Recent years have witnessed an increase of the interest in the studies of the
interaction of electrons with biologically relevant molecules. This has been mainly
motivated by the seminal work, where it has been demonstrated that low energy
electrons can induce single and double strand breaks in DNA in the energy range
below the level of ionization. Since the damage profile as a function of electron
energy showed pronounced resonances it was proposed that resonant electron
capture could occur at particular molecular components of the DNA as the initial
step towards strand breaks. From a series of experiments on electron attachment
to DNA building blocks (nucleobases, the sugar moiety and the phosphate unit)
became obvious that they effectively capture electrons leading to the formation of
low energy resonances associated with the decomposition of the corresponding
molecule. Recent dissociative electron attachment experiments on an entire gas
phase nucleotide 2’-deoxycytidine-5´-monophosphate give also insight into the
molecular mechanism involved, which comprises both direct electron attachment
to the backbone and transfer of the excess electron from cytosine to the backbone
resulting in single strand breaks. The results further allow an estimate of the relative
contribution of these different mechanisms to single strand breaks.
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