DNA photodamage: Study of cyclobutane pyrimidine dimer formation in a locked thymine dinucleotide. Issue 3 (2010)

• Record Type: Journal Article
• Authors: Schreier Schreier, W. J. W. J.; Kubon Kubon, J. J.; Clivio Clivio, P. P.; Zinth Zinth, W. W.; Gilch Gilch, P. P.
• Is Part Of: Spectroscopy. Volume 24:Issue 3/4(2010)
• Page Start: 309
• Page End: 316
• Publication Date: 2010
• Subjects: Infrared spectroscopy -- DNA photolesion -- CPD damage -- thymine dimer
• DOI: 10.3233/SPE-2010-0437
• Languages: English
• ISSNs: 0712-4813

Abstract

Abstract : The cyclobutane pyrimidine dimer (CPD) formed between two adjacent thymine bases is the most abundant DNA photolesion induced by UV radiation. The quantum yield of this reaction is on the order of ~1% in DNA. This small quantum yield hampers the study of damage formation in naturally occurring DNA. Investigations with increased accuracy become possible for a locked nucleotide model compound TL pTL which exhibits a quantum yield of about 10% for CPD formation. Time resolved IR spectroscopy on TL pTL and two other DNA model compounds (TpT and (dT)18 ) reveals that: (i) The absorption changes after ~1 ps are due to CPD photodamage. (ii) The quantum efficiency of CPD formation on the few picosecond time scale equals the quantum efficiency reported in stationary experiments. CPD photodamage formation in the investigated DNA constructs is thus predominantly formed from the primarily photoexcited singlet ππ* state, whereas the triplet channel does not play an essential role.