Skip to main content
Biophysical Journal logoLink to Biophysical Journal
. 1995 Nov;69(5):1909–1916. doi: 10.1016/S0006-3495(95)80061-5

X-ray diffraction and calorimetric study of N-lignoceryl sphingomyelin membranes.

P R Maulik 1, G G Shipley 1
PMCID: PMC1236424  PMID: 8580334

Abstract

Differential scanning calorimetry and x-ray diffraction have been used to investigate hydrated multibilayers of N-lignoceryl sphingomyelin (C24:0-SM) in the hydration range 0-75 wt % H2O. Anhydrous C24:0-SM exhibits a single endothermic transition at 81.3 degrees C (delta H = 3.6 kcal/mol). At low hydration (12.1 wt % H2O), three different endothermic transitions are observed: low-temperature transition (T1) at 39.4 degrees C (transition enthalpy (delta H1) = 2.8 kcal/mol), intermediate-temperature transition (T2) at 45.5 degrees C, and high-temperature transition (T3) at 51.3 degrees C (combined transition enthalpy (delta H2 + 3) = 5.03 kcal/mol). On increasing hydration, all three transition temperatures of C24:0-SM decrease slightly to reach limiting values of 36.7 degrees C (T1), 44.4 degrees C (T2), and 48.4 degrees C (T3) at approximately 20 wt % H2O. At 22 degrees C (below T1), x-ray diffraction of C24:0-SM at different hydration levels shows two wide-angle reflections, a sharp one at 1/4.2 A-1 and a more diffuse one at 1/4.0 A-1 together with lamellar reflections corresponding to bilayer periodicities increasing from d = 65.4 A to a limiting value of 71.1 A. Electron density profiles show a constant bilayer thickness dp-p approximately 50 A. In contrast, at 40 degrees C (between T1 and T2) a single sharp wide-angle reflection at approximately 1/4.2 A-1 is observed. The lamellar reflections correspond to a larger bilayer periodicity (increasing from d = 69.3-80.2 A) and there is some increase in dp-p (52-56 A) with hydration. These structural parameters,together with calculated lipid thickness and molecular area considerations, suggest that the low temperature endotherm(T1) of hydrated C24:0-SM corresponds to a transition from a tilted, gel state (Gel I) with partially interdigitated chains to an untilted, or less tilted, gel state (Gel 11). At 600C (above T3), the usual liquid-crystalline La bilayer structure (d = 59.5-66.3A; dp p -46 A) is present at all hydrations. Comparison with the behavior of C18:0-SM indicates that the in equivalence of length of the sphingosine (C18) and lignoceryl (C24) chains results in a more complex gel phase polymorphism for the sphingosine (C18) and lignoceryl (C24) chains results in a more complex gel phase polymorphism for C24:0-SM.

