The goal of this paper is to measure the overall reaction rate of irre
versibly adsorbed but mobile enzymes on substrate-coated surfaces and
to model the interplay between reaction and diffusion in this system.
Our model system uses collagenase, an enzyme that degrades native coll
agen, and synthetic surfaces covered with a peptide that is a substrat
e for collagenase. We employ a multisurface flow cell device to measur
e the change of ultraviolet absorbance as collagenase hydrolyzes the s
urface-bound peptide substrate. The overall reaction rate is enhanced
as the surface enzyme concentration is increased. By changing the buff
er pH we discern the influence of the intrinsic kinetic rate on the ov
erall reaction rate. Employing surfaces containing fewer bound substra
tes, we probe the effect of the distance between substrates on the ove
rall reaction rate to show that this process is governed by both react
ion and diffusion. Using a modified Smoluchowski theory, we model this
interplay to determine the intrinsic reaction rate of the surface pro
cess and compare this value to those found for collagenase reaction in
solution. (C) 1995 Academic Press, Inc.