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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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 |
work_keys_str_mv |
AT mahdibagherpoorhelabad baseflipindnastudiedbymoleculardynamicssimulationsofdifferentlyoxidizedformsofmethylcytosine AT nataliakanaan baseflipindnastudiedbymoleculardynamicssimulationsofdifferentlyoxidizedformsofmethylcytosine AT petraimhof baseflipindnastudiedbymoleculardynamicssimulationsofdifferentlyoxidizedformsofmethylcytosine |
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1725216932826710016 |