Full text

PDF
1910

Selected References

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

  1. Ahmad T. Y., Sparrow J. T., Morrisett J. D. Fluorine-, pyrene-, and nitroxide-labeled sphingomyelin: semi-synthesis and thermotropic properties. J Lipid Res. 1985 Sep;26(9):1160–1165. [PubMed] [Google Scholar]
  2. Barenholz Y., Suurkuusk J., Mountcastle D., Thompson T. E., Biltonen R. L. A calorimetric study of the thermotropic behavior of aqueous dispersions of natural and synthetic sphingomyelins. Biochemistry. 1976 Jun 1;15(11):2441–2447. doi: 10.1021/bi00656a030. [DOI] [PubMed] [Google Scholar]
  3. Braganza L. F., Worcester D. L. Hydrostatic pressure induces hydrocarbon chain interdigitation in single-component phospholipid bilayers. Biochemistry. 1986 May 6;25(9):2591–2596. doi: 10.1021/bi00357a047. [DOI] [PubMed] [Google Scholar]
  4. Bruzik K. S., Tsai M. D. A calorimetric study of the thermotropic behavior of pure sphingomyelin diastereomers. Biochemistry. 1987 Aug 25;26(17):5364–5368. doi: 10.1021/bi00391a022. [DOI] [PubMed] [Google Scholar]
  5. Calhoun W. I., Shipley G. G. Fatty acid composition and thermal behavior of natural sphingomyelins. Biochim Biophys Acta. 1979 Aug 23;555(3):436–441. doi: 10.1016/0005-2736(79)90397-3. [DOI] [PubMed] [Google Scholar]
  6. Calhoun W. I., Shipley G. G. Sphingomyelin--lecithin bilayers and their interaction with cholesterol. Biochemistry. 1979 May 1;18(9):1717–1722. doi: 10.1021/bi00576a013. [DOI] [PubMed] [Google Scholar]
  7. Cohen R., Barenholz Y., Gatt S., Dagan A. Preparation and characterization of well defined D-erythro sphingomyelins. Chem Phys Lipids. 1984 Oct;35(4):371–384. doi: 10.1016/0009-3084(84)90079-3. [DOI] [PubMed] [Google Scholar]
  8. Dong Z., Butcher J. A., Jr An efficient route to N-palmitoyl-D-erythro-sphingomyelin and its 13C-labeled derivatives. Chem Phys Lipids. 1993 Nov;66(1-2):41–46. doi: 10.1016/0009-3084(93)90029-3. [DOI] [PubMed] [Google Scholar]
  9. Fishman P. H., Pacuszka T., Orlandi P. A. Gangliosides as receptors for bacterial enterotoxins. Adv Lipid Res. 1993;25:165–187. [PubMed] [Google Scholar]
  10. Haas N. S., Sripada P. K., Shipley G. G. Effect of chain-linkage on the structure of phosphatidyl choline bilayers. Hydration studies of 1-hexadecyl 2-palmitoyl-sn-glycero-3-phosphocholine. Biophys J. 1990 Jan;57(1):117–124. doi: 10.1016/S0006-3495(90)82512-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Hakomori S. Glycosphingolipids in cellular interaction, differentiation, and oncogenesis. Annu Rev Biochem. 1981;50:733–764. doi: 10.1146/annurev.bi.50.070181.003505. [DOI] [PubMed] [Google Scholar]
  12. Hannun Y. A., Obeid L. M. Ceramide: an intracellular signal for apoptosis. Trends Biochem Sci. 1995 Feb;20(2):73–77. doi: 10.1016/s0968-0004(00)88961-6. [DOI] [PubMed] [Google Scholar]
  13. Hannun Y. A. The sphingomyelin cycle and the second messenger function of ceramide. J Biol Chem. 1994 Feb 4;269(5):3125–3128. [PubMed] [Google Scholar]
  14. Hui S. W., Mason J. T., Huang C. Acyl chain interdigitation in saturated mixed-chain phosphatidylcholine bilayer dispersions. Biochemistry. 1984 Nov 6;23(23):5570–5577. doi: 10.1021/bi00318a029. [DOI] [PubMed] [Google Scholar]
  15. Janiak M. J., Small D. M., Shipley G. G. Temperature and compositional dependence of the structure of hydrated dimyristoyl lecithin. J Biol Chem. 1979 Jul 10;254(13):6068–6078. [PubMed] [Google Scholar]
  16. Kim J. T., Mattai J., Shipley G. G. Gel phase polymorphism in ether-linked dihexadecylphosphatidylcholine bilayers. Biochemistry. 1987 Oct 20;26(21):6592–6598. doi: 10.1021/bi00395a005. [DOI] [PubMed] [Google Scholar]
  17. Levin I. W., Thompson T. E., Barenholz Y., Huang C. Two types of hydrocarbon chain interdigitation in sphingomyelin bilayers. Biochemistry. 1985 Oct 22;24(22):6282–6286. doi: 10.1021/bi00343a036. [DOI] [PubMed] [Google Scholar]
  18. Mattai J., Sripada P. K., Shipley G. G. Mixed-chain phosphatidylcholine bilayers: structure and properties. Biochemistry. 1987 Jun 16;26(12):3287–3297. doi: 10.1021/bi00386a007. [DOI] [PubMed] [Google Scholar]
