Short-range interactions between lipid bilayers measured by X-ray diffraction

Current Opinion in Structural Biology

Volumn 10, Issue 4, 2000, Pages 481-485

  McIntosh, Thomas J ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOLIPID; MEMBRANE PHOSPHOLIPID;

FORCE; HUMAN; LIPID BILAYER; MOLECULAR INTERACTION; NONHUMAN; OSMOTIC PRESSURE; PRIORITY JOURNAL; REVIEW; X RAY DIFFRACTION;

EID: 0033944497     PISSN: 0959440X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0959-440X(00)00118-4     Document Type: Review

References (58)

1. Marra J., Israelachvili J. Direct measurements of forces between phosphatidylcholine and phosphatidylethanolamine bilayers in aqueous electrolyte solutions. Biochemistry. 24:1985;4608-4618.
2. Israelachvili J., Marra J. Direct methods for measuring conformational forces (hydration forces) between membrane and other surfaces. Methods Enzymol. 127:1986;353-361.
3. LeNeveu D.M., Rand R.P., Parsegian V.A., Gingell D. Measurement and modification of forces between lecithin bilayers. Biophys J. 18:1977;209-230.
4. Parsegian V.A., Fuller N., Rand R.P. Measured work of deformation and repulsion of lecithin bilayers. Proc Natl Acad Sci USA. 76:1979;2750-2754.
5. McIntosh T.J., Simon S.A. The hydration force and bilayer deformation: a reevaluation. Biochemistry. 25:1986;4058-4066.
6. McIntosh T.J., Magid A.D., Simon S.A. Steric repulsion between phosphatidylcholine bilayers. Biochemistry. 26:1987;7325-7332.
7. Rand R.P., Parsegian V.A. Hydration forces between phospholipid bilayers. Biochim Biophys Acta. 988:1989;351-376.
8. Parsegian V.A., Rand R.P. On molecular protrusion as the source of hydration forces. Langmuir. 7:1991;1299-1301.
9. Lipowsky R., Grotehans S. Hydration vs. protrusion forces between lipid bilayers. Europhys Lett. 23:1993;599-604.
10. McIntosh T.J., Simon S.A. Hydration and steric pressures between phospholipid bilayers. Annu Rev Biophys Biomol Struct. 23:1994;27-51.
11. Israelachvili J., Wennerstrom H. Role of hydration and water structure in biological and colloidal interactions. Nature. 379:1996;219-225.
12. Marcelja S., Radic N. Repulsion of interfaces due to boundary water. Chem Phys Lett. 42:1976;129-130.
13. Gruen D.W.R., Marcelja S. Spatially varying polarization in water. J Chem Soc Faraday Trans 2. 79:1983;225-242.
14. Kornyshev A.A. On the non-local electrostatic theory of hydration force. J Electroanal Chem. 204:1986;79-84.
15. Leikin S., Parsegian V.A., Rau D.C. Hydration forces. Annu Rev Phys Chem. 44:1993;369-395.
16. McIntosh T.J., Simon S.A. Contribution of hydration and steric (entropic) pressures to the interaction between phosphatidylcholine bilayers: experiments with the subgel phase. Biochemistry. 32:1993;8374-8384.
17. Israelachvili J.N., Wennerstrom H. Hydration or steric forces between amphiphilic surfaces? Langmuir. 6:1990;873-876.
18. Israelachvili J.N., Wennerstrom H. Entropic forces between amphiphilic surfaces in liquids. J Phys Chem. 96:1992;520-531.
19. Harbich W., Helfrich W. The swelling of egg lecithin in water. Chem Phys Lipids. 36:1984;39-63.
20. Helfrich W., Servuss R-M. Undulations, steric interactions and cohesion of fluid membranes. Il Nuovo Cimento. 3:1984;137-151.
21. Evans E.A., Parsegian V.A. Thermal-mechanical fluctuations enhance repulsion between bimolecular layers. Proc Natl Acad Sci USA. 83:1986;7132-7136.
22. Safinya C.R. Rigid and fluctuating surfaces: a series of synchrotron X-ray scattering studies of interacting stacked membranes. Riste T., Sherrington D. Phase Transitions in Soft Condensed Matter. 1989;249-270 Plenum Publishing Corp, New York.
23. McIntosh T.J., Magid A.D., Simon S.A. Repulsive interactions between uncharged bilayers. Hydration and fluctuation pressures for monoglycerides. Biophys J. 55:1989;897-904.
