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Kinase-templated abiotic reaction

Protein kinases are quintessential regulators of cellular function. Numerous pathologies are intimately linked to the dysregulated activity of a particular protein kinase. Herein we report a technology based on a proximity-induced chemical transformation that enables the detection and imaging of spe...

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Autores principales: Saarbach, J., Lindberg, E., Folliet, S., Georgeon, S., Hantschel, O., Winssinger, N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615226/
https://www.ncbi.nlm.nih.gov/pubmed/28970898
http://dx.doi.org/10.1039/c7sc01416c
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author Saarbach, J.
Lindberg, E.
Folliet, S.
Georgeon, S.
Hantschel, O.
Winssinger, N.
author_facet Saarbach, J.
Lindberg, E.
Folliet, S.
Georgeon, S.
Hantschel, O.
Winssinger, N.
author_sort Saarbach, J.
collection PubMed
description Protein kinases are quintessential regulators of cellular function. Numerous pathologies are intimately linked to the dysregulated activity of a particular protein kinase. Herein we report a technology based on a proximity-induced chemical transformation that enables the detection and imaging of specific kinases. Using two probes that target the nucleotide-binding site and substrate binding site of a target kinase respectively, the reagents appended on the probes are brought within reactive distance thereby enabling the chemical transformation. The reaction used for sensing is a ruthenium-photocatalyzed reduction of a pyridinium immolative linker, which uncages a fluorophore (rhodamine). We demonstrate that this technology can be used to discriminate between closely related kinases with a high signal to noise ratio. We further demonstrate that the technology operates within the complexity of a cellular context with a good correlation between the level of kinase activity and fluorescence output.
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spelling pubmed-56152262017-10-02 Kinase-templated abiotic reaction Saarbach, J. Lindberg, E. Folliet, S. Georgeon, S. Hantschel, O. Winssinger, N. Chem Sci Chemistry Protein kinases are quintessential regulators of cellular function. Numerous pathologies are intimately linked to the dysregulated activity of a particular protein kinase. Herein we report a technology based on a proximity-induced chemical transformation that enables the detection and imaging of specific kinases. Using two probes that target the nucleotide-binding site and substrate binding site of a target kinase respectively, the reagents appended on the probes are brought within reactive distance thereby enabling the chemical transformation. The reaction used for sensing is a ruthenium-photocatalyzed reduction of a pyridinium immolative linker, which uncages a fluorophore (rhodamine). We demonstrate that this technology can be used to discriminate between closely related kinases with a high signal to noise ratio. We further demonstrate that the technology operates within the complexity of a cellular context with a good correlation between the level of kinase activity and fluorescence output. Royal Society of Chemistry 2017-07-01 2017-05-24 /pmc/articles/PMC5615226/ /pubmed/28970898 http://dx.doi.org/10.1039/c7sc01416c Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Saarbach, J.
Lindberg, E.
Folliet, S.
Georgeon, S.
Hantschel, O.
Winssinger, N.
Kinase-templated abiotic reaction
title Kinase-templated abiotic reaction
title_full Kinase-templated abiotic reaction
title_fullStr Kinase-templated abiotic reaction
title_full_unstemmed Kinase-templated abiotic reaction
title_short Kinase-templated abiotic reaction
title_sort kinase-templated abiotic reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615226/
https://www.ncbi.nlm.nih.gov/pubmed/28970898
http://dx.doi.org/10.1039/c7sc01416c
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