Synthesis of 8-oxo-7,8-dihydro-2'-deoxyguanosine from 2'-deoxyguanosine using Cu(II)/H2O2/ascorbate: A new strategy for an improved yield

Biotechniques. 2016 Jun 1;60(6):279-84. doi: 10.2144/000114424. eCollection 2016.

Abstract

The free nucleoside 2'-deoxyguanosine (dGuo) is the most susceptible to oxidation by reactive oxygen species (ROS) compared to the other free nucleosides, and its oxidation product 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodGuo) has been used as a biomarker to quantify oxidative stress damage. We investigated different reactions using Fe(2+) or Cu(2+) and H2O2 in order to identify the reaction with the best yield. HPLC coupled with a UV detector and micrOTOF mass spectrometry were used to detect and confirm the identity of 8-oxodGuo. The optimized reaction synthesized 8-oxodGuo with a yield of 72.0%, much higher than that previously described in the literature. Our improved method for 8-oxodGuo synthesis could be extremely useful for assays that require the synthesis of internal standards labeled with stable isotopes.

Keywords: 8-oxodGuo; DNA damage; Fenton reaction; dGuo; synthesis.

MeSH terms

  • 8-Hydroxy-2'-Deoxyguanosine
  • Ascorbic Acid / chemistry*
  • Chromatography, High Pressure Liquid
  • Copper / chemistry*
  • Deoxyguanosine / analogs & derivatives*
  • Deoxyguanosine / chemical synthesis
  • Deoxyguanosine / chemistry*
  • Deoxyguanosine / isolation & purification
  • Hydrogen Peroxide / chemistry*
  • Iron / chemistry
  • Mass Spectrometry
  • Metals / chemistry
  • Spectrophotometry, Ultraviolet

Substances

  • Metals
  • Copper
  • 8-Hydroxy-2'-Deoxyguanosine
  • Hydrogen Peroxide
  • Iron
  • Deoxyguanosine
  • Ascorbic Acid