24. Evans E. Entropy-driven tension in vesicle membranes and unbinding of adherent vesicles. Langmuir. 7:1991;1900-1908.
25. McIntosh T.J., Advani S., Burton R.E., Zhelev D.V., Needham D., Simon S.A. Experimental tests for protrusion and undulation pressures in phospholipid bilayers. Biochemistry. 34:1995;8520-8532.
26. Curatolo W. Glycolipid function. Biochim Biophys Acta. 906:1987;137-160.
27. Kojima N., Hakomori S-I. Specific interaction between gangliotriaosylceramide and sialosyllactosylceramide as a basis for specific cellular recognition between lymphoma and melanoma cells. J Biol Chem. 264:1989;20 159-20 162.
28. Vogel J., Bendas G., Bakowsky U., Hummel G., Schmidt R.R., Kettman U., Rothe U. The role of glycolipids in mediating cell adhesion: a flow chamber study. Biochim Biophys Acta. 1372:1998;205-215.
29. Parker J.L. Forces between bilayers containing charged glycolipids. J Colloid Interface Sci. 137:1990;571-576.
30. Luckham P., Wood J., Swart R. The surface properties of gangliosides. II. Direct measurement of the interaction between bilayers deposited on mica sheets. J Colloid Interface Sci. 156:1993;173-183.
31. McIntosh T.J., Simon S.A. Long- and short-range interactions between phospholipid/ganglioside GM1 bilayers. Biochemistry. 33:1994;10 477-10 486.
32. Bosio A., Binczek E., Haupt W.F., Stoffel W. Composition and biophysical properties of myelin lipid define the neurological defects in galactocerebroside- and sulfatide-deficient mice. J Neurochem. 70:1998;308-315.
33. Dupree J., Coetzee T., Blight A., Suzuki K., Popko B. Myelin galactolipids are essential for proper node of Ranvier formation in the CNS. J Neurosci. 18:1998;1642-1649.
34. Ruocco M.J., Atkinson D., Small D.M., Skarjune R.P., Oldfield E., Shipley G.G. X-ray diffraction and calorimetric study of anhydrous and hydrated N-palmitoylgalactosylsphingosine (cerebroside). Biochemistry. 21:1981;5957-5966.
35. Ruocco M.J., Shipley G.G. Hydration of N-palmitoylgalactosylsphingosine compared to monosaccharide hydration. Biochim Biophys Acta. 735:1983;305-308.
36. Shah J., Atienza J.M., Rawlings A.V., Shipley G.G. Physical properties of ceramides: effect of fatty acid hydroxylation. J Lipid Res. 36:1995;1945-1955.
37. Shah J., Atienza J.M., Duclos R.I., Rawlings A.V., Dong Z., Shipley G.G. Structural and thermotropic properties of synthetic C16:0 (palmitoyl) ceramide: effect of hydration. J Lipid Res. 36:1995;1936-1944.
38. Haas N.S., Shipley G.G. Structure and properties of N-palmitoleoylgalactosylsphingosine (ceramide). Biochim Biophys Acta. 1240:1995;133-141.
39. Petrache H.I., Gouliaev N., Tristram-Nagle S., Zhang R., Suter R.M., Nagle J.F. Interbilayer interactions: high resolution X-ray study. Phys Rev E. 57:1998;7014-7024. This paper uses X-ray diffraction to analyze liquid-crystalline phase bilayers composed of three different lipids. The authors use osmotic stress experiments to obtain both pressure/distance relations and measurements of interbilayer water spacing fluctuations. The data are decomposed to provide values for the magnitude and decay lengths of both the hydration and the undulation pressures.
40. Petrache H.I., Tristram-Nagle S., Nagle J.F. Fluid phase structure of EPC and DMPC bilayers. Chem Phys Lipids. 95:1998;83-94.
41. Tristram-Nagle S., Petrache H.I., Nagle J.F. Structure and interactions of fully hydrated dioleoylphosphatidylcholine bilayers. Biophys J. 75:1998;917-925. This study uses osmotic stress/X-ray diffraction data to show that the undulation pressure decays exponentially with increasing bilayer separation, in agreement with theoretical treatments for soft confinement.
42. Zhang R., Tristram-Nagle S., Sun W., Headrick R.L., Irving T.C., Suter R.M., Nagle J.F. Small-angle x-ray scattering from lipid bilayers is well described by modified Caile theory but not by paracrystalline theory. Biophys J. 70:1996;349-357.
