Conformation-specific recognition of carcinogen-DNA adduct in Escherichia coli nucleotide excision repair
Date of Original Version
We report a systematic and quantitative structure-function relationship study of the major N-[deoxyguanosin-8-yl]-2-aminofluorene adduct (AF) derived from the prototype carcinogen 2-aminofluorene and its derivatives. The AF adduct is known to exist in two distinct conformational motifs, depending upon the location of the hydrophobic fluorine moiety: major groove binding "B type" (B) conformation (AF-dGanti) and base-displaced "stacked" (S) conformation (AF-dGsyn). The AF-induced S/B conformational heterogeneity is sequence-dependent and follows a typical two-site dynamic chemical exchange. The population of S conformation decreases in the order of 3′-G > A ≫C > T, indicating the importance of the purine flanking bases in promoting the stacking structure. Line-shape analysis showed that the S/B interconversion energy barriers (ΔG ‡) are in the narrow 14-16 kcal/mol range. The energy differences of the two conformers are relatively small (<0.5 kcal/mol), suggesting a possibility for a facile adduct conformation switch in the active site of a polymerase. The S/B equilibrium modulates the efficiency of Escherichia coli UvrABC-based nucleotide excision repair (NER) in a conformation-specific manner. The 19F NMR/NER results indicate greater repair susceptibility for the base-displaced S conformer, which lacks a Watson - Crick base pair at the lesion site. These findings represent the first of its kind quantitative structure - function work relating NER activity to a specific adduct conformer and will lead to a better understanding of how bulky DNA adducts are accommodated by the repair protein. © 2007 American Chemical Society.
Chemical Research in Toxicology
Meneni, Srinivasa R., Steven M. Shell, Yue Zou, and Bongsup P. Cho. "Conformation-specific recognition of carcinogen-DNA adduct in Escherichia coli nucleotide excision repair." Chemical Research in Toxicology 20, 1 (2007): 6-10. doi:10.1021/tx600273h.