1-2-dielaidoylphosphatidylethanolamine and 1-2-bis(10(2--4--hexadienoyloxy)decanoyl)-sn-glycero-3-phosphocholine

Bennett and O'Brien [(1995) Biochemistry 34, 3102] showed that the ultraviolet light exposure of two-component large unilamellar liposomes (LUV) composed of a 3:1 molar mixture of dioleoylphosphatidylethanolamine (DOPE) and 1,2-bis[10-(2'-hexadienoyloxy)decanoyl]-sn-glycero-3-phosphatidyl- choline (bis-SorbPC) facilitated liposome fusion. The rate and extent of liposome fusion was dependent on the extent of photopolymerization, the temperature, and the pH. Examination of the temperature dependence of fusion of photolyzed and unphotolyzed liposomes demonstrated that an enhancement of the rate of fusion occurred in the temperature range associated with the initial appearance of precursors to the inverted cubic (QII) phase [Barry et al. (1992) Biochemistry 31, 10114]. Here, the effect of the molar lipid ratio of the DOPE/bis-SorbPC liposomes on the temperature for the onset of fusion, i.e. the critical fusion temperature, was characterized by changing the relative amounts of unreactive polymorphic lipid and reactive lamellar lipid. In each case, photopolymerization of bis-SorbPC lowered the critical fusion temperature by ca. 15-20 degrees C. The photoreaction of the bis-SorbPC-containing LUV yields cross-linked poly-SorbPC, enhancing the lateral separation of the DOPE and the polylipid and causing isothermal induction of liposome fusion by lowering the temperature for the onset of fusion. Evidence is presented to support the hypothesis that the critical temperature for fusion of two LUV populations depends on the molar ratio of the monomeric lipids in heterodimers of the two LUV. This analysis indicates that the photopolymerization of appropriately designed LUV can decrease the critical fusion temperature from above to below 37 degrees C.

Topics: 4-Chloro-7-nitrobenzofurazan; Hydrogen-Ion Concentration; Liposomes; Membrane Fusion; Particle Size; Phosphatidylcholines; Phosphatidylethanolamines; Phospholipids; Photochemistry; Scattering, Radiation; Temperature; Ultraviolet Rays

The photopolymerization of two-component large unilamellar liposomes (LUV) composed of 3:1 dioleoylphosphatidylethanolamine (DOPE) and either 1,2-bis[10-(2'-hexadienoyloxy)decanoyl]-sn-glycero-3-phosphatidylc holine (bis-SorbPC) or 1-palmitoyl-2-[10-(2'-hexadienoyloxy)decanoyl]-sn- glycero-3-phosphatidylcholine (mono-SorbPC) facilitated liposome fusion. Fusion was characterized by fluorescent assays for lipid mixing, aqueous contents mixing, and aqueous contents leakage. The rate and extent of the liposome fusion was dependent on the extent of photopolymerization, temperature, and the fusion initiation conditions, including the pH and the presence of Mg2+ ions. Examination of the temperature dependence of fusion for unpolymerized and polymerized liposomes showed that an enhancement of the rate of fusion occurred in the temperature range delta TI, which previous NMR studies have identified as the initial appearance of precursors to the formation of the inverted cubic phase [Barry, J. A., et al. (1992) Biochemistry 31, 10114]. The phase behavior and fusion characteristics of the DOPE/bis-SorbPC (3:1) membranes provide unequivocal evidence that liposome fusion is mediated via intermediates associated with the lamellar to QII phase transition rather than the HII phase. Photopolymerization of SorbPC-containing liposomes forms poly-SorbPC, which enhances the lateral separation of the liposome components. The formation of enriched domains of polymorphic lipids, e.g., DOPE, causes isothermal induction of fusion by lowering the critical fusion temperature of the membranes.

Topics: Kinetics; Liposomes; Membrane Fusion; Phosphatidylcholines; Phosphatidylethanolamines; Photochemistry; Polymers; Spectrometry, Fluorescence; Temperature

It was recently shown that oligolamellar vesicles of 3:1 mixtures of dioleoylphosphatidylethanolamine (DOPE) and the photopolymerizable lipid 1,2-bis[10-(2',4'-hexadienoyloxy)decanoyl]-sn-glycero-3-phosphocho line (SorbPC) are destabilized by polymerization of the SorbPC [Lamparski, H., Liman, U., Frankel, D.A., Barry, J.A., Ramaswami, V., Brown, M.F., & O'Brien, D.F. (1992) Biochemistry 31, 685-694]. The current work describes the polymorphic phase behavior of these mixtures in extended bilayers, as studied by 31P NMR spectroscopy and X-ray diffraction. In the NMR experiments, samples with varying degrees of polymerization were slowly raised in temperature, with spectra acquired every 2.5-10 degrees C. In the unpolymerized mixiture, and in those photopolymerized samples where the monomeric SorbPC was decreased by 33% and 51%, an isotropic signal grew progressively until no signal from the lamellar liquid-crystalline (L alpha) phase remained. In the highly polymerized sample with a 90% loss of monomeric SorbPC, less than 20% of the lipids underwent this transition. In none of the samples was an inverted hexagonal phase (HII) observed, under conditions of slow heating to almost 100 degrees C. The X-ray diffraction studies indicated that samples which exhibit the isotropic NMR signal corresponded to a structure exhibiting no well-defined crystalline order, which upon thermal cycling became an inverted cubic phase belonging to either the Pn3m or Pn3 space groups. The temperature of the transition to the cubic precursor decreased as the extent of polymerization increased, demonstrating that photopolymerization of these lipid bilayers can significantly alter the composition and thermotropic phase behavior of the mixture.

Topics: Crystallization; Lipids; Liposomes; Magnetic Resonance Spectroscopy; Phosphatidylcholines; Phosphatidylethanolamines; Photochemistry; Polymers; Temperature; X-Ray Diffraction