2011
DOI: 10.5483/bmbrep.2011.44.7.458
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A fluorogenic method for measuring enteropeptidase activity: spectral shift in the emission of GD4K-conjugated 7-amino-4-methylcoumarin

Abstract: Fig. 1. Structure of 2-naphthylamine (A) and 7-amino-4-methylcoumarin (B).A fluorogenic method for measuring enteropeptidase activity: spectral shift in the emission of GD 4 K-conjugated 7-amino-4-methylcoumarin Enteropeptidase is a serine protease secreted by the pancreas and converts inactive trypsinogen to active trypsin. Enteropeptidase cleaves the C-terminal end of the substrate recognition sequence Asp-Asp-Asp-Asp-Lys (D4K). The assay for enteropeptidase has utilized GD4K-conjugated 2-naphthylamine (GD4K… Show more

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Cited by 3 publications
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“…All enteropeptidase enzyme assay and compound evaluation were conducted at pH 8 because the optimal pH of enteropeptidase was 8 as previously reported; Magee et al …”
Section: Methodsmentioning
confidence: 99%
“…All enteropeptidase enzyme assay and compound evaluation were conducted at pH 8 because the optimal pH of enteropeptidase was 8 as previously reported; Magee et al …”
Section: Methodsmentioning
confidence: 99%
“…C120 is also a well-known laboratory reagent, employed as a uorogenic probe for detection of enzymatic activity. 51 This dye has been used as a uorescence probe to analyze glycoproteins, monosaccharides and N-linked oligosaccharides via chromatography. 52 C120 has also shown effective antitubercular, 53 antibacterial and antifungal 54 activities.…”
Section: Introductionmentioning
confidence: 99%