Tandem base lesions are generated by hydroxyl radical within isolated DNA in aerated aqueous solution

The hydroxyl radical-mediated formation of two tandem base lesions within DNA including N-(2-deoxy-beta-D-erythro-pentofuranosyl)formylamine-8-oxo-7,8-dihydro-2'-deoxyguanosine (d beta F-8-oxodGuo) and and 8-oxodGuo-d beta F is reported in this study. A specific enzymatic processing was developed to quantitatively release the tandem lesions as dinucleoside monophosphates from DNA. Then, the resulting hydrolyzed DNA samples were analyzed using liquid chromatography coupled to electrospray ionization tandem mass spectrometry. The simultaneous measurement of the two vicinal lesions was performed in the negative mode using the accurate and sensitive multiple reaction monitoring technique. For this purpose, two characteristic ions arising from the fragmentation of the pseudo-molecular ion [M - H](-) were monitored. Both d beta F-8-oxodGuo and 8-oxodGuo-d beta F damage were found to be generated in gamma-irradiated DNA as a significant fraction of (OH)-O-. radical-induced base damage. Interestingly, 8-oxodGuo-d beta F was produced in a much higher yield than the reversed sequence lesion. Indirect evidence is provided for the formation of other tandem lesions involving 8-oxodGuo, but that still remain to be fully identified. Insights into the mechanism of formation of the DNA damage were gained from several experiments including DNA photosensitization, gamma-irradiation in the presence of iron, and exposure to Fenton reagents. This allowed refinement of the proposed pathways for the formation of d beta F-8-oxodGuo and 8-oxodGuo-d beta F tandem base damage.