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Biophys J, July 1998, p. 159-173, Vol. 75, No. 1
and
*Department of Physical Chemistry and the Fritz Haber Research
Center, The Hebrew University of Jerusalem, Jerusalem 91904, Israel,
and
Department of Chemistry and Biochemistry, University
of California Los Angeles, Los Angeles, California 90095 USA
We develop a statistical thermodynamic model for the
phase evolution of DNA-cationic lipid complexes in aqueous solution, as
a function of the ratios of charged to neutral lipid and charged lipid
to DNA. The complexes consist of parallel strands of DNA intercalated
in the water layers of lamellar stacks of mixed lipid bilayers, as
determined by recent synchrotron x-ray measurements. Elastic
deformations of the DNA and the lipid bilayers are neglected, but
DNA-induced spatial inhomogeneities in the bilayer charge densities are
included. The relevant nonlinear Poisson-Boltzmann equation is solved
numerically, including self-consistent treatment of the boundary
conditions at the polarized membrane surfaces. For a wide range of
lipid compositions, the phase evolution is characterized by three
regions of lipid to DNA charge ratio,
: 1) for low
, the
complexes coexist with excess DNA, and the DNA-DNA spacing in the
complex, d, is constant; 2) for intermediate
, including
the isoelectric point
= 1, all of the lipid and DNA in solution is
incorporated into the complex, whose inter-DNA distance d
increases linearly with
; and 3) for high
, the complexes coexist
with excess liposomes (whose lipid composition is different from that
in the complex), and their spacing d is nearly, but not
completely, independent of
. These results can be understood in
terms of a simple charging model that reflects the competition between
counterion entropy and inter-DNA (
< 1) and interbilayer (
> 1)
repulsions. Finally, our approach and conclusions are compared with
theoretical work by others, and with relevant experiments.
Biophys J, July 1998, p. 159-173, Vol. 75, No. 1
© 1998 by the Biophysical Society 0006-3495/98/07/159/15 $2.00
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