Radiation Research · 1994 · 13 citations · 14 references
Natural SciencesChemistryMolecular BiologyRadiation BiophysicsRadiation DetectionSpectroscopyPhotochemistryUltraviolet Radiation BiologyCyclobutane Pyrimidine DimersDna Adducts From Ultraviolet RadiationPyrimidine (6-4) Pyrimidone PhotoproductsUltraviolet Light ExposureUltraviolet-induced Dna DamageUv-induced Dna LesionsWavelength DependenceX-ray Irradiation
Solid thymidylyl-(3'-->5')-thymidine (dTpdT) was irradiated in a vacuum with monochromatic photons from 150 to 300 nm; the photoproducts were analyzed quantitatively by high-performance liquid chromatography. The results of the experiment were as follows: (1) above 210 nm the major photoproducts were three dithymine photodimers [the cis-syn and trans-syn cyclobutane thymine dimers and the thymine (6-4) photoproduct]; below 210 nm, they were three photodecomposition products (thymine, thymidine 5'-monophosphate and thymidine 3'-monophosphate). This shows that 210 nm is the wavelength at which the major photoproducts change from dithymine photodimers (far-UV type) to photodecomposition products (X-ray type). (2) The yields of the three dithymine photodimers had a similar wavelength dependence with each other: the yields had a peak at 260 nm and gradually decreased toward shorter wavelengths to 150 nm. (3) The yields of the three photodecomposition products also had a very similar wavelength dependence with each other: the yields increased exponentially with a decrease in the wavelength. (4) The average ratios of the yield of the (6-4) photoproduct to that of the cis-syn dimer were 0.30 between 170 and 220 nm, but 0.16 between 240 and 290 nm.
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The ultraviolet photochemistry of thymidylyl-(3′→5′)-thymidine
H. E. Johns, Mark Pearson, J. Leblanc et al. · Journal of Molecular Biology · 1964 · 192 citations
Optical and dielectric properties of DNA in the extreme ultraviolet
Takashi Inagaki, R. N. Hamm, E. T. Arakawa et al. · The Journal of Chemical Physics · 1974 · 168 citations · Full text