2-Deoxyribonolactone lesions were identified as major products of radiation damage to DNA mediated by o,o'-diphenyleneiodonium cations in a hydroxyl radical-scavenging environment. The highest selectivity toward deoxyribonolactone formation (up to 86% of all sugar-phosphate damages) and the overall reaction efficiency (up to 40% of all radiation-generated intermediates converted into products) was displayed by derivatives with positively charged (2-aminoethylthio)acetylamino and (2-aminoethylamino)acetylamino side chains. The reaction can be useful for random single-step incorporation of deoxyribonolactone lesions into single- and double-stranded oligonucleotides and highly polymerized DNA directly in commonly used buffers (PBS, phosphate, Tris-HCl, etc.) at room temperature. In combination with HPLC separation, this technique can serve as a source of short (<6 mer) sequences containing deoxyribonolactone lesions at known positions. (C) 2009 be Radiation Research Society
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East Tennessee State Univ, Dept Phys & Astron, Box 70652, Johnson City, TN 37614 USAEast Tennessee State Univ, Dept Phys & Astron, Box 70652, Johnson City, TN 37614 USA
Razskazovskiy, Yuriy
Tegomoh, Modeste
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East Tennessee State Univ, Dept Chem, Johnson City, TN 37614 USA
Tempur Ped Technol Inc, TEMPUR SEALY, 203 Tempur Ped Dr,Suite 102, Duffield, VA 24244 USAEast Tennessee State Univ, Dept Phys & Astron, Box 70652, Johnson City, TN 37614 USA
Tegomoh, Modeste
Roginskaya, Marina
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East Tennessee State Univ, Dept Chem, Johnson City, TN 37614 USAEast Tennessee State Univ, Dept Phys & Astron, Box 70652, Johnson City, TN 37614 USA