Vendrell Criado, VictoriaRodríguez Muñiz, Gemma MaríaLhiaubet, Virginie LyriaCuquerella Alabort, Maria ConsueloMiranda Alonso, Miguel Ángel2018-02-182018-02-182016https://riunet.upv.es/handle/10251/98042[EN] Based on our previous investigations into the photophysical properties of the 5-methyl-2-pyrimidone (Pyo) chromophore, we now extend our studies to the photobehavior of the dimeric (6-4) thymine photoproducts (6-4 PP) to evaluate their capability to act as instrinsic DNA photosensitizers. The lesion presents significant absorption in the UVB/UVA region, weak fluorescence emission, a singlet-excited-state energy of approximately 351 kJ mol(-1), and a triplet-excited-state energy of 297 kJ mol(-1). Its triplet transient absorption has a maximum at 420-440 nm, a lifetime of around 7 mu s, and a high formation quantum yield, Phi(ISC) = 0.86. This species is efficiently quenched by thymidine. Its DNA photosensitizing properties are demonstrated by a series of experiments run on a pBR322 plasmid. The lesion photoinduces both single-strand breaks and the formation of cyclobutane thymine dimers. Altogether, these results show that, the substitution of the pyrimidone ring at C4 by a 5-hydroxy-5,6-dihydrothymine does not cancel out the photosensitization properties of the chromophore.Reserva de todos los derechosCyclobutane pyrimidine dimersDNA damagePhotochemistryPyrimidoneTriplet excited statesQUIMICA ORGANICAQUIMICA ANALITICAArtículo10.1002/cphc.201600154Abierto1439-764126990589