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Biophys J, February 2002, p. 865-873, Vol. 82, No. 2
A. N. Belozersky Institute of Physico-Chemical Biology, Moscow State University, Moscow 119899 Russia
The effect of membrane dipole potential on gramicidin
channel activity in bilayer lipid membranes (BLMs) was studied.
Remarkably, it appeared that proton conductance of gramicidin A (gA)
channels responded to modulation of the dipole potential oppositely as compared with gA alkali metal cation conductance. In particular, the
addition of phloretin, known to reduce the membrane dipole potential,
resulted in a decrease in gA proton conductance, on one hand, and an
increase in gA alkali metal conductance, on the other hand, whereas
6-ketocholestanol, the agent raising the membrane dipole potential,
provoked an increase in gA proton conductance as opposed to a decrease
in the alkali metal cation conductance. The peculiarity of the
6-ketocholestanol effect consisted in its dependence on the
H+ concentration. The experiments with the impermeant
dipolar compound, phloridzin, showed that the response of proton
transport through gramicidin channels to varying the membrane dipole
potential did not change qualitatively if the dipole potential of only
one monolayer or both monolayers of the BLM was altered. In contrast to
gA proton conductance, the single-channel lifetime changed similarly
with varying the membrane dipole potential, regardless of the kind of
permeant cations (protons or potassium ions). The results of this study
could be tentatively accounted for by an assumption that one of the
rate-limiting steps of proton conduction through gramicidin channels
represents, in fact, movement of negatively charged species (negative
ionic defects) across a membrane.
Biophys J, February 2002, p. 865-873, Vol. 82, No. 2
© 2002 by the Biophysical Society 0006-3495/02/02/865/09 $2.00
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