Summary
A transforming DNA system has been used to study the effect of silver ion on the X-ray-induced inactivation of the functional ability of DNA. In N2 transforming DNA is sensitized to radiation by Ag+, with the maximum sensitization occurring at a ratio of one Ag+ added per DNA base. This response can be partially prevented by addition of ·OH scavengers. In O2 the transforming DNA is only slightly sensitized by Ag+ except at very high Ag+ concentrations. These results are interpreted in terms of the e−aq sequestration theory of radiation sensitization. Studies on the binding of Ag+ to DNA show that at the maximum sensitization in N2, there is one Ag+ bound per DNA base pair and that this binding is unaffected by ·OH scavengers, although radiation may change these binding properties. Steady-state radiation chemistry studies indicate a difference in the response of DNA-Ag+ complexes to irradiation in N2 and in O2. As with the transforming DNA studies, these can be interpreted in terms of the e−aq sequestration theory of radiation sensitization.