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Journal of Lipid Research, Vol 36, 375-382, Copyright © 1995 by Lipid Research, Inc.
N Noy, DJ Kelleher and AW Scotto
The interactions of retinol with vesicles of dioleoylphosphatidylcholine of
varying radii were studied. The rate constants of dissociation of retinol
from bilayers (k(off)) and the equilibrium partition constants (Keq) of
retinol into bilayers of different sized vesicles were measured. The rate
constants for association of retinol with vesicles were calculated from the
expression Keq = k(on)/k(off). k(off) was 10-fold faster in the smallest
versus the largest vesicles tested. K(on) was also somewhat faster in
vesicles with small radii, but the effect on k(off) was more pronounced,
leading to an overall higher affinity for retinol of bilayers in large
vesicles. The thermodynamic parameters of the dissociation reaction were
studied in vesicles with 0.025, 0.1, and 0.4 microns diameter. The enthalpy
of activation decreased while the entropy of activation of the dissociation
of retinol from bilayers increased as the vesicles become larger. It is
suggested that restructuring of lipid-lipid interactions within the bilayer
play a role in determining the rate by which retinol is solvated off
bilayers. Overall, the data indicate that the rates by which retinol moves
between different cell types in vivo may depend on the geometry of cellular
surfaces.
ARTICLES
Interactions of retinol with lipid bilayers: studies with vesicles of different radii
Division of Nutritional Sciences, Cornell University, Ithaca, NY 14853, USA.
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