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Cationic Europium Complexes for Visualizing Fluctuations in Mitochondrial ATP Levels in Living Cells
The ability to study cellular metabolism and enzymatic processes involving adenosine triphosphate (ATP) is impeded by the lack of imaging probes capable of signalling the concentration and distribution of intracellular ATP rapidly, with high sensitivity. We report here the first example of a lumines...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175470/ https://www.ncbi.nlm.nih.gov/pubmed/29761917 http://dx.doi.org/10.1002/chem.201801008 |
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author | Mailhot, Romain Traviss‐Pollard, Thomas Pal, Robert Butler, Stephen J. |
author_facet | Mailhot, Romain Traviss‐Pollard, Thomas Pal, Robert Butler, Stephen J. |
author_sort | Mailhot, Romain |
collection | PubMed |
description | The ability to study cellular metabolism and enzymatic processes involving adenosine triphosphate (ATP) is impeded by the lack of imaging probes capable of signalling the concentration and distribution of intracellular ATP rapidly, with high sensitivity. We report here the first example of a luminescent lanthanide complex capable of visualizing changes in the concentration of ATP in the mitochondria of living cells. Four cationic europium(III) complexes [Eu.1–4](+) have been synthesized and their binding capabilities towards nucleoside polyphosphate anions examined in aqueous solution at physiological pH. Complexes [Eu.1](+) and [Eu.3](+) bearing hydrogen bond donor groups in the pendant arms showed excellent discrimination between ATP, ADP and monophosphate species. Complex [Eu.3](+) showed relatively strong binding to ATP (logK (a)=5.8), providing a rapid, long‐lived luminescent signal that enabled its detection in a highly competitive aqueous medium containing biologically relevant concentrations of Mg(2+), ADP, GTP, UTP and human serum albumin. This Eu(III) complex responds linearly to ATP within the physiological concentration range (1–5 mm), and was used to continuously monitor the apyrase‐catalyzed hydrolysis of ATP to ADP in vitro. We demonstrate that [Eu.3](+) can permeate mammalian (NIH‐3T3) cells efficiently and localize to the mitochondria selectively, permitting real‐time visualization of elevated mitochondrial ATP levels following treatment with a broad spectrum kinase inhibitor, staurosporine, as well as depleted ATP levels upon treatment with potassium cyanide under glucose starvation conditions. |
format | Online Article Text |
id | pubmed-6175470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61754702018-10-19 Cationic Europium Complexes for Visualizing Fluctuations in Mitochondrial ATP Levels in Living Cells Mailhot, Romain Traviss‐Pollard, Thomas Pal, Robert Butler, Stephen J. Chemistry Full Papers The ability to study cellular metabolism and enzymatic processes involving adenosine triphosphate (ATP) is impeded by the lack of imaging probes capable of signalling the concentration and distribution of intracellular ATP rapidly, with high sensitivity. We report here the first example of a luminescent lanthanide complex capable of visualizing changes in the concentration of ATP in the mitochondria of living cells. Four cationic europium(III) complexes [Eu.1–4](+) have been synthesized and their binding capabilities towards nucleoside polyphosphate anions examined in aqueous solution at physiological pH. Complexes [Eu.1](+) and [Eu.3](+) bearing hydrogen bond donor groups in the pendant arms showed excellent discrimination between ATP, ADP and monophosphate species. Complex [Eu.3](+) showed relatively strong binding to ATP (logK (a)=5.8), providing a rapid, long‐lived luminescent signal that enabled its detection in a highly competitive aqueous medium containing biologically relevant concentrations of Mg(2+), ADP, GTP, UTP and human serum albumin. This Eu(III) complex responds linearly to ATP within the physiological concentration range (1–5 mm), and was used to continuously monitor the apyrase‐catalyzed hydrolysis of ATP to ADP in vitro. We demonstrate that [Eu.3](+) can permeate mammalian (NIH‐3T3) cells efficiently and localize to the mitochondria selectively, permitting real‐time visualization of elevated mitochondrial ATP levels following treatment with a broad spectrum kinase inhibitor, staurosporine, as well as depleted ATP levels upon treatment with potassium cyanide under glucose starvation conditions. John Wiley and Sons Inc. 2018-06-28 2018-07-25 /pmc/articles/PMC6175470/ /pubmed/29761917 http://dx.doi.org/10.1002/chem.201801008 Text en © 2018 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/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Mailhot, Romain Traviss‐Pollard, Thomas Pal, Robert Butler, Stephen J. Cationic Europium Complexes for Visualizing Fluctuations in Mitochondrial ATP Levels in Living Cells |
title | Cationic Europium Complexes for Visualizing Fluctuations in Mitochondrial ATP Levels in Living Cells |
title_full | Cationic Europium Complexes for Visualizing Fluctuations in Mitochondrial ATP Levels in Living Cells |
title_fullStr | Cationic Europium Complexes for Visualizing Fluctuations in Mitochondrial ATP Levels in Living Cells |
title_full_unstemmed | Cationic Europium Complexes for Visualizing Fluctuations in Mitochondrial ATP Levels in Living Cells |
title_short | Cationic Europium Complexes for Visualizing Fluctuations in Mitochondrial ATP Levels in Living Cells |
title_sort | cationic europium complexes for visualizing fluctuations in mitochondrial atp levels in living cells |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175470/ https://www.ncbi.nlm.nih.gov/pubmed/29761917 http://dx.doi.org/10.1002/chem.201801008 |
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