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Triple-FRET multi-purpose fluorescent probe for three-protease detection

A new, robust and reliable methodology for three-protease screening in a single-enzyme mode has been developed and verified, employing a multi-purpose peptide probe with three selectively cleavable sites furnished with four fluorophores. A triple-FRET-based single-excitation quadruple-emission conce...

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Detalles Bibliográficos
Autores principales: Milićević, David, Hlaváč, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549473/
https://www.ncbi.nlm.nih.gov/pubmed/36320525
http://dx.doi.org/10.1039/d2ra05125g
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author Milićević, David
Hlaváč, Jan
author_facet Milićević, David
Hlaváč, Jan
author_sort Milićević, David
collection PubMed
description A new, robust and reliable methodology for three-protease screening in a single-enzyme mode has been developed and verified, employing a multi-purpose peptide probe with three selectively cleavable sites furnished with four fluorophores. A triple-FRET-based single-excitation quadruple-emission concept for unambiguous sensing of trypsin, chymotrypsin and caspase-8 in the lowest detectable concentrations of 0.5 ng mL(−1), 0.2 μg mL(−1), and 2 U mL(−1), respectively, has been applied and graphically depicted. Then the developed 4-dye probe has been also studied from the perspective of simultaneous two-protease screening, which was found only partially feasible, primarily due to unselective chymotrypsin cleavage.
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spelling pubmed-95494732022-10-31 Triple-FRET multi-purpose fluorescent probe for three-protease detection Milićević, David Hlaváč, Jan RSC Adv Chemistry A new, robust and reliable methodology for three-protease screening in a single-enzyme mode has been developed and verified, employing a multi-purpose peptide probe with three selectively cleavable sites furnished with four fluorophores. A triple-FRET-based single-excitation quadruple-emission concept for unambiguous sensing of trypsin, chymotrypsin and caspase-8 in the lowest detectable concentrations of 0.5 ng mL(−1), 0.2 μg mL(−1), and 2 U mL(−1), respectively, has been applied and graphically depicted. Then the developed 4-dye probe has been also studied from the perspective of simultaneous two-protease screening, which was found only partially feasible, primarily due to unselective chymotrypsin cleavage. The Royal Society of Chemistry 2022-10-10 /pmc/articles/PMC9549473/ /pubmed/36320525 http://dx.doi.org/10.1039/d2ra05125g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Milićević, David
Hlaváč, Jan
Triple-FRET multi-purpose fluorescent probe for three-protease detection
title Triple-FRET multi-purpose fluorescent probe for three-protease detection
title_full Triple-FRET multi-purpose fluorescent probe for three-protease detection
title_fullStr Triple-FRET multi-purpose fluorescent probe for three-protease detection
title_full_unstemmed Triple-FRET multi-purpose fluorescent probe for three-protease detection
title_short Triple-FRET multi-purpose fluorescent probe for three-protease detection
title_sort triple-fret multi-purpose fluorescent probe for three-protease detection
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549473/
https://www.ncbi.nlm.nih.gov/pubmed/36320525
http://dx.doi.org/10.1039/d2ra05125g
work_keys_str_mv AT milicevicdavid triplefretmultipurposefluorescentprobeforthreeproteasedetection
AT hlavacjan triplefretmultipurposefluorescentprobeforthreeproteasedetection