Evidence map›Paper›PMID 33907198›Full record

ArticleScientific reports2021

An efficient alpha helix model and simulation framework for stationary electrostatic interaction force estimation.

Guy G Butcher, William S Harwin, Chris I Jones

Abstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Guy G ButcherSchool of Biological Sciences, University of Reading, Reading, England. guy.butcher@pgr.reading.ac.uk.
William S HarwinSchool of Biological Sciences, University of Reading, Reading, England.
Chris I JonesSchool of Biological Sciences, University of Reading, Reading, England.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The alpha-helix coiled-coils within talin's rod domain have mechanical and signalling functions through their unfolding and refolding dynamics. A better understanding of talin unfolding events and the forces that are involved should allow better prediction of talin signalling. To overcome the current limitations of force measuring in molecular dynamics simulations, a new simulation framework was developed which operated directly within the force domain. Along with a corresponding alpha-helix modelling method, the simulation framework was developed drawing on robotic kinematics to specifically target force interactions. Coordinate frames were used efficiently to compartmentalise the simulation structures and static analysis was applied to determine the propagation of forces and torques through the protein structure. The results of the electrostatic approximation using Coulomb's law shows a simulated force interaction within the physiological relevant range of 5-40 pN for the rod sub-domains of talin. This covers the range of forces talin operates in and is 2-3 orders of magnitude closer to experimentally measured values than the compared all-atom and coarse-grained molecular dynamics. This targeted, force-based simulation is, therefore, able to produce more realistic forces values than previous simulation methods.

Identifiers

PMID33907198
PMCPMC8079384

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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.