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Biophys J, September 2000, p. 1237-1252, Vol. 79, No. 3


and
*Max-Planck-Institut für Strahlenchemie, Ruhr 45470, Germany;
Department of Chemistry, University of California at
Riverside, Riverside, California 92521 USA; and
Institute for Physics, National Academy of
Science-Ukraine, Kyiv 252028, Ukraine
A model for light-induced charge separation in a
donor-acceptor system of the reaction center of photosynthetic bacteria
is described. This description is predicated on a self-regulation of
the flow of photo-activated electrons due to self-consistent, slow
structural rearrangements of the macromolecule. Effects of the
interaction between the separated charges and the slow structural modes
of the biomolecule may accumulate during multiple, sequential charge
transfer events. This accumulation produces non-linear dynamic effects
on system function, providing a regulation of the charge separation
efficiency. For a biomolecule with a finite number of different
charge-transfer states, the quasi-stationary populations of these
states with a localized electron on different cofactors may deviate
from a Lagmuir law dependence with actinic light intensity. Such
deviations are predicted by the model to be due to light-induced
structural changes. The theory of self-regulation developed here
assumes that light-induced changes in the effective adiabatic potential
occur along a slow structural coordinate. In this model, a
"light-adapted" conformational state appears when bifurcation
produces a new minimum in the adiabatic potential. In this state, the
lifetime of the charge-separated state may be quite different from that
of the "dark-adapted" conformation. The results predicted by this
theory agree with previously obtained experimental results on
photosynthetic reaction centers.
Biophys J, September 2000, p. 1237-1252, Vol. 79, No. 3
© 2000 by the Biophysical Society 0006-3495/00/09/1237/16 $2.00
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