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Structural basis for the selective incorporation of an artificial nucleotide opposite a DNA adduct by a DNA polymerase

Structural basis for the selective incorporation of an artificial nucleotide opposite a DNA adduct by a DNA polymerase

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BETZ, Karin, Arman NILFOROUSHAN, Laura A. WYSS, Kay DIEDERICHS, Shana J. STURLA, Andreas MARX, 2017. Structural basis for the selective incorporation of an artificial nucleotide opposite a DNA adduct by a DNA polymerase. In: Chemical Communications : ChemComm. 53(94), pp. 12704-12707. ISSN 1359-7345. eISSN 1364-548X. Available under: doi: 10.1039/c7cc07173f

@article{Betz2017-11-23Struc-40878, title={Structural basis for the selective incorporation of an artificial nucleotide opposite a DNA adduct by a DNA polymerase}, year={2017}, doi={10.1039/c7cc07173f}, number={94}, volume={53}, issn={1359-7345}, journal={Chemical Communications : ChemComm}, pages={12704--12707}, author={Betz, Karin and Nilforoushan, Arman and Wyss, Laura A. and Diederichs, Kay and Sturla, Shana J. and Marx, Andreas} }

Wyss, Laura A. 2017-12-08T13:20:12Z Betz, Karin Marx, Andreas Betz, Karin 2017-12-08T13:20:12Z Sturla, Shana J. Diederichs, Kay Structural basis for the selective incorporation of an artificial nucleotide opposite a DNA adduct by a DNA polymerase Nilforoushan, Arman Marx, Andreas terms-of-use Sturla, Shana J. Wyss, Laura A. Nilforoushan, Arman 2017-11-23 The possibility to sequence cytotoxic O<sup>6</sup>-alkylG DNA adducts would greatly benefit research. Recently we reported a benzimidazole-derived nucleotide that is selectively incorporated opposite the damaged site by a mutated DNA polymerase. Here we provide the structural basis for this reaction which may spur future developments in DNA damage sequencing. Diederichs, Kay eng

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