipid bilayers. Biophys J. 1982 Dec;40(3):221–232. doi: 10.1016/S0006-3495(82)84477-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Marra J., Israelachvili J. Direct measurements of forces between phosphatidylcholine and phosphatidylethanolamine bilayers in aqueous electrolyte solutions. Biochemistry. 1985 Aug 13;24(17):4608–4618. doi: 10.1021/bi00338a020. [DOI] [PubMed] [Google Scholar]
  13. McLaughlin S., Mulrine N., Gresalfi T., Vaio G., McLaughlin A. Adsorption of divalent cations to bilayer membranes containing phosphatidylserine. J Gen Physiol. 1981 Apr;77(4):445–473. doi: 10.1085/jgp.77.4.445. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Parsegian V. A., Fuller N., Rand R. P. Measured work of deformation and repulsion of lecithin bilayers. Proc Natl Acad Sci U S A. 1979 Jun;76(6):2750–2754. doi: 10.1073/pnas.76.6.2750. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Rand R. P. Interacting phospholipid bilayers: measured forces and induced structural changes. Annu Rev Biophys Bioeng. 1981;10:277–314. doi: 10.1146/annurev.bb.10.060181.001425. [DOI] [PubMed] [Google Scholar]
  16. Schneider M. B., Jenkins J. T., Webb W. W. Thermal fluctuations of large cylindrical phospholipid vesicles. Biophys J. 1984 May;45(5):891–899. doi: 10.1016/S0006-3495(84)84235-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Servuss R. M., Harbich W., Helfrich W. Measurement of the curvature-elastic modulus of egg lecithin bilayers. Biochim Biophys Acta. 1976 Jul 15;436(4):900–903. doi: 10.1016/0005-2736(76)90422-3. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES