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A Molecular Probe with Both Chromogenic and Fluorescent Units for Detecting Serine Proteases

A molecular probe with l-phenylalanine p-nitroanilide and l-lysin 4-methylcoumaryl-7-amide, in which these amino acid derivatives are connected through a succinic-acid spacer, was prepared. Trypsin and papain were detected by blue-fluorescence emission of generated 7-amino-4-methylcoumarin (AMC). α-...

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Detalles Bibliográficos
Autores principales: Ishida, Kirara, Nakamura, Yushi, Ohta, Tetsuo, Oe, Yohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831087/
https://www.ncbi.nlm.nih.gov/pubmed/33477543
http://dx.doi.org/10.3390/molecules26020482
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author Ishida, Kirara
Nakamura, Yushi
Ohta, Tetsuo
Oe, Yohei
author_facet Ishida, Kirara
Nakamura, Yushi
Ohta, Tetsuo
Oe, Yohei
author_sort Ishida, Kirara
collection PubMed
description A molecular probe with l-phenylalanine p-nitroanilide and l-lysin 4-methylcoumaryl-7-amide, in which these amino acid derivatives are connected through a succinic-acid spacer, was prepared. Trypsin and papain were detected by blue-fluorescence emission of generated 7-amino-4-methylcoumarin (AMC). α-Chymotrypsin and nattokinase were detected from both the blue-fluorescence emission of AMC and the UV absorbance of p-nitroaniline. In addition, different time courses of p-nitroaniline and AMC were observed between the reaction of P1 with α-chymotrypsin and that with nattokinase. In the case of nattokinase, both the fluorescence emission and UV absorbance slowly increased. In contrast, the increasing UV absorbance was saturated at the early stage of the reaction of the present probe with chymotrypsin, whereas the fluorescence emission continuously increased in the following stages.
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spelling pubmed-78310872021-01-26 A Molecular Probe with Both Chromogenic and Fluorescent Units for Detecting Serine Proteases Ishida, Kirara Nakamura, Yushi Ohta, Tetsuo Oe, Yohei Molecules Article A molecular probe with l-phenylalanine p-nitroanilide and l-lysin 4-methylcoumaryl-7-amide, in which these amino acid derivatives are connected through a succinic-acid spacer, was prepared. Trypsin and papain were detected by blue-fluorescence emission of generated 7-amino-4-methylcoumarin (AMC). α-Chymotrypsin and nattokinase were detected from both the blue-fluorescence emission of AMC and the UV absorbance of p-nitroaniline. In addition, different time courses of p-nitroaniline and AMC were observed between the reaction of P1 with α-chymotrypsin and that with nattokinase. In the case of nattokinase, both the fluorescence emission and UV absorbance slowly increased. In contrast, the increasing UV absorbance was saturated at the early stage of the reaction of the present probe with chymotrypsin, whereas the fluorescence emission continuously increased in the following stages. MDPI 2021-01-18 /pmc/articles/PMC7831087/ /pubmed/33477543 http://dx.doi.org/10.3390/molecules26020482 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ishida, Kirara
Nakamura, Yushi
Ohta, Tetsuo
Oe, Yohei
A Molecular Probe with Both Chromogenic and Fluorescent Units for Detecting Serine Proteases
title A Molecular Probe with Both Chromogenic and Fluorescent Units for Detecting Serine Proteases
title_full A Molecular Probe with Both Chromogenic and Fluorescent Units for Detecting Serine Proteases
title_fullStr A Molecular Probe with Both Chromogenic and Fluorescent Units for Detecting Serine Proteases
title_full_unstemmed A Molecular Probe with Both Chromogenic and Fluorescent Units for Detecting Serine Proteases
title_short A Molecular Probe with Both Chromogenic and Fluorescent Units for Detecting Serine Proteases
title_sort molecular probe with both chromogenic and fluorescent units for detecting serine proteases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831087/
https://www.ncbi.nlm.nih.gov/pubmed/33477543
http://dx.doi.org/10.3390/molecules26020482
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