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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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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. |
format | Online Article Text |
id | pubmed-9549473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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 |