Despite the extensive data on dG-AAF, the major DNA adduct derived from the model carcinogen 2-acetylaminofluorene, little is known with respect to its solution structures. Here, we provide NMR/CD evidence for three conformers of dG-AAF in duplex DNA: major groove B-type (B), base-displaced stacked (S), and minor groove wedge (W). The S/B/W-conformational heterogeneities were found to be sensitive to the nature of the flanking DNA sequence contexts and pH. © 2010 American Chemical Society
The structure of an adduct between guanine and the carcinogen acetylaminofluorene has been examined ...
2-Acetylaminofluorene (AAF) is a prototype arylamine carcinogen that forms C8-substituted dG-AAF and...
We report novel induced circular dichroism (ICD) characteristics for probing the conformational hete...
19F NMR spectroscopy was used to probe the conformation of a DNA adduct derived from the carcinogen ...
A systematic spectroscopic and computational study was conducted in order to probe the influence of ...
A systematic spectroscopic and computational study was conducted in order to probe the influence of ...
Several chemical carcinogens form covalent adducts with cellular DNA. We have found that N-2-acetyl-...
In this paper, we have constructed double stranded helices (60-mers) containing a single N-2-acetyla...
We report a systematic and quantitative structure-function relationship study of the major N-[deoxyg...
Fluorescence spectroscopy was used to study carcinogen-induced conformational heterogeneity in DNA d...
Adduct-induced conformational heterogeneity complicates the understanding of how DNA adducts exert m...
We report a systematic and quantitative structure-function relationship study of the major N-[deoxyg...
Unusual DNA sequences are known to adopt interesting three-dimensional structures which might have i...
A new model is presented for acetylaminofluorene (AAF> modified Z-DNA, in which the carcinogen is...
2-Acetylaminofluorene (AAF) is a prototype aryl amine carcinogen that forms C8-substituted dG-AAF an...
The structure of an adduct between guanine and the carcinogen acetylaminofluorene has been examined ...
2-Acetylaminofluorene (AAF) is a prototype arylamine carcinogen that forms C8-substituted dG-AAF and...
We report novel induced circular dichroism (ICD) characteristics for probing the conformational hete...
19F NMR spectroscopy was used to probe the conformation of a DNA adduct derived from the carcinogen ...
A systematic spectroscopic and computational study was conducted in order to probe the influence of ...
A systematic spectroscopic and computational study was conducted in order to probe the influence of ...
Several chemical carcinogens form covalent adducts with cellular DNA. We have found that N-2-acetyl-...
In this paper, we have constructed double stranded helices (60-mers) containing a single N-2-acetyla...
We report a systematic and quantitative structure-function relationship study of the major N-[deoxyg...
Fluorescence spectroscopy was used to study carcinogen-induced conformational heterogeneity in DNA d...
Adduct-induced conformational heterogeneity complicates the understanding of how DNA adducts exert m...
We report a systematic and quantitative structure-function relationship study of the major N-[deoxyg...
Unusual DNA sequences are known to adopt interesting three-dimensional structures which might have i...
A new model is presented for acetylaminofluorene (AAF> modified Z-DNA, in which the carcinogen is...
2-Acetylaminofluorene (AAF) is a prototype aryl amine carcinogen that forms C8-substituted dG-AAF an...
The structure of an adduct between guanine and the carcinogen acetylaminofluorene has been examined ...
2-Acetylaminofluorene (AAF) is a prototype arylamine carcinogen that forms C8-substituted dG-AAF and...
We report novel induced circular dichroism (ICD) characteristics for probing the conformational hete...