Direct ionization of DNA creates sites of electron loss and electron gain in DNA. The former, referred to as radical cations or holes, are initially distributed between the deoxyribose-phosphate backbone and the four bases in accordance with the number of electrons per constituent (the Bragg rule). The holes are either trapped at the initial site of ionization or migrate short distances before being trapped; in either case, deprotonation is the key trapping event (1, 2). The redistributed holes are trapped selectively, primarily by deoxyribose and the guanine base, and the sites of electron gain (radical anions) are predominantly pyrimidines (3, 4). These one-electron transfer reactions are summarized in reactions (1-3), and the free radical structures, except for dRib(Cn′-H)•, are given in Scheme 1. dRib(Cn′-H)• represents any of the five deoxyribose radicals formed by a net loss hydrogen from one of the five deoxyribose carbons; in Scheme 1, an example is given for the C1′ radical, dRib(C1′-H)•.