Base Flip in DNA Studied by Molecular Dynamics Simulationsof Differently-Oxidized Forms of Methyl-Cytosine

Distortions in the DNA sequence, such as damage or mispairs, are specifically recognized and processed by DNA repair enzymes. Many repair proteins and, in particular, glycosylases flip the target base out of the DNA helix into the enzyme’s active site. Our molecular dynamics simulations of DNA with...

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Main Authors: Mahdi Bagherpoor Helabad, Natalia Kanaan, Petra Imhof
Format: Article
Language:English
Published: MDPI AG 2014-07-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/15/7/11799
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spelling doaj-02c8a04f09e444a1a4c54eb56eec4b512020-11-25T00:59:40ZengMDPI AGInternational Journal of Molecular Sciences1422-00672014-07-01157117991181610.3390/ijms150711799ijms150711799Base Flip in DNA Studied by Molecular Dynamics Simulationsof Differently-Oxidized Forms of Methyl-CytosineMahdi Bagherpoor Helabad0Natalia Kanaan1Petra Imhof2Institute of Theoretical Physics, Free University Berlin, Arnimallee 14, 14195 Berlin, GermanyInstitute of Theoretical Physics, Free University Berlin, Arnimallee 14, 14195 Berlin, GermanyInstitute of Theoretical Physics, Free University Berlin, Arnimallee 14, 14195 Berlin, GermanyDistortions in the DNA sequence, such as damage or mispairs, are specifically recognized and processed by DNA repair enzymes. Many repair proteins and, in particular, glycosylases flip the target base out of the DNA helix into the enzyme’s active site. Our molecular dynamics simulations of DNA with intact and damaged (oxidized) methyl-cytosine show that the probability of being flipped is similar for damaged and intact methyl-cytosine. However, the accessibility of the different 5-methyl groups allows direct discrimination of the oxidized forms. Hydrogen-bonded patterns that vary between methyl-cytosine forms carrying a carbonyl oxygen atom are likely to be detected by the repair enzymes and may thus help target site recognition.http://www.mdpi.com/1422-0067/15/7/11799DNA damagebase flipmolecular dynamics simulationsDNA recognition
collection DOAJ
language English
format Article
sources DOAJ
author Mahdi Bagherpoor Helabad
Natalia Kanaan
Petra Imhof
spellingShingle Mahdi Bagherpoor Helabad
Natalia Kanaan
Petra Imhof
Base Flip in DNA Studied by Molecular Dynamics Simulationsof Differently-Oxidized Forms of Methyl-Cytosine
International Journal of Molecular Sciences
DNA damage
base flip
molecular dynamics simulations
DNA recognition
author_facet Mahdi Bagherpoor Helabad
Natalia Kanaan
Petra Imhof
author_sort Mahdi Bagherpoor Helabad
title Base Flip in DNA Studied by Molecular Dynamics Simulationsof Differently-Oxidized Forms of Methyl-Cytosine
title_short Base Flip in DNA Studied by Molecular Dynamics Simulationsof Differently-Oxidized Forms of Methyl-Cytosine
title_full Base Flip in DNA Studied by Molecular Dynamics Simulationsof Differently-Oxidized Forms of Methyl-Cytosine
title_fullStr Base Flip in DNA Studied by Molecular Dynamics Simulationsof Differently-Oxidized Forms of Methyl-Cytosine
title_full_unstemmed Base Flip in DNA Studied by Molecular Dynamics Simulationsof Differently-Oxidized Forms of Methyl-Cytosine
title_sort base flip in dna studied by molecular dynamics simulationsof differently-oxidized forms of methyl-cytosine
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2014-07-01
description Distortions in the DNA sequence, such as damage or mispairs, are specifically recognized and processed by DNA repair enzymes. Many repair proteins and, in particular, glycosylases flip the target base out of the DNA helix into the enzyme’s active site. Our molecular dynamics simulations of DNA with intact and damaged (oxidized) methyl-cytosine show that the probability of being flipped is similar for damaged and intact methyl-cytosine. However, the accessibility of the different 5-methyl groups allows direct discrimination of the oxidized forms. Hydrogen-bonded patterns that vary between methyl-cytosine forms carrying a carbonyl oxygen atom are likely to be detected by the repair enzymes and may thus help target site recognition.
topic DNA damage
base flip
molecular dynamics simulations
DNA recognition
url http://www.mdpi.com/1422-0067/15/7/11799
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AT nataliakanaan baseflipindnastudiedbymoleculardynamicssimulationsofdifferentlyoxidizedformsofmethylcytosine
AT petraimhof baseflipindnastudiedbymoleculardynamicssimulationsofdifferentlyoxidizedformsofmethylcytosine
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