G. Degovics et al., STRUCTURE AND THERMOTROPIC BEHAVIOR OF MIXED CHOLINE PHOSPHOLIPID MODEL MEMBRANES, Journal of applied crystallography, 30(2), 1997, pp. 776-780
Phosphatidylcholines and sphingomyelins are among the most abundant li
pids in mammalian cell membranes, being major components of platelets
or erythrocytes, and of the lipid monolayer of lipoproteins. General e
fforts have been devoted to the elucidation of the interaction of the
ubiquitous membrane component cholesterol with these choline phospholi
pids, but fewer studies have been reported on the interaction between
the phospholipids themselves. A gel to liquid-crystalline phase transi
tion was observed for pure sphingomyelin liposomes at physiological te
mperature, while palmitoyloleoyl phosphatidylcholine adopts a liquid-c
rystalline phase in the temperature range 273-323 K. The two phospholi
pids are miscible at all molar ratios in the liquid-crystalline phase,
characterized by very similar lamellar repeat distances for all binar
y lipid mixtures. The gel phase of pure sphingolipid liposomes exhibit
ed a markedly smaller lamellar repeat distance as compared to mixed li
pid vesicles, which increased slightly with temperature for the pure s
phingomyelin (66.9-69.2 Angstrom). Concomitantly, altered hydrocarbon
chain packing was observed. Similar diffractograms were obtained in th
e presence of 10 mol% phosphatidylcholine. However, in the composition
range between 20 and 60 mol% phosphatidylcholine in the phosphatidylc
holine-sphingomyelin admixture, the lamellar repeat distance in the ge
l phase was markedly increased and remained almost constant (around 75
Angstrom) below the phase transition.