  19. Maulik P. R., Atkinson D., Shipley G. G. X-ray scattering of vesicles of N-acyl sphingomyelins. Determination of bilayer thickness. Biophys J. 1986 Dec;50(6):1071–1077. doi: 10.1016/S0006-3495(86)83551-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Maulik P. R., Sripada P. K., Shipley G. G. Structure and thermotropic properties of hydrated N-stearoyl sphingomyelin bilayer membranes. Biochim Biophys Acta. 1991 Feb 25;1062(2):211–219. doi: 10.1016/0005-2736(91)90395-o. [DOI] [PubMed] [Google Scholar]
  21. McIntosh T. J., Simon S. A., Ellington J. C., Jr, Porter N. A. New structural model for mixed-chain phosphatidylcholine bilayers. Biochemistry. 1984 Aug 28;23(18):4038–4044. doi: 10.1021/bi00313a005. [DOI] [PubMed] [Google Scholar]
  22. McIntosh T. J., Simon S. A. Hydration force and bilayer deformation: a reevaluation. Biochemistry. 1986 Jul 15;25(14):4058–4066. doi: 10.1021/bi00362a011. [DOI] [PubMed] [Google Scholar]
  23. McIntosh T. J., Simon S. A., Needham D., Huang C. H. Interbilayer interactions between sphingomyelin and sphingomyelin/cholesterol bilayers. Biochemistry. 1992 Feb 25;31(7):2020–2024. doi: 10.1021/bi00122a018. [DOI] [PubMed] [Google Scholar]
  24. McIntosh T. J., Simon S. A., Needham D., Huang C. H. Structure and cohesive properties of sphingomyelin/cholesterol bilayers. Biochemistry. 1992 Feb 25;31(7):2012–2020. doi: 10.1021/bi00122a017. [DOI] [PubMed] [Google Scholar]
  25. Nagle J. F., Wilkinson D. A. Lecithin bilayers. Density measurement and molecular interactions. Biophys J. 1978 Aug;23(2):159–175. doi: 10.1016/S0006-3495(78)85441-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Ranck J. L., Keira T., Luzzati V. A novel packing of the hydrocarbon chains in lipids. The low temperature phases of dipalmitoyl phosphatidyl-glycerol. Biochim Biophys Acta. 1977 Sep 28;488(3):432–441. doi: 10.1016/0005-2760(77)90201-6. [DOI] [PubMed] [Google Scholar]
  27. Ruocco M. J., Siminovitch D. J., Griffin R. G. Comparative study of the gel phases of ether- and ester-linked phosphatidylcholines. Biochemistry. 1985 May 7;24(10):2406–2411. doi: 10.1021/bi00331a003. [DOI] [PubMed] [Google Scholar]
  28. Serrallach E. N., Dijkman R., de Haas G. H., Shipley G. G. Structure and thermotropic properties of 1,3-dipalmitoyl-glycero-2-phosphocholine. J Mol Biol. 1983 Oct 15;170(1):155–174. doi: 10.1016/s0022-2836(83)80231-9. [DOI] [PubMed] [Google Scholar]
  29. Shah J., Sripada P. K., Shipley G. G. Structure and properties of mixed-chain phosphatidylcholine bilayers. Biochemistry. 1990 May 1;29(17):4254–4262. doi: 10.1021/bi00469a030. [DOI] [PubMed] [Google Scholar]
  30. Shipley G. G., Avecilla L. S., Small D. M. Phase behavior and structure of aqueous dispersions of sphingomyelin. J Lipid Res. 1974 Mar;15(2):124–131. [PubMed] [Google Scholar]
  31. Simon S. A., McIntosh T. J. Interdigitated hydrocarbon chain packing causes the biphasic transition behavior in lipid/alcohol suspensions. Biochim Biophys Acta. 1984 Jun 13;773(1):169–172. doi: 10.1016/0005-2736(84)90562-5. [DOI] [PubMed] [Google Scholar]
  32. Sripada P. K., Maulik P. R., Hamilton J. A., Shipley G. G. Partial synthesis and properties of a series of N-acyl sphingomyelins. J Lipid Res. 1987 Jun;28(6):710–718. [PubMed] [Google Scholar]
  33. Tardieu A., Luzzati V., Reman F. C. Structure and polymorphism of the hydrocarbon chains of lipids: a study of lecithin-water phases. J Mol Biol. 1973 Apr 25;75(4):711–733. doi: 10.1016/0022-2836(73)90303-3. [DOI] [PubMed] [Google Scholar]
  34. Torbet J., Wilkins M. H. X-ray diffraction studies of lecithin bilayers. J Theor Biol. 1976 Oct 21;62(2):447–458. doi: 10.1016/0022-5193(76)90129-6. [DOI] [PubMed] [Google Scholar]
  35. Untrach S. H., Shipley G. G. Molecular interactions between lecithin and sphingomyelin. Temperature- and composition-dependent phase separation. J Biol Chem. 1977 Jul 10;252(13):4449–4457. [PubMed] [Google Scholar]
  36. Wiener M. C., Suter R. M., Nagle J. F. Structure of the fully hydrated gel phase of dipalmitoylphosphatidylcholine. Biophys J. 1989 Feb;55(2):315–325. doi: 10.1016/S0006-3495(89)82807-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Worthington C. R., Blaurock A. E. A structural analysis of nerve myelin. Biophys J. 1969 Jul;9(7):970–990. doi: 10.1016/S0006-3495(69)86431-3. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Biophysical Journal are provided here courtesy of The Biophysical Society

RESOURCES