Direct Spectroscopic Observation of 8-Oxo-7,8-dihydro-2‘-deoxyguanosine Radicals in Double-Stranded DNA Generated by One-Electron Oxidation at a Distance by 2-Aminopurine Radicals

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Abstract

Oligonucleotide duplexes (15-mers) containing 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxo-dG) and the base analogue 2-aminopurine (2AP) separated from one another by zero, two, or four thymidine residues on the same strand, were synthesized. Selective two-photon excitation of 2AP with intense 308 nm XeCl excimer laser pulses (fwhm = 12 ns, ∼80 mJ pulse-1 cm-2) gives rise to 2AP radical cations that, in turn, oxidize 8-oxo-dG at a distance. Transient absorption techniques allowed for the direct monitoring of the oxidant and product radical intermediates as a function of time on the 100 ns−1 ms time scale and revealed the existence of two-component oxidation kinetics. The evolution in time of the rapid component (100 ns) is attributed to the oxidation of 8-oxo-dG by the deprotonation product of 2AP•+, the neutral radical 2AP(−H)•. Only the slow, microsecond kinetic component was observed when the 8-oxo-dG and 2AP are separated by four thymidines. The rate constants of electron transfer are (3.8 ± 0.5) × 104 s-1 and (3.0 ± 0.5) × 103 s-1 in the case of two and four intervening thymidines, respectively. Because of the pKa properties of the donor/acceptor couples, this slow, 0.1−1000 μs time scale electron transfer at a distance from 8-oxo-dG to the 2AP(−H)• radicals, is likely to occur via a proton-coupled electron-transfer mechanism.

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