The effect of channel-forming peptide gramicidin A on the dipole potential
of phospholipid monolayers and bilayers has been studied. Surface pressure
and surface potential isotherms of monolayers have been measured with a Lan
gmuir trough equipped with a Wilhelmy balance and a surface potential meter
(Kelvin probe). Gramicidin has been shown to shift pressure-area isotherms
of phospholipids and to reduce their monolayer surface potentials. Both ef
fects increase with the increase in gramicidin concentration and depend on
the kind of phosphatidylcholine used. Application of the dual-wavelength ra
tiometric fluorescence method using the potential-sensitive dye RH421 has r
evealed that the addition of gramicidin A to dipalmitoylphosphatidylcholine
liposomes leads to a decrease in the fluorescence ratio of RH421. This is
similar to the effect of phloretin, which is known to decrease the dipole p
otential. The comparison of the concentration dependences of the fluorescen
ce ratio for gramicidin and phloretin shows that gramicidin is as potent as
phloretin in modifying the membrane dipole potential.