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μABC: a systematic microsecond molecular dynamics study of tetranucleotide sequence effects in B-DNA

We present the results of microsecond molecular dynamics simulations carried out by the ABC group of laboratories on a set of B-DNA oligomers containing the 136 distinct tetranucleotide base sequences. We demonstrate that the resulting trajectories have extensively sampled the conformational space a...

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Autores principales: Pasi, Marco, Maddocks, John H., Beveridge, David, Bishop, Thomas C., Case, David A., Cheatham, Thomas, Dans, Pablo D., Jayaram, B., Lankas, Filip, Laughton, Charles, Mitchell, Jonathan, Osman, Roman, Orozco, Modesto, Pérez, Alberto, Petkevičiūtė, Daiva, Spackova, Nada, Sponer, Jiri, Zakrzewska, Krystyna, Lavery, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231739/
https://www.ncbi.nlm.nih.gov/pubmed/25260586
http://dx.doi.org/10.1093/nar/gku855
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author Pasi, Marco
Maddocks, John H.
Beveridge, David
Bishop, Thomas C.
Case, David A.
Cheatham, Thomas
Dans, Pablo D.
Jayaram, B.
Lankas, Filip
Laughton, Charles
Mitchell, Jonathan
Osman, Roman
Orozco, Modesto
Pérez, Alberto
Petkevičiūtė, Daiva
Spackova, Nada
Sponer, Jiri
Zakrzewska, Krystyna
Lavery, Richard
author_facet Pasi, Marco
Maddocks, John H.
Beveridge, David
Bishop, Thomas C.
Case, David A.
Cheatham, Thomas
Dans, Pablo D.
Jayaram, B.
Lankas, Filip
Laughton, Charles
Mitchell, Jonathan
Osman, Roman
Orozco, Modesto
Pérez, Alberto
Petkevičiūtė, Daiva
Spackova, Nada
Sponer, Jiri
Zakrzewska, Krystyna
Lavery, Richard
author_sort Pasi, Marco
collection PubMed
description We present the results of microsecond molecular dynamics simulations carried out by the ABC group of laboratories on a set of B-DNA oligomers containing the 136 distinct tetranucleotide base sequences. We demonstrate that the resulting trajectories have extensively sampled the conformational space accessible to B-DNA at room temperature. We confirm that base sequence effects depend strongly not only on the specific base pair step, but also on the specific base pairs that flank each step. Beyond sequence effects on average helical parameters and conformational fluctuations, we also identify tetranucleotide sequences that oscillate between several distinct conformational substates. By analyzing the conformation of the phosphodiester backbones, it is possible to understand for which sequences these substates will arise, and what impact they will have on specific helical parameters.
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spelling pubmed-42317392014-11-21 μABC: a systematic microsecond molecular dynamics study of tetranucleotide sequence effects in B-DNA Pasi, Marco Maddocks, John H. Beveridge, David Bishop, Thomas C. Case, David A. Cheatham, Thomas Dans, Pablo D. Jayaram, B. Lankas, Filip Laughton, Charles Mitchell, Jonathan Osman, Roman Orozco, Modesto Pérez, Alberto Petkevičiūtė, Daiva Spackova, Nada Sponer, Jiri Zakrzewska, Krystyna Lavery, Richard Nucleic Acids Res Structural Biology We present the results of microsecond molecular dynamics simulations carried out by the ABC group of laboratories on a set of B-DNA oligomers containing the 136 distinct tetranucleotide base sequences. We demonstrate that the resulting trajectories have extensively sampled the conformational space accessible to B-DNA at room temperature. We confirm that base sequence effects depend strongly not only on the specific base pair step, but also on the specific base pairs that flank each step. Beyond sequence effects on average helical parameters and conformational fluctuations, we also identify tetranucleotide sequences that oscillate between several distinct conformational substates. By analyzing the conformation of the phosphodiester backbones, it is possible to understand for which sequences these substates will arise, and what impact they will have on specific helical parameters. Oxford University Press 2014-10-29 2014-09-26 /pmc/articles/PMC4231739/ /pubmed/25260586 http://dx.doi.org/10.1093/nar/gku855 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Structural Biology
Pasi, Marco
Maddocks, John H.
Beveridge, David
Bishop, Thomas C.
Case, David A.
Cheatham, Thomas
Dans, Pablo D.
Jayaram, B.
Lankas, Filip
Laughton, Charles
Mitchell, Jonathan
Osman, Roman
Orozco, Modesto
Pérez, Alberto
Petkevičiūtė, Daiva
Spackova, Nada
Sponer, Jiri
Zakrzewska, Krystyna
Lavery, Richard
μABC: a systematic microsecond molecular dynamics study of tetranucleotide sequence effects in B-DNA
title μABC: a systematic microsecond molecular dynamics study of tetranucleotide sequence effects in B-DNA
title_full μABC: a systematic microsecond molecular dynamics study of tetranucleotide sequence effects in B-DNA
title_fullStr μABC: a systematic microsecond molecular dynamics study of tetranucleotide sequence effects in B-DNA
title_full_unstemmed μABC: a systematic microsecond molecular dynamics study of tetranucleotide sequence effects in B-DNA
title_short μABC: a systematic microsecond molecular dynamics study of tetranucleotide sequence effects in B-DNA
title_sort μabc: a systematic microsecond molecular dynamics study of tetranucleotide sequence effects in b-dna
topic Structural Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231739/
https://www.ncbi.nlm.nih.gov/pubmed/25260586
http://dx.doi.org/10.1093/nar/gku855
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