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Biophys J, February 2001, p. 668-682, Vol. 80, No. 2
and
*Department of Chemical Engineering and Institute of Medicine and
Engineering, University of Pennsylvania, Philadelphia, Pennsylvania
19104; and
Department of Pharmacology and Physiology,
University of Rochester, Rochester, New York 14642 USA
A microcantilever technique was used to apply force to
receptor-ligand molecules involved in leukocyte rolling on blood vessel walls. E-selectin was adsorbed onto 3-µm-diameter, 4-mm-long glass fibers, and the selectin ligand, sialyl Lewisx, was coupled
to latex microspheres. After binding, the microsphere and bound fiber
were retracted using a computerized loading protocol that combines
hydrodynamic and Hookean forces on the fiber to produce a range of
force loading rates (force/time), rf. From the
distribution of forces at failure, the average force was determined and
plotted as a function of ln rf. The slope and
intercept of the plot yield the unstressed reverse reaction rate,
kro, and a parameter that describes the
force dependence of reverse reaction rates, ro.
The ligand was titrated so adhesion occurred in ~30% of tests,
implying that >80% of adhesive events involve single bonds. Monte
Carlo simulations show that this level of multiple bonding has little
effect on parameter estimation. The estimates are
ro = 0.048 and 0.016 nm and
kro = 0.72 and 2.2 s
1 for
loading rates in the ranges 200-1000 and 1000-5000 pN
s
1, respectively. Levenberg-Marquardt fitting across all
values of rf gives
ro = 0.034 nm and
kro = 0.82 s
1. The values of
these parameters are in the range required for rolling, as suggested by
adhesive dynamics simulations.
Biophys J, February 2001, p. 668-682, Vol. 80, No. 2
© 2001 by the Biophysical Society 0006-3495/01/02/668/15 $2.00
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