Photosensitization of 2’-deoxyadenosine-5’-monophosphate by pterina

GABRIELA PETROSELLI,; MARÍA DÁNTOLA,; FRANCO CABRERIZO; ALBERTO L. CAPPARELLI; CAROLINA LORENTE; ESTHER OLIVEROS; ANDRES THOMAS,

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

American Chemical Society

Año: 2007

0002-7863

Abstract: UV-A radiation (320-400 nm) induces damages to the DNA molecule and its components through different photosensitized reactions. Among these processes, photosensitized oxidations may occur through electron transfer or hydrogen abstraction (type I) and/or the production of singlet molecular oxygen (1O2) (type II). Pterins, heterocyclic compounds widespread in biological systems, participate in relevant biological processes and are able to act as photosensitizers. We have investigated the photosensitization of 2´-deoxyguanosine 5´-monophosphate (dGMP) by pterin (PT) in aqueous solution under UV-A irrradiation. Kinetic analysis was employed to evaluate the participation of both types of mechanism under different pH conditions. The rate constant of 1O2 total quenching (kt) by dGMP was determined by steady-state analysis of the 1O2 luminescence, whereas the rate constant of the chemical reaction between 1O2 and dGMP (kr) was evaluated from kinetic analysis of concentration profiles obtained by HPLC. The results show that the dominant mechanism for the photosensitization of dGMP by PT in alkaline media involves the reaction of dGMP with 1O2 produced by energy transfer from the PT triplet state to molecular oxygen (type II). In contrast, under acidic pH conditions, where PT and the guanine moiety of dGMP are not ionized, the main pathway for dGMP oxidation involves an initial electron transfer between dGMP and the PT triplet state (type II mechanism). The biological implications of the results obtained are also discussed. UV-A radiation (320-400 nm) induces damages to the DNA molecule and its components through different photosensitized reactions. Among these processes, photosensitized oxidations may occur through electron transfer or hydrogen abstraction (type I) and/or the production of singlet molecular oxygen (1O2) (type II). Pterins, heterocyclic compounds widespread in biological systems, participate in relevant biological processes and are able to act as photosensitizers. We have investigated the photosensitization of 2´-deoxyguanosine 5´-monophosphate (dGMP) by pterin (PT) in aqueous solution under UV-A irrradiation. Kinetic analysis was employed to evaluate the participation of both types of mechanism under different pH conditions. The rate constant of 1O2 total quenching (kt) by dGMP was determined by steady-state analysis of the 1O2 luminescence, whereas the rate constant of the chemical reaction between 1O2 and dGMP (kr) was evaluated from kinetic analysis of concentration profiles obtained by HPLC. The results show that the dominant mechanism for the photosensitization of dGMP by PT in alkaline media involves the reaction of dGMP with 1O2 produced by energy transfer from the PT triplet state to molecular oxygen (type II). In contrast, under acidic pH conditions, where PT and the guanine moiety of dGMP are not ionized, the main pathway for dGMP oxidation involves an initial electron transfer between dGMP and the PT triplet state (type II mechanism). The biological implications of the results obtained are also discussed. UV-A radiation (320-400 nm) induces damages to the DNA molecule and its components through different photosensitized reactions. Among these processes, photosensitized oxidations may occur through electron transfer or hydrogen abstraction (type I) and/or the production of singlet molecular oxygen (1O2) (type II). Pterins, heterocyclic compounds widespread in biological systems, participate in relevant biological processes and are able to act as photosensitizers. We have investigated the photosensitization of 2´-deoxyguanosine 5´-monophosphate (dGMP) by pterin (PT) in aqueous solution under UV-A irrradiation. Kinetic analysis was employed to evaluate the participation of both types of mechanism under different pH conditions. The rate constant of 1O2 total quenching (kt) by dGMP was determined by steady-state analysis of the 1O2 luminescence, whereas the rate constant of the chemical reaction between 1O2 and dGMP (kr) was evaluated from kinetic analysis of concentration profiles obtained by HPLC. The results show that the dominant mechanism for the photosensitization of dGMP by PT in alkaline media involves the reaction of dGMP with 1O2 produced by energy transfer from the PT triplet state to molecular oxygen (type II). In contrast, under acidic pH conditions, where PT and the guanine moiety of dGMP are not ionized, the main pathway for dGMP oxidation involves an initial electron transfer between dGMP and the PT triplet state (type II mechanism). The biological implications of the results obtained are also discussed.