E. Hayakawa et al., ALTERED MOLECULAR-MOTION IN PHOSPHOLIPID HEADGROUPS DURING L-ALPHA-H-II TRANSITION INDUCED BY CHOLESTEROL, Biomedical research, 18(6), 1997, pp. 453-460
Cholesterol is highly concentrated in the synaptic membranes which und
ergo frequent membrane fusion and is believed to play an important rol
e in the lipid phase transition that accompanies fusion. To better und
erstand the phosholipid phase transition and associated molecular moti
on of phospholipids during the lamellar to inverted hexagonal transiti
on, two major methods were used. First, sn-1,2-dioleoylglycerol was ad
ded to synthetic vesicles, and inverted hexagonal formation was detect
ed using P-31-NMR. Multilamellar sheets were composed of 1,2-dioleoyl-
3-sn-phosphatidylcholine, 1,2-dioleoyl-3-sn-phosphatidylethanolamine a
nd cholesterol (1:1:1 in molar ratio) and 5 mol%-sn-1,2-dioleoylglycer
ol was added to transform lamellar to inverted hexagonal structures. H
owever, the transition also required cholesterol. Multilamellar vesicl
es were composed of phosphatidylcholine, phosphatidylethanolamine and
cholesterol and were investigated using a time-resolved fluorescence d
epolarization method with dansyl-phosphatidylethanolamine as a fluores
cent probe. The molecular motion of phospholipid headgroups decreased
during the lamellar to inverted hexagonal phase transition, suggesting
that the headgroups of phospholipid molecules are more tightly packed
in inverted hexagonal structure than in lamellar form of membrane.