Abstract
Substitution of thymidine by 5-bromouridine within DNA sensitizes the nucleic acid to radiation. We show here the ability of low-energy (<12 eV) electrons, abundantly produced along the ionization tracks, to effectively decompose the radiosensitizer via two main fragmentation channels to produce the bromine anion and the 5-bromouracil-yl anion, with a cross-section of 2×-10 -14 and 9×10 -16 cm 2, respectively. The formation of these negative fragments is accompanied by their corresponding reactive radicals, i.e., uracil-yl radical bound to the sugar moiety and 2-deoxyribose-yl radical, which are both considered as precursors for DNA strand breaks. © 2004 Elsevier B.V.
Original language | English |
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Pages (from-to) | 442-447 |
Number of pages | 6 |
Journal | Chemical Physics Letters |
Volume | 393 |
Issue number | 4-6 |
DOIs | |
Publication status | Published - 1 Aug 2004 |
Keywords
- uridine derivative
- 5 bromouridine
- bromine derivative
- DNA
- radical
- thymidine
- unclassified drug
- uracil