On the absence of intrahelical DNA dynamics on the μs to ms timescale.

Nat Commun

Department of Medicinal Chemistry, L.S. Skaggs Pharmacy Institute, University of Utah, 2000 East 30 South Skaggs 307, Salt Lake City, Utah 84112, USA.

Published: October 2014

AI Article Synopsis

  • DNA helices exhibit motion across both short and long timescales, but significant movements in the 1 μs to 1 ms range are largely unobserved.
  • The lack of detectable motion in this intermediate timescale may help differentiate normal Watson-Crick base-paired DNA from damaged DNA.
  • This study utilizes advanced molecular dynamics simulations to explore long-timescale behaviors of a B-DNA duplex, aiming to support the hypothesis about static properties of specific DNA structures.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4215645PMC
http://dx.doi.org/10.1038/ncomms6152DOI Listing

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