Evidence map›Paper›PMID 28288277›Full record

ArticleJournal of chemical theory and computation2017

Direct Comparison of Amino Acid and Salt Interactions with Double-Stranded and Single-Stranded DNA from Explicit-Solvent Molecular Dynamics Simulations.

Casey T Andrews, Brady A Campbell, Adrian H Elcock

Erratum issuedAbstract readComparative Study
In one paragraph

Article in Journal of chemical theory and computation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Frameshifting preserves key physicochemical properties of proteins.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Casey T AndrewsDepartment of Biochemistry, University of Iowa , Iowa City, Iowa 52242, United States.
Brady A CampbellDepartment of Biochemistry, University of Iowa , Iowa City, Iowa 52242, United States.
Adrian H ElcockDepartment of Biochemistry, University of Iowa , Iowa City, Iowa 52242, United States.ORCID http://orcid.org/0000-0003-2820-1376

Funding

Molecular Simulations of Folding & Association in Physiological EnvironmentsR01GM087290 · NIGMS · UNIVERSITY OF IOWA · PI ELCOCK, ADRIAN HAMILTON · 2009 to 2017
$1.6M
Molecular Simulations of Cotranslational FoldingR01GM099865 · NIGMS · UNIVERSITY OF IOWA · PI ELCOCK, ADRIAN HAMILTON · 2012 to 2015
$1.0M
NIGMS NIH HHS R01 GM087290NIGMS NIH HHS R01 GM099865
6 · The paper itself

Abstract

Given the ubiquitous nature of protein-DNA interactions, it is important to understand the interaction thermodynamics of individual amino acid side chains for DNA. One way to assess these preferences is to perform molecular dynamics (MD) simulations. Here we report MD simulations of 20 amino acid side chain analogs interacting simultaneously with both a 70-base-pair double-stranded DNA and with a 70-nucleotide single-stranded DNA. The relative preferences of the amino acid side chains for dsDNA and ssDNA match well with values deduced from crystallographic analyses of protein-DNA complexes. The estimated apparent free energies of interaction for ssDNA, on the other hand, correlate well with previous simulation values reported for interactions with isolated nucleobases, and with experimental values reported for interactions with guanosine. Comparisons of the interactions with dsDNA and ssDNA indicate that, with the exception of the positively charged side chains, all types of amino acid side chain interact more favorably with ssDNA, with intercalation of aromatic and aliphatic side chains being especially notable. Analysis of the data on a base-by-base basis indicates that positively charged side chains, as well as sodium ions, preferentially bind to cytosine in ssDNA, and that negatively charged side chains, and chloride ions, preferentially bind to guanine in ssDNA. These latter observations provide a novel explanation for the lower salt dependence of DNA duplex stability in GC-rich sequences relative to AT-rich sequences.

Indexed as

Molecular Dynamics SimulationAmino AcidsDNASaltsSolventsThermodynamicsAmino AcidsDNASaltsSolvents

Identifiers

PMID28288277
PMCPMC5543776

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.