%0 Journal Article
%T Gelatin degradation assay reveals MMP-9 inhibitors and function of O-glycosylated domain
%A Jennifer Vandooren
%A Nathalie Geurts
%A Erik Martens
%A Philippe E Van den Steen
%J World Journal of Biological Chemistry
%D 2011
%I Baishideng Publishing Group Co. Limited
%X AIM: To establish a novel, sensitive and high-throughput gelatinolytic assay to define new inhibitors and compare domain deletion mutants of gelatinase B/matrix metalloproteinase (MMP)-9.METHODS: Fluorogenic Dye-quenched (DQ) -gelatin was used as a substrate and biochemical parameters (substrate and enzyme concentrations, DMSO solvent concentrations) were optimized to establish a high-throughput assay system. Various small-sized libraries (ChemDiv, InterBioScreen and ChemBridge) of heterocyclic, drug-like substances were tested and compared with prototypic inhibitors.RESULTS: First, we designed a test system with gelatin as a natural substrate. Second, the assay was validated by selecting a novel pyrimidine-2,4,6-trione (barbiturate) inhibitor. Third, and in line with present structural data on collagenolysis, it was found that deletion of the O-glycosylated region significantly decreased gelatinolytic activity (kcat/kM ¡À 40% less than full-length MMP-9).CONCLUSION: The DQ -gelatin assay is useful in high-throughput drug screening and exosite targeting. We demonstrate that flexibility between the catalytic and hemopexin domain is functionally critical for gelatinolysis.
%K Exosite inhibitors
%K Fluorogenic substrate
%K Gelatin
%K High-throughput screening assays
%K Matrix metalloproteinase-9
%K Substrate specificity
%U http://www.wjgnet.com/1949-8454/full/v2/i1/14.htm