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1.
Org Biomol Chem ; 8(14): 3211-9, 2010 Jul 21.
Artículo en Inglés | MEDLINE | ID: mdl-20502776

RESUMEN

The present work is aimed at gaining conclusive mechanistic insights into the radiation-induced formation of the 5'R and 5'S diastereomers of both adenine and guanine 5',8-cyclo-2'-deoxyribonucleosides, with emphasis on the delineation of the inhibitory effect of O(2) in isolated and cellular DNA. The levels of purine 5',8-cyclo-2'-deoxyribonucleosides as assessed by HPLC-MS/MS were found to decrease steadily with the increase of O(2) concentration, the 5',8-cyclo-2'-deoxyguanosine being produced more efficiently than the 5',8-cyclo-2'-deoxyadenosine for low O(2) concentrations. A high stereoselectivity was observed in the intramolecular addition of the C5' radical to the C8 of the purine leading, after the creation of the C5'-C8 bond and a subsequent oxidation step, to the predominant formation of the 5'R diastereomer for both purine 5',8-cyclonucleosides. The reduced formation yield of the 4 tandem lesions in the presence of O(2) explains, at least partly, the low efficiency of radiation-induced yields of the purine 5',8-cyclo-2'-deoxyribonucleosides in cellular DNA, which are about two orders of magnitude lower than the previously reported data obtained from HPLC-MS analysis.


Asunto(s)
ADN/metabolismo , Rayos gamma , Oxígeno/farmacología , Nucleósidos de Purina/metabolismo , Animales , Bovinos , Ciclización , ADN/genética , Daño del ADN , Reparación del ADN/efectos de los fármacos , Reparación del ADN/efectos de la radiación , Humanos , Radical Hidroxilo/metabolismo , Modelos Moleculares , Conformación Molecular , Monocitos/metabolismo , Monocitos/efectos de la radiación , Nucleósidos de Purina/química , Estereoisomerismo , Especificidad por Sustrato , Agua/química
2.
Org Lett ; 10(20): 4409-12, 2008 Oct 16.
Artículo en Inglés | MEDLINE | ID: mdl-18808126

RESUMEN

Photolysis of the title dyads under aerobic conditions leads to a 2-deoxyribonolactone derivative. Laser flash photolysis reveals that the process occurs from the short-lived benzophenone-like triplet excited state. A mechanism involving intramolecular electron transfer with the purine bases (adenine, guanine, or 8-oxoadenine) as donors is proposed.


Asunto(s)
Benzofenonas/química , Cetonas/química , Purinas/química , Azúcares Ácidos/síntesis química , Radicales Libres/química , Estructura Molecular , Fotoquímica , Espectrofotometría , Azúcares Ácidos/química
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