N-Palmitoyl Sphingomyelin Bilayers:  Structure and Interactions with Cholesterol and Dipalmitoylphosphatidylcholine

• Published in: Biochemistry (Easton) 1996-06, Vol.35 (24), p.8025-8034
• Main Authors: Maulik, P. R, Shipley, G. G
• Format: Article
• Language: English
• Subjects: 1,2-Dipalmitoylphosphatidylcholine - chemistry; Calorimetry, Differential Scanning; Cholesterol - chemistry; Lipid Bilayers; Models, Structural; Periodicity; Sphingomyelins - chemistry; Thermodynamics; X-Ray Diffraction
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi9528356

The structure and thermotropic properties of N-palmitoyl sphingomyelin (C16:0-SM) and its interaction with cholesterol and dipalmitoylphosphatidylcholine (DPPC) have been studied by differential scanning calorimetry (DSC) and X-ray diffraction methods. DSC of hydrated multi-bilayers of C16:0-SM shows reversible chain-melting transitions. On heating, anhydrous C16:0-SM exhibits an endothermic transition at 75 °C (ΔH = 4.0 kcal/mol). Increasing hydration progressively lowers the transition temperature (T M) and increases the transition enthalpy (ΔH), until limiting values (T M = 41 °C, ΔH = 7.5 kcal/mol) are observed for hydration values >25 wt % H2O. X-ray diffraction at temperatures below (29 °C) T M show a bilayer gel structure (d = 73.5 Å, sharp 4.2 Å reflection) for C16:0-SM at full hydration; above T M, at 55 °C, a bilayer liquid-crystal phase is present (d = 66.6 Å, diffuse 4.6 Å reflection). Addition of cholesterol to C16:0-SM bilayers results in a progressive decrease in the enthalpy of the transition at 41 °C, and no cooperative transition is detected at >50 mol % cholesterol. X-ray diffraction shows no difference in the bilayer periodicity, position/width of the wide-angle reflections, or electron density profiles at 29 and 55 °C when 50 mol % cholesterol is present. Thus, cholesterol inserts into C16:0-SM bilayers progressively removing the chain-melting transition and changing the structural characteristics of the bilayer. DSC and X-ray diffraction data show that DPPC is completely miscible with C16:0-SM bilayers in both the gel and liquid-crystalline phases; however, 30 mol % C16:0-SM removes the pre-transition exhibited by DPPC.