Fluorescent molecular rotors detect O6-methylguanine dynamics and repair in duplex DNA

Alkylation at the O-6 position of guanine is a common and highly mutagenic form of DNA damage. Direct repair of O-6-alkylguanines by the "suicide" enzyme O6-methylguanine DNA methyltransferase (MGMT, AGT, AGAT) maintains genome stability and inhibits carcinogenesis. In this study, a fluorescent analogue of thymidine containing trans-stilbene (T-ts) is quenched by O-6-methylguanine residues in the opposite strand of DNA by molecular dynamics that propagate through the duplex with as much as similar to 9 angstrom of separation. Increased fluorescence of T-ts or the cytosine analogue C-ts resulting from MGMT-mediated DNA repair were distinguishable from non-covalent DNA-protein binding following protease digest. To our knowledge, this is the first study utilizing molecular rotor base analogues to detect DNA damage and repair activities in duplex DNA.