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Biophys J, January 2002, p. 76-92, Vol. 82, No. 1
and
*Fakultät für Physik, Universität Konstanz, 78457 Konstanz, and
Max-Planck-Institut für Kolloid- und
Grenzflächenforschung, 14424 Potsdam, Germany
We consider a planar stiff model membrane consisting of
mobile surface groups whose state of charge depends on the pH and the
ionic composition of the adjacent electrolyte solution. To calculate
the mean-field interaction potential between a charged object and such
a model membrane, one needs to solve a Poisson-Boltzmann boundary
value problem. We here derive and discuss the boundary condition at the
membrane surface, a condition that is generally appropriate for
biological membranes where two charge-regulating mechanisms are present
at the same time: the pH-dependent chemical charge regulation and a
regulation through the in-plane mobility of the surface groups. As an
application of this general formalism, we consider the specific example
of a single DNA molecule, approximated by a cylinder with smeared-out
surface charges, interacting with such a model membrane. We study the
effect that the two competing charge-regulating mechanisms have on the
DNA/membrane interaction and the distribution of surface ions in the
plane of the membrane. We find that, at short DNA-membrane distances,
membrane fluidity can have a considerable impact on the DNA adsorption
behavior and can lead to such counterintuitive phenomena as the
adsorption of a negatively charged DNA onto a (on average) negatively
charged membrane.
Biophys J, January 2002, p. 76-92, Vol. 82, No. 1
© 2002 by the Biophysical Society 0006-3495/02/01/76/17 $2.00
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