Evidence map›Paper›PMID 28642595›Full record

ArticleScientific reports2017

3D Bayesian cluster analysis of super-resolution data reveals LAT recruitment to the T cell synapse.

Juliette Griffié, Leigh Shlomovich, David J Williamson, Michael Shannon, Jesse Aaron, Satya Khuon, Garth L Burn, Lies Boelen, Ruby Peters, Andrew P Cope and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
8.3field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
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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

13 authors at 4 institutions in 2 countries.

Juliette GriffiéDepartment of Physics and Randall Division of Cell and Molecular Biophysics, King's College London, London, UK. juliette.griffie@kcl.ac.uk.
Leigh ShlomovichDepartment of Mathematics, Imperial College London, London, UK.
David J WilliamsonDepartment of Physics and Randall Division of Cell and Molecular Biophysics, King's College London, London, UK.
Michael ShannonDepartment of Physics and Randall Division of Cell and Molecular Biophysics, King's College London, London, UK.
Jesse AaronAdvanced Imaging Center, Howard Hughes Medical Institute Janelia Research Campus, Ashburn, Virginia, USA.
Satya KhuonAdvanced Imaging Center, Howard Hughes Medical Institute Janelia Research Campus, Ashburn, Virginia, USA.
Garth L BurnDepartment of Physics and Randall Division of Cell and Molecular Biophysics, King's College London, London, UK.
Lies BoelenDepartment of Medicine, Imperial College London, London, UK.
Ruby PetersDepartment of Physics and Randall Division of Cell and Molecular Biophysics, King's College London, London, UK.
Andrew P CopeDepartment of Immunology, Infection and Inflammatory Disease, King's College London, London, UK.ORCID 0000-0003-0470-1827
Edward A K CohenDepartment of Mathematics, Imperial College London, London, UK.
Patrick Rubin-DelanchyDepartment of Statistics, University of Oxford, Oxford, UK.
Dylan M OwenDepartment of Physics and Randall Division of Cell and Molecular Biophysics, King's College London, London, UK.
King's College London · GBImperial College London · GBHoward Hughes Medical Institute · USUniversity of Oxford · GB

Funding

European Research Council 337187Versus Arthritis 20525
6 · The paper itself

Abstract

Single-molecule localisation microscopy (SMLM) allows the localisation of fluorophores with a precision of 10-30 nm, revealing the cell's nanoscale architecture at the molecular level. Recently, SMLM has been extended to 3D, providing a unique insight into cellular machinery. Although cluster analysis techniques have been developed for 2D SMLM data sets, few have been applied to 3D. This lack of quantification tools can be explained by the relative novelty of imaging techniques such as interferometric photo-activated localisation microscopy (iPALM). Also, existing methods that could be extended to 3D SMLM are usually subject to user defined analysis parameters, which remains a major drawback. Here, we present a new open source cluster analysis method for 3D SMLM data, free of user definable parameters, relying on a model-based Bayesian approach which takes full account of the individual localisation precisions in all three dimensions. The accuracy and reliability of the method is validated using simulated data sets. This tool is then deployed on novel experimental data as a proof of concept, illustrating the recruitment of LAT to the T-cell immunological synapse in data acquired by iPALM providing ~10 nm isotropic resolution.

Indexed as

Adaptor Proteins, Signal TransducingBayes TheoremCell LineCluster AnalysisHumansImmunological SynapsesLymphocyte ActivationMembrane ProteinsMicroscopyModels, BiologicalT-LymphocytesAdaptor Proteins, Signal TransducingLAT protein, humanMembrane Proteins

Identifiers

PMID28642595
PMCPMC5481387
OpenAlexW2625061534

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.