Pulse Radiolytic Study of the Interaction of SO⁻·₄ with Deoxynucleosides. Possible Implications for Direct Energy Deposition

References

• Adams G.E., Cooke M.S. Electron-affinic sensitization. I. A structural basis for chemical radiosensitizers in bacteria. International Journal of Radiation Biology 1969; 15: 457–471
   Web of Science ®Google Scholar
• Al-Sheikhly M., von Sonntag C. γ-Radiolysis of 1,3-dimethyluracil in N2O-saturated aqueous solutions. Zeitschrift für Naturforschung 1983; 38b: 1622–1629
   Google Scholar
• Bansal M.K., Fessenden R.W. Radiation-chemical studies of the reaction of SO-4 with uracil and its derivatives. Radiation Research 1978; 75: 497–507
   Web of Science ®Google Scholar
• Boon P.J., Cullis P.M., Symons M.C.R., Wren B.W. Effects of ionizing radiation on deoxyribonucleic acid and related systems, Part I. The role of oxygen. Journal of the Chemical Society, Perkin Transactions II 1984; 1393–1399
   Google Scholar
• Cullis P.M., Symons M.C.R. Effects of direct radiation on deoxyribonucleic acid. Radiation Physics and Chemistry 1986; 27: 93–100
   Web of Science ®Google Scholar
• Deeble D.J., von Sonntag C. The UV absorption spectra of the C(5) and C(6) OH adduct radicals of uracil and thymine derivatives. A pulse radiolysis study. Zeitschrift für Naturforschung 1985; 40c: 925–928
   Google Scholar
• Eibenberger H., Steenken S., O'Neill P., Schulte-Frohlinde D. Pulse radiolysis and electron spin resonance studies concerning the reaction of SO-4 with alcohols and ethers in aqueous solution. Journal of Physical Chemistry 1978; 82: 749–750
   Google Scholar
• Fujita S. Radiolysis of nucleosides in aqueous solution: base liberation by the base attack mechanism. International Journal of Radiation Biology 1984; 45: 371–377
   Web of Science ®Google Scholar
• Fujita S., Steenken S. Pattern of OH radical addition to uracil and methyl- and carboxyl-substituted uracils. Electron transfer of OH adducts with N,N,N′,N′-tetramethyl-p-phenylenediamine and tetranitromethane. Journal of the American Chemical Society 1981; 103: 2540–2545
   Web of Science ®Google Scholar
• Goodhead D. Cellular effects of ultrasoft X-radiation: implications for mechanism of radiation cell killing. The Biological Basis of Radiotherapy, G.G. Steel, G.E. Adams, M. Peckham. Elsevier, Amsterdam 1983; 81–92
   Google Scholar
• Gräslund A., Ehrenberg A., Rupprecht A., Ström G., Crespi H. Ionic base radicals in γ-irradiated oriented non-deuterated and fully-deuterated DNA. International Journal of Radiation Biology 1975; 28: 313–323
   Web of Science ®Google Scholar
• Gräslund A., Ehrenberg A., Rupprecht A. Free-radical formation in γ-irradiated oriented DNA containing electron-affinic radiosensitizers. International Journal of Radiation Biology 1977; 31: 145–152
   Web of Science ®Google Scholar
• Gräslund A., Rupprecht A., Köhnlein W., Hüttermann J. Radiation-induced free radicals in oriented bromouracil-substituted DNA. Radiation Research 1981; 88: 1–10
   PubMed Web of Science ®Google Scholar
• Gregoli S., Olast M., Bertinchamps A. Radiolytic pathways in γ-irradiated DNA: influence of chemical and conformational factors. Radiation Research 1982; 89: 238–254
   PubMed Web of Science ®Google Scholar
• Gurzadyan G.G., Nikogosyan D.N., Balmukhanov T.S., Zavilgelskij G.B. The study of formation of single-strand breaks in the DNA chain under picosecond laser UV irradiation. Photobiochemistry and Photobiophysics 1982; 4: 87–94
   Google Scholar
• Hayon E., Simic M. Addition of hydroxyl radicals to pyrimidine bases and electron transfer reactions of intermediates. Journal of the American Chemical Society 1973; 95: 1029–1035
   PubMed Web of Science ®Google Scholar
