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MitoNeoD: A Mitochondria-Targeted Superoxide Probe
Mitochondrial superoxide (O(2)(⋅−)) underlies much oxidative damage and redox signaling. Fluorescent probes can detect O(2)(⋅−), but are of limited applicability in vivo, while in cells their usefulness is constrained by side reactions and DNA intercalation. To overcome these limitations, we develop...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278870/ https://www.ncbi.nlm.nih.gov/pubmed/28890317 http://dx.doi.org/10.1016/j.chembiol.2017.08.003 |
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author | Shchepinova, Maria M. Cairns, Andrew G. Prime, Tracy A. Logan, Angela James, Andrew M. Hall, Andrew R. Vidoni, Sara Arndt, Sabine Caldwell, Stuart T. Prag, Hiran A. Pell, Victoria R. Krieg, Thomas Mulvey, John F. Yadav, Pooja Cobley, James N. Bright, Thomas P. Senn, Hans M. Anderson, Robert F. Murphy, Michael P. Hartley, Richard C. |
author_facet | Shchepinova, Maria M. Cairns, Andrew G. Prime, Tracy A. Logan, Angela James, Andrew M. Hall, Andrew R. Vidoni, Sara Arndt, Sabine Caldwell, Stuart T. Prag, Hiran A. Pell, Victoria R. Krieg, Thomas Mulvey, John F. Yadav, Pooja Cobley, James N. Bright, Thomas P. Senn, Hans M. Anderson, Robert F. Murphy, Michael P. Hartley, Richard C. |
author_sort | Shchepinova, Maria M. |
collection | PubMed |
description | Mitochondrial superoxide (O(2)(⋅−)) underlies much oxidative damage and redox signaling. Fluorescent probes can detect O(2)(⋅−), but are of limited applicability in vivo, while in cells their usefulness is constrained by side reactions and DNA intercalation. To overcome these limitations, we developed a dual-purpose mitochondrial O(2)(⋅−) probe, MitoNeoD, which can assess O(2)(⋅−) changes in vivo by mass spectrometry and in vitro by fluorescence. MitoNeoD comprises a O(2)(⋅−)-sensitive reduced phenanthridinium moiety modified to prevent DNA intercalation, as well as a carbon-deuterium bond to enhance its selectivity for O(2)(⋅−) over non-specific oxidation, and a triphenylphosphonium lipophilic cation moiety leading to the rapid accumulation within mitochondria. We demonstrated that MitoNeoD was a versatile and robust probe to assess changes in mitochondrial O(2)(⋅−) from isolated mitochondria to animal models, thus offering a way to examine the many roles of mitochondrial O(2)(⋅−) production in health and disease. |
format | Online Article Text |
id | pubmed-6278870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62788702018-12-13 MitoNeoD: A Mitochondria-Targeted Superoxide Probe Shchepinova, Maria M. Cairns, Andrew G. Prime, Tracy A. Logan, Angela James, Andrew M. Hall, Andrew R. Vidoni, Sara Arndt, Sabine Caldwell, Stuart T. Prag, Hiran A. Pell, Victoria R. Krieg, Thomas Mulvey, John F. Yadav, Pooja Cobley, James N. Bright, Thomas P. Senn, Hans M. Anderson, Robert F. Murphy, Michael P. Hartley, Richard C. Cell Chem Biol Article Mitochondrial superoxide (O(2)(⋅−)) underlies much oxidative damage and redox signaling. Fluorescent probes can detect O(2)(⋅−), but are of limited applicability in vivo, while in cells their usefulness is constrained by side reactions and DNA intercalation. To overcome these limitations, we developed a dual-purpose mitochondrial O(2)(⋅−) probe, MitoNeoD, which can assess O(2)(⋅−) changes in vivo by mass spectrometry and in vitro by fluorescence. MitoNeoD comprises a O(2)(⋅−)-sensitive reduced phenanthridinium moiety modified to prevent DNA intercalation, as well as a carbon-deuterium bond to enhance its selectivity for O(2)(⋅−) over non-specific oxidation, and a triphenylphosphonium lipophilic cation moiety leading to the rapid accumulation within mitochondria. We demonstrated that MitoNeoD was a versatile and robust probe to assess changes in mitochondrial O(2)(⋅−) from isolated mitochondria to animal models, thus offering a way to examine the many roles of mitochondrial O(2)(⋅−) production in health and disease. Cell Press 2017-10-19 /pmc/articles/PMC6278870/ /pubmed/28890317 http://dx.doi.org/10.1016/j.chembiol.2017.08.003 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shchepinova, Maria M. Cairns, Andrew G. Prime, Tracy A. Logan, Angela James, Andrew M. Hall, Andrew R. Vidoni, Sara Arndt, Sabine Caldwell, Stuart T. Prag, Hiran A. Pell, Victoria R. Krieg, Thomas Mulvey, John F. Yadav, Pooja Cobley, James N. Bright, Thomas P. Senn, Hans M. Anderson, Robert F. Murphy, Michael P. Hartley, Richard C. MitoNeoD: A Mitochondria-Targeted Superoxide Probe |
title | MitoNeoD: A Mitochondria-Targeted Superoxide Probe |
title_full | MitoNeoD: A Mitochondria-Targeted Superoxide Probe |
title_fullStr | MitoNeoD: A Mitochondria-Targeted Superoxide Probe |
title_full_unstemmed | MitoNeoD: A Mitochondria-Targeted Superoxide Probe |
title_short | MitoNeoD: A Mitochondria-Targeted Superoxide Probe |
title_sort | mitoneod: a mitochondria-targeted superoxide probe |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278870/ https://www.ncbi.nlm.nih.gov/pubmed/28890317 http://dx.doi.org/10.1016/j.chembiol.2017.08.003 |
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