One Way Traffic: Base-to-Backbone Hole Transfer in Nucleoside Phosphorodithioate.

The directionality of the hole-transfer processes between DNA backbone and base was investigated by using phosphorodithioate [P(S )=S] components. ESR spectroscopy in homogeneous frozen aqueous solutions and pulse radiolysis in aqueous solution at ambient temperature confirmed initial formation of G -P(S )=S. The ionization potential of G-P(S )=S was calculated to be slightly lower than that of guanine in 5'-dGMP. Subsequent thermally activated hole transfer from G to P(S )=S led to dithiyl radical (P-2S ) formation on the μs timescale. In parallel, ESR spectroscopy, pulse radiolysis, and density functional theory (DFT) calculations confirmed P-2S formation in an abasic phosphorodithioate model compound. ESR investigations at low temperatures and higher G-P(S )=S concentrations showed a bimolecular conversion of P-2S to the σ -σ* -bonded dimer anion radical [-P-2S 2S-P-] [ΔG (150 K, DFT)=-7.2 kcal mol ]. However, [-P-2S 2S-P-] formation was not observed by pulse radiolysis [ΔG° (298 K, DFT)=-1.4 kcal mol ]. Neither P-2S nor [-P-2S 2S-P-] oxidized guanine base; only base-to-backbone hole transfer occurs in phosphorodithioate.