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On the absence of intra-helical DNA dynamics on the µs to ms timescale

DNA helices display a rich tapestry of motion on both short (< 100 ns) and long (> 1 ms) timescales. However, with the exception of mismatched or damaged DNA, experimental measures indicate that motions in the 1 µs to 1 ms range are effectively absent, which is often attributed to difficulties...

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Detalles Bibliográficos
Autores principales: Galindo-Murillo, Rodrigo, Roe, Daniel R., Cheatham, Thomas E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215645/
https://www.ncbi.nlm.nih.gov/pubmed/25351257
http://dx.doi.org/10.1038/ncomms6152
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author Galindo-Murillo, Rodrigo
Roe, Daniel R.
Cheatham, Thomas E.
author_facet Galindo-Murillo, Rodrigo
Roe, Daniel R.
Cheatham, Thomas E.
author_sort Galindo-Murillo, Rodrigo
collection PubMed
description DNA helices display a rich tapestry of motion on both short (< 100 ns) and long (> 1 ms) timescales. However, with the exception of mismatched or damaged DNA, experimental measures indicate that motions in the 1 µs to 1 ms range are effectively absent, which is often attributed to difficulties in measuring motions in this time range. We hypothesized that these motions have not been measured because there is effectively no motion on this timescale, as this provides a means to distinguish faithful Watson-Crick base paired DNA from damaged DNA. The absence of motion on this timescale would present a “static” DNA sequence-specific structure that matches the encounter timescales of proteins, thereby facilitating recognition. Here we report long timescale (~10-44 µs) molecular dynamics simulations of a B-DNA duplex structure that addresses this hypothesis using both an “Anton” machine and large ensembles of AMBER GPU simulations.
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spelling pubmed-42156452015-04-29 On the absence of intra-helical DNA dynamics on the µs to ms timescale Galindo-Murillo, Rodrigo Roe, Daniel R. Cheatham, Thomas E. Nat Commun Article DNA helices display a rich tapestry of motion on both short (< 100 ns) and long (> 1 ms) timescales. However, with the exception of mismatched or damaged DNA, experimental measures indicate that motions in the 1 µs to 1 ms range are effectively absent, which is often attributed to difficulties in measuring motions in this time range. We hypothesized that these motions have not been measured because there is effectively no motion on this timescale, as this provides a means to distinguish faithful Watson-Crick base paired DNA from damaged DNA. The absence of motion on this timescale would present a “static” DNA sequence-specific structure that matches the encounter timescales of proteins, thereby facilitating recognition. Here we report long timescale (~10-44 µs) molecular dynamics simulations of a B-DNA duplex structure that addresses this hypothesis using both an “Anton” machine and large ensembles of AMBER GPU simulations. 2014-10-29 /pmc/articles/PMC4215645/ /pubmed/25351257 http://dx.doi.org/10.1038/ncomms6152 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Galindo-Murillo, Rodrigo
Roe, Daniel R.
Cheatham, Thomas E.
On the absence of intra-helical DNA dynamics on the µs to ms timescale
title On the absence of intra-helical DNA dynamics on the µs to ms timescale
title_full On the absence of intra-helical DNA dynamics on the µs to ms timescale
title_fullStr On the absence of intra-helical DNA dynamics on the µs to ms timescale
title_full_unstemmed On the absence of intra-helical DNA dynamics on the µs to ms timescale
title_short On the absence of intra-helical DNA dynamics on the µs to ms timescale
title_sort on the absence of intra-helical dna dynamics on the µs to ms timescale
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215645/
https://www.ncbi.nlm.nih.gov/pubmed/25351257
http://dx.doi.org/10.1038/ncomms6152
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