43. Hristova K., White S.H. Determination of the hydrocarbon core structure of fluid dioleoylphosphocholine (DOPC) bilayers by X-ray diffraction using specific bromination of the double bonds: effect of hydration. Biophys J. 74:1998;2419-2433.
44. Podgornik R., Parsegian V.A. Thermal-mechanical fluctuations of fluid membranes in confined geometries: the case of soft confinement. Langmuir. 8:1992;557-562.
45. Gouliaev N., Nagle J.F. Simulations of interacting membranes in the soft confinement regime. Phys Rev Lett. 81:1998;2610-2613.
46. Simon S.A., Advani S., McIntosh T.J. Temperature dependence of the repulsive pressure between phosphatidylcholine bilayers. Biophys J. 69:1995;1473-1483.
47. Katsaras J. Adsorbed to a rigid substrate, dimyristoylphosphatidylcholine multilayers attain full hydration in all mesophases. Biophys J. 75:1998;2157-2162. This paper demonstrates that a novel specimen holder can be used to study oriented multilamellar bilayers that, at 100% relative humidity, have the same repeat periods as unoriented lipid dispersions.
48. •] to show that there is no 'vapor pressure paradox'. Similar pressure/distance relations are obtained when either unoriented liposomes or multibilayers oriented on a solid substrate are squeezed together by polymer solutions.
49. Podgornik R., Parsegian V.A. On a possible microscopic mechanism underlying the vapor pressure paradox. Biophys J. 72:1997;942-952.
50. Vogel M., Munster C., Fenz W., Salditt T. Thermal unbinding of highly oriented phospholipid membranes. Phys Rev Lett. 84:2000;390-393.
51. Binder H., Gutberlet T., Anikin A., Klose G. Hydration of the dienic lipid dioctacadienoylphosphatidylcholine in the lamellar phase - an infrared linear dichroism and X-ray study on headgroup orientation, water ordering, and bilayer dimensions. Biophys J. 74:1998;1908-1923.
52. Binder H., Dietrich U., Schalke M., Pfeiffer H. Hydration-induced deformation of lipid aggregates before and after polymerisation. Langmuir. 15:1999;4857-4866.
53. McIntosh T.J., Magid A.D., Simon S.A. Cholesterol modifies the short-range repulsive interactions between phosphatidylcholine membranes. Biochemistry. 28:1989;17-25.
54. Snyder S., Kim D., McIntosh T.J. Lipopolysaccharide bilayer structure: effect of chemotype, core mutations, divalent cations, and temperature. Biochemistry. 38:1999;10 758-10 767. Osmotic pressure/X-ray diffraction experiments were used to obtain pressure/distance relations and structures for the complex glycolipid (LPS; lipopolysaccharide) found on the outer surface of Gram-negative bacteria. In the absence of divalent cations, there is a strong repulsive interaction caused by the negative charge on the LPS. In the presence of divalent cations, however, the charge is neutralized and apposing LPS bilayers strongly adhere.
55. Kulkarni K., Snyder D.S., McIntosh T.J. Adhesion between cerebroside bilayers. Biochemistry. 38:1999;15 264-15 721. The methods developed in [56] were used to obtain the adhesive energy between cerebroside (galactosylceramide) bilayers. The adhesive energy for ceramide bilayers is much stronger than for typical phospholipid bilayers, indicating a strong adhesive force between these glycolipids.
56. McIntosh T.J., Simon S.A. Adhesion between phosphatidylethanolamine bilayers. Langmuir. 12:1996;1622-1630.
57. Yu Z.W., Calvert T.L., Leckband D. Molecular forces between membranes displaying neutral glycosphingolipids: evidence for carbohydrate attraction. Biochemistry. 37:1998;1540-1550.
58. Saxena K., Duclos R.I., Zimmerman P., Scmidt R.R., Shipley G.G. Structure and properties of totally synthetic galacto- and gluco-cerebrosides. J Lipid Res. 40:1999;839-849.