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Biophys J, April 2002, p. 1743-1755, Vol. 82, No. 4
and
*Department of Mathematics and Statistics, University of New
Mexico, Albuquerque, New Mexico 87131, and
Theoretical
Biology and Biophysics Group, Theoretical Division, Los Alamos National
Laboratory, Los Alamos, New Mexico 87545 USA
In the Biacore biosensor, a widely used tool for studying
the kinetics of ligand/receptor binding, receptors are commonly localized to the sensor surface through attachment to polymers that
extend from the surface to form a layer. The importance of the
polymeric layer in analyzing data is controversial. The question of the
effect of a binding layer also arises in the case of ligands interacting with binding sites distributed in the extracellular matrix
of cells. To identify and quantify the effects of a binding layer on
the estimation of association and dissociation rate constants, we
derived effective rate coefficients. The expressions show that rate
constants determined under the standard assumption that binding takes
place on a two-dimensional surface underestimate the true reaction rate
constants by a factor that depends on the ratio of the height of the
layer to the mean free path of the ligand within the layer. We show
that, for typical biological ligands, receptors, cells, and Biacore
conditions, the binding layer will affect the interpretation of data
only if transport of the ligand in the layer is slowed
substantially
by one or two orders of magnitude
relative to transport
outside the layer. From existing experiments and theory, it is not
clear which Biacore experiments, if any, have transport within the
dextran layer reduced to such an extent. We propose a method, based on
the effective rate coefficients we have derived, for the experimental
determination of ligand diffusion coefficients in a polymeric matrix.
Biophys J, April 2002, p. 1743-1755, Vol. 82, No. 4
© 2002 by the Biophysical Society 0006-3495/02/04/1743/13 $2.00
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