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Effect of a U:G mispair on the water around DNA.
Mardt, Andreas; Gorriz, Rene F; Ferraro, Federica; Ulrich, Philip; Zahran, Mai; Imhof, Petra.
Afiliação
  • Mardt A; Department of Physics, Freie Universität Berlin, Arnimallee 14, 14195 Berlin, Germany.
  • Gorriz RF; Department of Physics, Freie Universität Berlin, Arnimallee 14, 14195 Berlin, Germany.
  • Ferraro F; Department for Chemistry and Pharmacy, Computer Chemistry Center, Friedrich-Alexander University (FAU) Erlangen Nürnberg, Nägelsbachstrasse 25, 91052 Erlangen, Germany.
  • Ulrich P; Department of Physics, Freie Universität Berlin, Arnimallee 14, 14195 Berlin, Germany.
  • Zahran M; New York City College of Technology, 718-260-5000 300 Jay St., Brooklyn, NY 11201, USA.
  • Imhof P; Department of Physics, Freie Universität Berlin, Arnimallee 14, 14195 Berlin, Germany; Department for Chemistry and Pharmacy, Computer Chemistry Center, Friedrich-Alexander University (FAU) Erlangen Nürnberg, Nägelsbachstrasse 25, 91052 Erlangen, Germany. Electronic address: petra.imhof@fau.de.
Biophys Chem ; 283: 106779, 2022 04.
Article em En | MEDLINE | ID: mdl-35217480
ABSTRACT
DNA repair proteins are able to discriminate DNA lesions among an abundance of intact DNA with high selectivity. To investigate detectable characteristics of one specific lesion, we compare statistical results from molecular dynamics simulations of two different DNA in water, one with an intact CG pair and one that contains a UG mispair, and perform a comparative analysis of the water dynamics around the two. Our data show that in addition to the local DNA conformation, also the surrounding water shell exhibits significant differences that may help mispair discrimination. The chemical groups which account for a UG mispair to exhibit a wobble conformation instead of the 'proper' Watson-Crick pairing of a CG pair, that is an oxygen atom (in uracil) instead of an amino group (in cytosine), also order the water molecules around the bases such that they act predominantly as hydrogen-bond donor or acceptor to the uracil or cytosine base, respectively. These changes in water conformation stretch into the second solvation shell, which may be exploited by repair enzymes to achieve lesion detection with high efficiency.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA / Água Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA / Água Idioma: En Ano de publicação: 2022 Tipo de documento: Article