Abstract
The influence of incubation time and Fenton reagent concentrations was investigated on the oxidation of 2'-deoxyguanosine. The compounds identified and quantified, through use of an LC-MS/MS system, were 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) and 8,5'- cyclo-2'-deoxyguanosine (8,5'cyclodG) and the secondary oxidation products guanidinohydantoin and dehydro-guanidinohydantoin. 8-oxodG and 8,5'cyclodG formed very quickly, reaching a maximum rapidly, but with 8-oxodC a rapid decline occurred thereafter due to its further oxidation into the secondary products, which formed more slowly. Due to the better stability, 8,5'cyclodG correlated better with the general level of oxidation than 8-oxodG. The results emphasize the advantages of measuring other oxidation adducts than 8-oxodG atone.
| Original language | English |
|---|---|
| Pages (from-to) | 259-278 |
| Journal | Nucleosides, Nucleotides & Nucleic Acids |
| Volume | 25 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 2006 |
Subject classification (UKÄ)
- Industrial Biotechnology
Free keywords
- Fenton reaction
- hydrogen peroxide
- iron sulfate
- 8-oxo-7
- 8-dihydro-2 '-deoxyguanosine
- LC-MS/MS
- 8
- 5 '-cyclo-2
- '-deoxyguanosine
- guanidinohydantoin
- dehydro-guanidinohydantoin
- free radicals
- quantification
- of modified nucleosides
- hydroxyl radical
- modified nucleosides
- oxidative damage
- 2 '-deoxyguanosine
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