• Hayon E., Treinin A., Wilf J. Electronic spectra, photochemistry and autooxidation mechanisms of the sulfite-bisulfite-pyrosulfite systems. The SO-2, SO-3, SO-4 and SO-5 radicals. Journal of the American Chemical Society 1972; 94: 47–57
   Web of Science ®Google Scholar
• Hazra D.K., Steenken S. Pattern of OH radical addition to cytoxine and 1-, 3-, 5- and 6-substituted cytosine. Electron transfer and dehydration reactions of the OH adducts. Journal of the American Chemical Society 1983; 105: 4380–4386
   Web of Science ®Google Scholar
• Heckel E., Henglein A., Beck G. Pulsradiolytische Untersuchung des Radikalanions SO-4. Berichte der Bunsengesellschaft für Physikalische Chemie 1966; 70: 149–154
   Google Scholar
• Hissung A., von Sonntag C. Radiolysis of cytosine, 5-methyl cytosine and 2′-deoxycytidine in deoxygenated aqueous solution. A pulse spectroscopic and pulse conductometric study of the OH adduct. Zeitschrift für Naturforschung 1978; 33b: 321–328
   Google Scholar
• Effects of Ionizing Radiation in DNA, J. Hüttermann, W. Köhnlein, R. Teoule, A.J. Bertichamps. Spinger Verlag, Berlin 1978
   Google Scholar
• Hüttermann J., Voit K., Oloff H., Köhnlein W., Gräsland A., Rupprecht A. Specific formation of electron gain and loss centres in X-irradiated oriented fibres of DNA at low temperatures. Faraday Discussions of the Chemical Society 1984; 78: 135–149
   Google Scholar
• Jovanovic S.V., Simic M.G. One-electron redox potentials of purines and pyrimidines. Journal of Physical Chemistry 1986a; 90: 974–978
   Web of Science ®Google Scholar
• Jovanovic S.V., Simic M.G. Mechanisms of OH-radical reactions with thymine and uracil derivatives. Journal of the American Chemical Society 1986b; 108: 5968–5972
   PubMed Web of Science ®Google Scholar
• Lith D. van, de Haas M.P., Warman J.M., Hummel A. Highly mobile charge carriers in hydrated DNA and collagen formed by pulsed ionization. Biopolymers 1983; 22: 807–810
   PubMed Web of Science ®Google Scholar
• Lith D. van, Warman J.M., de Haas M.P., Hummel A. Electron migration in hydrated DNA and collagen at low temperatures. Part 1: Effect of water concentration. Journal of the Chemical Society, Faraday Transactions 1 1986a; 82: 2933–2943
   Web of Science ®Google Scholar
• Lith D. van, Eden J., Warman J.M., Hummel A. Electron migration in hydrated DNA and collagen at low temperatures. Part 2: The effect of additives. Journal of the Chemical Society, Faraday Transactions 1 1986b; 82: 2945–2950
   Web of Science ®Google Scholar
• Michaels H.B., Hunt J.W. Reactions of the hydroxyl radical with polynucleotides. Radiation Research 1973; 56: 57–70
   PubMed Web of Science ®Google Scholar
• O'Neill P. Pulse radiolytic study of the interaction of thiols and ascorbate with OH-adducts of dGMP and dG: Implications for DNA repair processes. Radiation Research 1983; 96: 198–210
   PubMed Web of Science ®Google Scholar
• O'Neill P. Hydroxyl radical damage: potential repair by sulphydryls, ascorbate, and other anti-oxidants. Life Chemistry Reports 1984; 1: 337–341
   Google Scholar
• O'Neill P., Chapman P.W. Potential repair of free radical adducts of dGMP and dG by a series of reductants. A pulse radiolytic study. International Journal of Radiation Biology 1985; 47: 71–80
   Web of Science ®Google Scholar
• O'Neill P., Chapman P.W., Papworth D.G. Repair of hydroxyl radical damage of dA by antioxidants. Life Chemistry Reports 1985; 3: 62–69
   Google Scholar
• O'Neill P., Davies S.E. Interaction of peroxyl radical adducts of DNA bases with reductants. Superoxide and Superoxide Dismutase in Chemistry, Biology and Medicine, G. Rotilio. Elsevier, Amsterdam 1986a; 44–46
   Google Scholar
• O'Neill P., Davies S.E. A pulse radiolytic study of the interaction of nitroxyls with free radical adducts of purines: consequences for radiosensitisation. International Journal of Radiation Biology 1986b; 49: 937–950
   Web of Science ®Google Scholar
