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Bibliographic Details
Main Authors: André L. Lopes, Fernanda M. Prado, Helena C. Junqueira, Marisa H. G. Medeiros, Graziella E Ronsein, Jean Cadet, Paolo Di Mascio
Format: Artículo Open Access
Published: Wiley 2025
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Online Access:https://onlinelibrary.wiley.com/doi/10.1111/php.70044
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  • Direct evidence of singlet molecular oxygen [O 2 ( 1 Δg )] production from UVA excited 6‐thioguanine André L. Lopes Fernanda M. Prado Helena C. Junqueira Marisa H. G. Medeiros Graziella E Ronsein Jean Cadet Paolo Di Mascio Photochemistry and Photobiology Abstract 6‐Thioguanine (6‐TGua) is one of the thiopurines used as a cytostatic drug. When internalized by cells, 6‐TGua is metabolized through the purine salvage pathway and readily incorporated into DNA. Patients treated with these thiopurines are more prone to develop squamous cell carcinoma of the skin. The absorbance spectrum of 6‐TGua, in contrast to guanine (Gua) or any other canonical base, has a maximum absorbance at 342 nm. Therefore, 6‐TGua undergoes photoexcitation upon exposure to UVA radiation, with maximum absorption at 340 nm. In this study, the used approach unequivocally demonstrates the generation and quenching of 1 O 2 by 6‐TGua via the direct spectroscopic detection of 1 O 2 monomol light emission at 1270 nm. Chemiluminescence‐based methods were employed for the determination of the 1 O 2 generation quantum yield (Φ 1 O 2 ) and the total 1 O 2 quenching rate constant (k t ). For the 1 O 2 quantum yield, we found values of 0.22 ± 0.03 for 6‐TGua and 0.12 ± 0.03 for 2′‐deoxy‐6‐thioguanosine (6‐TdGuo). These compounds presented k t values of 1.5 × 10 7  L mol −1  s −1 and 1.1 × 10 7  L mol −1  s −1 , respectively. Through the comparison of these values with the ones obtained for 2′‐deoxyguanosine (dGuo) and its oxidation product 8‐oxo‐7,8‐dihydro‐2′‐deoxyguanosine (8‐oxodGuo), we aim to provide new insights into the 6‐TGua‐containing DNA (DNA‐6‐TGua) reactivity towards 1 O 2 in a biological context. 10.1111/php.70044 http://creativecommons.org/licenses/by/4.0/