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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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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. |
format | Online Article Text |
id | pubmed-5615226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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
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title_full | Kinase-templated abiotic reaction
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title_fullStr | Kinase-templated abiotic reaction
|
title_full_unstemmed | Kinase-templated abiotic reaction
|
title_short | Kinase-templated abiotic reaction
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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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