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Comparative calorimetric and spectroscopic studies of the effects of lanosterol and cholesterol on the thermotropic phase behavior and organization of dipalmitoylphosphatidylcholine bilayer membranes
Authors:Mannock David A  Lewis Ruthven N A H  McElhaney Ronald N
Institution:Department of Biochemistry, University of Alberta, Edmonton, Alberta, Canada
Abstract:We carried out comparative DSC and Fourier transform infrared spectroscopic studies of the effects of cholesterol and lanosterol on the thermotropic phase behavior and organization of DPPC bilayers. Lanosterol is the biosynthetic precursor of cholesterol and differs in having three rather than two axial methyl groups projecting from the β-face of the planar steroid ring system and one axial methyl group projecting from the α-face, whereas cholesterol has none. Our DSC studies indicate that the incorporation of lanosterol is more effective than cholesterol is in reducing the enthalpy of the pretransition. Lanosterol is also initially more effective than cholesterol in reducing the enthalpies of both the sharp and broad components of the main phase transition. However, at sterol concentrations of 50 mol %, lanosterol does not abolish the cooperative hydrocarbon chain-melting phase transition as does cholesterol. Moreover, at higher lanosterol concentrations (~30–50 mol %), both sharp and broad low-temperature endotherms appear in the DSC heating scans, suggestive of the formation of lanosterol crystallites, and of the lateral phase separation of lanosterol-enriched phospholipid domains, respectively, at low temperatures, whereas such behavior is not observed with cholesterol at comparable concentrations. Our Fourier transform infrared spectroscopic studies demonstrate that lanosterol incorporation produces a less tightly packed bilayer than does cholesterol, which is characterized by increased hydration in the glycerol backbone region of the DPPC bilayer. These and other results indicate that lanosterol is less miscible in DPPC bilayers than is cholesterol, but perturbs their organization to a greater extent, probably due primarily to the rougher faces and larger cross-sectional area of the lanosterol molecule and perhaps secondarily to its decreased ability to form hydrogen bonds with adjacent DPPC molecules. Nevertheless, lanosterol does appear to produce a lamellar liquid-ordered phase in DPPC bilayers, although this phase is not as tightly packed as comparable cholesterol/DPPC mixtures.
Keywords:DSC  differential scanning calorimetry  DPPC  dipalmitoylphosphatidylcholine  PC  phosphatidylcholine  DMPC  dimyristoylphosphatidylcholine  DOPC  dioleoylphosphatidylcholine  PPetPC  1-palmitoyl-2-petroselinoylphosphatidylcholine  SpM  sphingomyelin  FTIR  Fourier transform infrared  NMR  nuclear magnetic resonance  Tp  the pretransition temperature maximum  Tm  the main transition temperature maximum  ΔH  the transition enthalpy  ΔT½  the width of the phase transition at half height  inversely related to the cooperativity of the phase transition  Lβ and Lβ  lamellar gel phases with tilted and untilted hydrocarbon chains  respectively  Pβ  rippled gel phase with tilted hydrocarbon chains  Lα or Ld  lamellar liquid-crystalline or liquid-disordered phase  Lo  lamellar liquid-ordered phase  BC1 and BC2  first and second broad endotherm components of the lanosterol-DPPC DSC thermograms
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