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Fluorogenic substrates for chymotrypsin with 2-quinolinone derivatives as leaving groups.

作者信息

Kokotos G, Geiger R, Tzougraki C

机构信息

Department of Chemistry, University of Athens.

出版信息

Biol Chem Hoppe Seyler. 1990 Sep;371(9):835-40. doi: 10.1515/bchm3.1990.371.2.835.

DOI:10.1515/bchm3.1990.371.2.835
PMID:1963307
Abstract

Sensitive and convenient fluorometric assays for the determination of chymotrypsin have been developed by using the substrates Glt-Leu-Phe-NH-Meq, Glt-Phe-NH-FMeq and Glt-Leu-Phe-NH-FMeq, which have been synthesized utilizing the mixed anhydride method. The amidolytic activity of chymotrypsin was measured by the release of the highly fluorescent amine 7-amino-4-methyl-2-quinolinone (AMeq) or 7-amino-4-trifluoromethyl-2-quinolinone (AFMeq). The fluorescence properties of the synthesized substrates and the new fluorescent marker AFMeq were examined. Kinetic constants, as well as the maximum sensitivity for the hydrolysis of the new substrates, were determined. All new substrates permit a rapid and sensitive determination of chymotrypsin in a continuous assay system. As little as 0.7 ng of enzyme can be detected using the substrate Glt-Leu-Phe-NH-Meq, which is the most sensitive fluorogenic substrate thus far reported.

摘要

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