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MitoNeoD: A Mitochondria-Targeted Superoxide Probe

  • Maria M. Shchepinova
  • , Andrew G. Cairns
  • , Tracy A. Prime
  • , Angela Logan
  • , Andrew M. James
  • , Andrew R. Hall
  • , Sara Vidoni
  • , Sabine Arndt
  • , Stuart T. Caldwell
  • , Hiran A. Prag
  • , Victoria R. Pell
  • , Thomas Krieg
  • , John F. Mulvey
  • , Pooja Yadav
  • , James N. Cobley
  • , Thomas P. Bright
  • , Hans M. Senn
  • , Robert F. Anderson
  • , Michael P. Murphy
  • , Richard C. Hartley

نتاج البحث: Articleمراجعة النظراء

94 اقتباسات (Scopus)
205 التنزيلات (Pure)

ملخص

Mitochondrial superoxide (O2⋅−) underlies much oxidative damage and redox signaling. Fluorescent probes can detect O2⋅−, 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 O2⋅− probe, MitoNeoD, which can assess O2⋅− changes in vivo by mass spectrometry and in vitro by fluorescence. MitoNeoD comprises a O2⋅−-sensitive reduced phenanthridinium moiety modified to prevent DNA intercalation, as well as a carbon-deuterium bond to enhance its selectivity for O2⋅− 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 O2⋅− from isolated mitochondria to animal models, thus offering a way to examine the many roles of mitochondrial O2⋅− production in health and disease.
اللغة الأصليةEnglish
الصفحات (من إلى)1285-1298.e12
دوريةCell Chemical Biology
مستوى الصوت24
رقم الإصدار10
المعرِّفات الرقمية للأشياء
حالة النشرPublished - 1 أكتوبر 2017

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