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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...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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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. |
format | Online Article Text |
id | pubmed-4231739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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