ENZYMES ON IMMOBILIZED SUBSTRATE SURFACES - REACTION

Citation
Pb. Gaspers et al., ENZYMES ON IMMOBILIZED SUBSTRATE SURFACES - REACTION, Journal of colloid and interface science, 172(2), 1995, pp. 518-529
Citations number
41
Categorie Soggetti
Chemistry Physical
ISSN journal
00219797
Volume
172
Issue
2
Year of publication
1995
Pages
518 - 529
Database
ISI
SICI code
0021-9797(1995)172:2<518:EOISS->2.0.ZU;2-Y
Abstract
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.