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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 |
Sumario: | 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. |
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