Synthesis of N epsilon-(7-diethylaminocoumarin-3-carboxyl)- and N epsilon-(7-methoxycoumarin-3-carboxyl)-L-Fmoc lysine as tools for protease cleavage detection by fluorescence

Autor:	Thomas, Berthelot, Jean-Claude, Talbot, Georges, Laïn, Gérard, Déleris, Laurent, Latxague
Rok vydání:	2005
Předmět:	Kinetics Molecular Structure Coumarins Lysine Fluorescence Resonance Energy Transfer Matrix Metalloproteinase 1 Chromatography High Pressure Liquid Fluorescence
Zdroj:	Journal of peptide science : an official publication of the European Peptide Society. 11(3)
ISSN:	1075-2617
Popis:	Two coumarin-labelled lysines were conveniently prepared as a fluorescence resonance energy transfer (FRET) pair for peptide cleavage detection. 7-Methoxy and 7-diethylamino coumarin-3-carboxylic acids were synthesized according to a modification of known procedures. Labelling at lysine was achieved in solution via the active N-hydroxysuccinimide ester of the carboxylic acid coumarin derivatives to give the target compounds in good yield. Subsequently, these modified amino acids were used in solid phase peptide synthesis (SPPS), and their potential utility in an extracellular matrix metalloprotease (MMP-1) activity measurement via FRET and/or quenching studies was demonstrated.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::203d05246b92304d56baa08de50185ec https://pubmed.ncbi.nlm.nih.gov/15635646 Zobrazit plný text záznamu Plný text