Evidence map›Paper›PMID 29858887›Full record

ArticleChemphyschem : a European journal of chemical physics and physical chemistry2018

Direct Prediction of EPR Spectra from Lipid Bilayers: Understanding Structure and Dynamics in Biological Membranes.

Andrea Catte, Gaye F White, Mark R Wilson, Vasily S Oganesyan

Open access · hybridAbstract read
In one paragraph

Article in Chemphyschem : a European journal of chemical physics and physical chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 35% of its field
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

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Unravelling Guest Dynamics in Crystalline Molecular Organics UsingJournal of the American Chemical Society · 2024
    Article
  2. Article
  3. Article
  4. Direct Prediction of EPR Spectra from Lipid Bilayers: Understanding Structure and Dynamics in Biological Membranes.Chemphyschem : a European journal of chemical physics and physical chemistry · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Andrea CatteSchool of Chemistry, University of East Anglia, Norwich, NR4 7TJ, UK.
Gaye F WhiteSchool of Chemistry, University of East Anglia, Norwich, NR4 7TJ, UK.
Mark R WilsonDepartment of Chemistry, Durham University, Lower Mountjoy, South Road, Durham, DH1 3 LE, UK.
Vasily S OganesyanSchool of Chemistry, University of East Anglia, Norwich, NR4 7TJ, UK.ORCID 0000-0002-8738-1146
University of East Anglia · GBDurham University · GB

Funding

EPSRC EP/L00111X/1EPSRC EP/L001322/1EPSRC EP/P007554/1Research and Specialist Computing Support service at the University of East AngliaUEA
6 · The paper itself

Abstract

Of the many biophysical techniques now being brought to bear on studies of membranes, electron paramagnetic resonance (EPR) of nitroxide spin probes was the first to provide information about both mobility and ordering in lipid membranes. Here, we report the first prediction of variable temperature EPR spectra of model lipid bilayers in the presence and absence of cholesterol from the results of large scale fully atomistic molecular dynamics (MD) simulations. Three types of structurally different spin probes were employed in order to study different parts of the bilayer. Our results demonstrate very good agreement with experiment and thus confirm the accuracy of the latest lipid force fields. The atomic resolution of the simulations allows the interpretation of the molecular motions and interactions in terms of their impact on the sensitive EPR line shapes. Direct versus indirect effects of cholesterol on the dynamics of spin probes are analysed. Given the complexity of structural organisation in lipid bilayers, the advantage of using a combined MD-EPR simulation approach is two-fold. Firstly, prediction of EPR line shapes directly from MD trajectories of actual phospholipid structures allows unambiguous interpretation of EPR spectra of biological membranes in terms of complex motions. Secondly, such an approach provides an ultimate test bed for the up-to-date MD simulation models employed in the studies of biological membranes, an area that currently attracts great attention.

Indexed as

Electron Spin Resonance Spectroscopy1,2-DipalmitoylphosphatidylcholineCholesterolLipid BilayersMolecular Dynamics SimulationNitric OxideSpin LabelsTemperature1,2-DipalmitoylphosphatidylcholineCholesterolLipid BilayersNitric OxideSpin Labelsbiological membranescholesterolEPR spectroscopymolecular dynamics simulationsspin probes

Identifiers

PMID29858887
PMCPMC6175124
OpenAlexW2806235608

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.