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Cytosine ribose flexibility in DNA: a combined NMR (13)C spin relaxation and molecular dynamics simulation study

Using (13)C spin relaxation NMR in combination with molecular dynamic (MD) simulations, we characterized internal motions within double-stranded DNA on the pico- to nano-second time scale. We found that the C–H vectors in all cytosine ribose moieties within the Dickerson–Drew dodecamer (5′-CGCGAATTC...

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Detalles Bibliográficos
Autores principales: Duchardt, Elke, Nilsson, Lennart, Schleucher, Jürgen
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2475628/
https://www.ncbi.nlm.nih.gov/pubmed/18579564
http://dx.doi.org/10.1093/nar/gkn375
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author Duchardt, Elke
Nilsson, Lennart
Schleucher, Jürgen
author_facet Duchardt, Elke
Nilsson, Lennart
Schleucher, Jürgen
author_sort Duchardt, Elke
collection PubMed
description Using (13)C spin relaxation NMR in combination with molecular dynamic (MD) simulations, we characterized internal motions within double-stranded DNA on the pico- to nano-second time scale. We found that the C–H vectors in all cytosine ribose moieties within the Dickerson–Drew dodecamer (5′-CGCGAATTCGCG-3′) are subject to high amplitude motions, while the other nucleotides are essentially rigid. MD simulations showed that repuckering is a likely motional model for the cytosine ribose moiety. Repuckering occurs with a time constant of around 100 ps. Knowledge of DNA dynamics will contribute to our understanding of the recognition specificity of DNA-binding proteins such as cytosine methyltransferase.
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spelling pubmed-24756282008-07-21 Cytosine ribose flexibility in DNA: a combined NMR (13)C spin relaxation and molecular dynamics simulation study Duchardt, Elke Nilsson, Lennart Schleucher, Jürgen Nucleic Acids Res RNA Using (13)C spin relaxation NMR in combination with molecular dynamic (MD) simulations, we characterized internal motions within double-stranded DNA on the pico- to nano-second time scale. We found that the C–H vectors in all cytosine ribose moieties within the Dickerson–Drew dodecamer (5′-CGCGAATTCGCG-3′) are subject to high amplitude motions, while the other nucleotides are essentially rigid. MD simulations showed that repuckering is a likely motional model for the cytosine ribose moiety. Repuckering occurs with a time constant of around 100 ps. Knowledge of DNA dynamics will contribute to our understanding of the recognition specificity of DNA-binding proteins such as cytosine methyltransferase. Oxford University Press 2008-07 2008-06-25 /pmc/articles/PMC2475628/ /pubmed/18579564 http://dx.doi.org/10.1093/nar/gkn375 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle RNA
Duchardt, Elke
Nilsson, Lennart
Schleucher, Jürgen
Cytosine ribose flexibility in DNA: a combined NMR (13)C spin relaxation and molecular dynamics simulation study
title Cytosine ribose flexibility in DNA: a combined NMR (13)C spin relaxation and molecular dynamics simulation study
title_full Cytosine ribose flexibility in DNA: a combined NMR (13)C spin relaxation and molecular dynamics simulation study
title_fullStr Cytosine ribose flexibility in DNA: a combined NMR (13)C spin relaxation and molecular dynamics simulation study
title_full_unstemmed Cytosine ribose flexibility in DNA: a combined NMR (13)C spin relaxation and molecular dynamics simulation study
title_short Cytosine ribose flexibility in DNA: a combined NMR (13)C spin relaxation and molecular dynamics simulation study
title_sort cytosine ribose flexibility in dna: a combined nmr (13)c spin relaxation and molecular dynamics simulation study
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2475628/
https://www.ncbi.nlm.nih.gov/pubmed/18579564
http://dx.doi.org/10.1093/nar/gkn375
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