Ch. Chen et al., THERMODYNAMIC AND FLUORESCENCE STUDIES OF THE UNDERLYING FACTORS IN BENZYL ALCOHOL-INDUCED LIPID INTERDIGITATED PHASE, Archives of biochemistry and biophysics, 333(2), 1996, pp. 401-406
To further investigate factors contributing to the action of alcohol i
n the solute-induced lipid interdigitation phase, thermodynamic and fl
uorescence polarization measurements were carried out to study the int
eraction of benzyl alcohol with dipalmitoyl phosphatidylcholine bilaye
r vesicles. The obtained results were compared with those previously r
eported for ethanol and cyclohexanol (L. G. Roth and C-H, Chen, Arch.
Biochem. Biophys. 296, 207, 1992). Similar to ethanol, benzyl alcohol
was found to exhibit a biphasic effect on the enthalpy (Delta H-m) and
the temperature (t(m)) of the lipid-phase transition and the steady-s
tate fluorescence polarization (P) monitored by 1,6-diphenyl-1,3,5-hex
atriene, At a total concentration of benzyl alcohol <30 mg/ml (the alc
ohol concentration in lipid phase <21 mg/ml), benzyl alcohol was found
to exhibit large increases in Delta H-m and P, which were correlated
with the formation of a lipid interdigitated phase, as evidenced by re
ported X-ray diffraction data. Combining the results with benzyl alcoh
ol and ethanol suggested that simultaneously large changes in Delta H-
m and P can be used as an indication of the occurrence of a solute-ind
uced lipid interdigitated phase. The overall interacting force in the
formation of this lipid phase, as derived from the interactions of the
hydroxyl portion of an alcohol with the lipid phosphate head group an
d the hydrophobic portion of an alcohol with the lipid hydrocarbon cha
ins, may or may not be dominated by hydrophobic interaction, Although
lipid/water partition coefficients and the contribution of hydrophobic
interaction to the overall interacting force were comparable between
benzyl alcohol and cyclohexanol, benzyl alcohol induced lipid interdig
itated phase, but not for cyclohexanol, This was due to the ability of
benzyl alcohol to be more effective than cyclohexanol in simultaneous
ly interacting with the phosphate head group and the hydrocarbon chain
s of lipid. (C) 1996 Academic Press, Inc.