Abstract
–The use of absorption and fluorescence spectroscopy for following the progress of the photo‐reaction between DNA and 4′‐aminomethyl‐4,5′,8‐trimethylpsoralen (AMT) has been investigated. Absorption at long wavelengths and fluorescence both decline upon intercalation of AMT into the DNA helix. The loss of fluorescence from AMT and the accompanying appearance of monoadduct fluorescence upon irradiation by UV light can be easily followed by using the excitation beam of a spectro‐fluorometer as the source of irradiation and monitoring the changing emission spectrum. Where cross‐link formation is possible, the subsequent decline of monoadduct fluorescence is seen as well. This suggests that the 4,5‐tnonoadduct is a precursor of cross‐links. Both monoaddition and cross‐linking are more rapid with poly d(A·T) than with calf thymus DNA or poly d(A·T). Excitation spectra can be helpful in resolving the levels of AMT and 4′,5′‐monoadduct when both are contributing to the emission spectrum. Some changes are observed in the emission spectrum of AMT–poly d(A·T) monoadducts after prolonged irradiation which indicate further photoreaction.