• O'Neill P., Fielden E.M. Molecular aspects of DNA damage and its modification. Radiation Carcinogenesis and DNA Alterations, F.J. Burns, A.C. Upton, G. Silini. Plenum, New York 1986; 425–438
   Google Scholar
• O'Neill P., Steenken S., Schulte-Frohlinde D. Formation of radical cations of methoxylated benzenes by reaction with OH radicals, Tl2+, Ag2+, and SO-4 in aqueous solution. An optical and conductometric pulse radiolysis and in situ radiolysis electron spin resonance study. Journal of Physical Chemistry 1975; 79: 2773–2779
   Web of Science ®Google Scholar
• Roebke W., Renz M., Henglein A. Pulsradiolyse der Anionen S2O2-8 und HSO-5 in wässriger Lösung. International Journal of Radiation Physics and Chemistry 1969; 1: 39–44
   Google Scholar
• Ross A.B., Neta P. Rate constants for reactions of inorganic radicals in aqueous solution. National Bureau of Standards, Washington D.C. 1979, NSRDS-NBS65
   Google Scholar
• Rustgi S.N., Riesz P. An esr and spin-trapping study of the reactions of the SO-4 radical with protein and nucleic acid constituents. International Journal of Radiation Biology 1978; 34: 301–316
   Web of Science ®Google Scholar
• Schuchmann P.H., Deeble D.J., Olbrich G., von Sonntag C. The SO-4-induced chain reaction of 1,3-dimethyluracil with peroxodisulphate. International Journal of Radiation Biology 1987; 57: 441–453
   Google Scholar
• Schulte-Frohlinde D. Kinetics and mechanism of polynucleotide and DNA strand break formation. Radioprotectors and Anticarcinogens, O.F. Nygaard, M.G. Simic. Academic Press, New York 1983; 53–71
   Google Scholar
• Schulte-Frohlinde D., Opitz J., Görner H., Bothe E. Model studies for the direct effect of high-energy irradiation on DNA. Mechanism of strand break formation induced by laser photoionization of poly U in aqueous solution. International Journal of Radiation Biology 1985; 48: 397–408
   Web of Science ®Google Scholar
• Schwarz H.A., Dodson R.W. Equilibrium between hydroxyl radicals and thallium (II) and the oxidation potential of OH (aq). Journal of Physical Chemistry 1984; 88: 3643–3647
   Web of Science ®Google Scholar
• Sevilla M.D. Mechanisms of radiation damage in DNA constituents and DNA. Excited States in Organic Chemistry and Biochemistry, B. Pullman, N. Goldblum. Reidel, Dordrecht 1977; 15–25
   Google Scholar
• von Sonntag C. Carbohydrate radicals: from ethylene glycol to DNA strand breakage. International Journal of Radiation Biology 1984; 46: 507–519
   Web of Science ®Google Scholar
• von Sonntag C. New aspects in the free-radical chemistry of pyrimidine nucleobases. Free Radical Research Communications 1987; 2: 217–224
   PubMedGoogle Scholar
• Ward J.F. Some biochemical consequences of the spatial distribution of ionizing radiation-produced free radicals. Radiation Research 1981; 86: 185–195
   PubMed Web of Science ®Google Scholar
• Ward J.F. Mammalian cells are not killed by DNA single strand breaks caused by hydroxyl radicals from hydrogen peroxide. Radiation Research 1985; 103: 383–392
   PubMed Web of Science ®Google Scholar
• Willson R.L. The reaction of oxygen with radiation-induced free radicals of DNA and related compounds. International Journal of Radiation Biology 1970; 17: 349–358
   Web of Science ®Google Scholar
• Willson R.L., Wardman P., Asmus K.-D. Interaction of dGMP radical with cysteamine and promethazine as possible model of DNA repair. Nature 1974; 252: 323–324
   PubMed Web of Science ®Google Scholar
• Wold E., Brustad T. Reactions between nitroxyl free radicals and radiation-induced transients in nucleosides. International Journal of Radiation Biology 1973; 24: 153–160
   Web of Science ®Google Scholar
• Woodruff W.H., Margerum D.W. Thermodynamical parameters of aqueous halogen radicals. Inorganic Chemistry 1973; 12: 962–964
   Web of Science ®Google Scholar