Abstract
Some aspects of the interactions between DNA and 8-methoxypsoralen (8-MOP) in its ground state (complex formation) or in its excited state (photobinding) have been investigated. 8-MOP shows a low affinity towards DNA in the complex formation; this fact minimizes the possible biological consequences deriving from this interaction, when it occurs in vivo. In covalent photobinding to DNA, 8-MOP forms mainly monofunctional adducts, and to a lesser extent bifunctional adducts, showing a behavior similar to that of other linearly condensed furocoumarins (psoralens); the ratio between mono-and bifunctional adducts was found to be 9:1. The covalent photobinding to DNA does not occur at random along the macromolecule, but preferentially at the level of specific receptor sites. The regions having an alternate sequence of A-T seem to be the best receptor sites for the formation of monoadducts while the regions containing an alternate sequence of A-T and C-G appeared to be the preferential sites for the cross-linkage formation.
Cite
CITATION STYLE
Dall’Acqua, F., Vedaldi, D., Bordin, F., & Rodighiero, G. (1979). New studies on the interaction between 8-methoxypsoralen and DNA in vitro. Journal of Investigative Dermatology, 73(2), 191–197. https://doi.org/10.1111/1523-1747.ep12581681
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.