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(Received for publication, February 12, 1996, and in revised form, April 8, 1996)
From the Faculty of Pharmaceutical Sciences, Kyoto University,
Sakyo-ku, Kyoto 606-01, Japan
Plasma triglyceride-rich lipoproteins vary in
lipid composition during their metabolism. We investigated the effects
of the lipid composition of emulsion particles, specifically those of
cholesterol enrichment and core replacement (replacing core
triglyceride with cholesteryl oleate), on the physical states of
surface and core lipids. Steady-state and time-resolved fluorescence
anisotropies were measured in lipid emulsions using
1,6-diphenylhexatriene to probe the core and 1,6-diphenylhexatriene
analogues for the outer and inner hydrophobic portions of surface
phospholipids. In the absence of cholesterol, core replacement had
little effect on the surface rigidity, despite the large difference in
core mobility. However, core replacement caused a marked increase in
surface rigidity in the presence of cholesterol. Quenching experiments
using the fluorescent cholesterol analogue, dehydroergosterol,
indicated that core replacement allowed surface dehydroergosterol to
redistribute from the inner to the outer regions in the emulsion
surface. These results indicated that core replacement modulates the
surface properties of the emulsion particles through the redistribution
of cholesterol in the surface layers. Furthermore, core replacement
significantly decreased the binding of apolipoprotein E to the emulsion
surface, whereas the binding of apolipoprotein CII responded to the
cholesterol enrichment. This binding behavior of exchangeable
apolipoproteins may closely correlate with the location of surface
cholesterol and the mobility of core lipids.
Volume 271, Number 26,
Issue of June 28, 1996
pp. 15515-15520
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
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