摘要
Mitochondrial superoxide (O-2(center dot-)) underlies much oxidative damage and redox signaling. Fluorescent probes can detect O-2(center dot-), 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(center dot-) probe, MitoNeoD, which can assess O-2(center dot-) changes in vivo by mass spectrometry and in vitro by fluorescence. MitoNeoD comprises a O-2(center dot-)-sensitive reduced phenanthridinium moiety modified to prevent DNA intercalation, as well as a carbon-deuterium bond to enhance its selectivity for O-2(center dot-) 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(center dot-) from isolated mitochondria to animal models, thus offering away to examine the many roles of mitochondrial O-2(center dot-) production in health and disease.
- 出版日期2017-10-19