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Label‐Free Fluorescent Kinase and Phosphatase Enzyme Assays with Supramolecular Host‐Dye Pairs

The combination of the macrocyclic hosts p‐sulfonatocalix[4]arene and cucurbit[7]uril with the fluorescent dyes lucigenin and berberine affords two label‐free enzyme assays for the detection of kinase and phosphatase activity by fluorescence monitoring. In contrast to established assays, no substrat...

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Autores principales: Liu, Yan‐Cen, Peng, Shu, Angelova, Lora, Nau, Werner M., Hennig, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848908/
https://www.ncbi.nlm.nih.gov/pubmed/31741820
http://dx.doi.org/10.1002/open.201900299
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author Liu, Yan‐Cen
Peng, Shu
Angelova, Lora
Nau, Werner M.
Hennig, Andreas
author_facet Liu, Yan‐Cen
Peng, Shu
Angelova, Lora
Nau, Werner M.
Hennig, Andreas
author_sort Liu, Yan‐Cen
collection PubMed
description The combination of the macrocyclic hosts p‐sulfonatocalix[4]arene and cucurbit[7]uril with the fluorescent dyes lucigenin and berberine affords two label‐free enzyme assays for the detection of kinase and phosphatase activity by fluorescence monitoring. In contrast to established assays, no substrate labeling is required. Since phosphorylation is one of the most important regulatory mechanisms in biological signal transduction, the assays should be useful for identification of inhibitors and activators in high‐throughput screening (HTS) format for drug discovery.
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spelling pubmed-68489082019-11-18 Label‐Free Fluorescent Kinase and Phosphatase Enzyme Assays with Supramolecular Host‐Dye Pairs Liu, Yan‐Cen Peng, Shu Angelova, Lora Nau, Werner M. Hennig, Andreas ChemistryOpen Communications The combination of the macrocyclic hosts p‐sulfonatocalix[4]arene and cucurbit[7]uril with the fluorescent dyes lucigenin and berberine affords two label‐free enzyme assays for the detection of kinase and phosphatase activity by fluorescence monitoring. In contrast to established assays, no substrate labeling is required. Since phosphorylation is one of the most important regulatory mechanisms in biological signal transduction, the assays should be useful for identification of inhibitors and activators in high‐throughput screening (HTS) format for drug discovery. John Wiley and Sons Inc. 2019-11-12 /pmc/articles/PMC6848908/ /pubmed/31741820 http://dx.doi.org/10.1002/open.201900299 Text en ©2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Liu, Yan‐Cen
Peng, Shu
Angelova, Lora
Nau, Werner M.
Hennig, Andreas
Label‐Free Fluorescent Kinase and Phosphatase Enzyme Assays with Supramolecular Host‐Dye Pairs
title Label‐Free Fluorescent Kinase and Phosphatase Enzyme Assays with Supramolecular Host‐Dye Pairs
title_full Label‐Free Fluorescent Kinase and Phosphatase Enzyme Assays with Supramolecular Host‐Dye Pairs
title_fullStr Label‐Free Fluorescent Kinase and Phosphatase Enzyme Assays with Supramolecular Host‐Dye Pairs
title_full_unstemmed Label‐Free Fluorescent Kinase and Phosphatase Enzyme Assays with Supramolecular Host‐Dye Pairs
title_short Label‐Free Fluorescent Kinase and Phosphatase Enzyme Assays with Supramolecular Host‐Dye Pairs
title_sort label‐free fluorescent kinase and phosphatase enzyme assays with supramolecular host‐dye pairs
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848908/
https://www.ncbi.nlm.nih.gov/pubmed/31741820
http://dx.doi.org/10.1002/open.201900299
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