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PMID: 2479283 Published · ppublish English Journal Article

A semicontinuous, high-performance liquid chromatography-based assay for stromelysin.

Analytical biochemistry ·Vol. 180 ·No. 1 ·1989-07-00 ·Pages 110-3

Harrison R, Teahan J, Stein R

Abstract

A search for low molecular weight peptide substrates for the metalloendoproteinase, human fibroblast stromelysin, resulted in the discovery that substance P (Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2) is a substrate for this enzyme and is cleaved exclusively at the Gln6-Phe7 bond. On the basis of this observation, a semicontinuous HPLC-based assay was developed that monitors the production of the hydrolysis product, fragment 7-11 (SP7-11). Steady-state velocities for the production of SP7-11 have been determined as a function of substrate concentration and obey simple, Michaelis-Menten kinetics. For a 1-ml reaction volume, Vmax = (2.4 nmol SP7-11/min)/micrograms protein and Km = 0.38 mM.

MeSH Terms
Chromatography, High Pressure Liquid/methods Enzyme Activation/drug effects Hydrolysis Kinetics Matrix Metalloproteinase 3 Metalloendopeptidases/analysis,metabolism Peptide Fragments/metabolism Phenylmercuric Acetate/analogs & derivatives,pharmacology Substance P/metabolism Substrate Specificity
Chemicals
Peptide Fragments Substance P substance P (7-11) 4-aminophenylmercuriacetate Metalloendopeptidases Matrix Metalloproteinase 3 Phenylmercuric Acetate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Harrison R
Department of Enzymology, Merck Sharp and Dohme Research Laboratories, Rahway, New Jersey 07065.
Teahan J
Stein R
Article Info
Journal
Analytical biochemistry
Abbr.
Anal Biochem
ISSN
0003-2697
Published
1989-07-00
Pages
110-3
Language
English
Region
United States
NLM ID
0370535
Subset
IM
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