Evidence map›Paper›PMID 36216816›Full record

ArticleNature communications2022

Inferring differential subcellular localisation in comparative spatial proteomics using BANDLE.

Oliver M Crook, Colin T R Davies, Lisa M Breckels, Josie A Christopher, Laurent Gatto, Paul D W Kirk, Kathryn S Lilley

Abstract read
In one paragraph

Article in Nature communications, 2022. 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
–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

17 citing papers in PubMed.

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  17. Subcellular proteomics.Nature reviews. Methods primers · 2021
    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

7 authors.

Oliver M CrookCambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge, CB2 1GA, Cambridge, UK. oliver.crook@stats.ox.ac.uk.ORCID 0000-0001-5669-8506
Colin T R DaviesCambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge, CB2 1GA, Cambridge, UK.ORCID 0000-0002-3156-543X
Lisa M BreckelsCambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge, CB2 1GA, Cambridge, UK.ORCID 0000-0001-8918-7171
Josie A ChristopherCambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge, CB2 1GA, Cambridge, UK.ORCID 0000-0001-7077-4894
Laurent Gattode Duve Institute, Université catholique de Louvain, Avenue Hippocrate 75, 1200, Brussels, Belgium.ORCID 0000-0002-1520-2268
Paul D W KirkMRC Biostatistics Unit, School of Clinical Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0002-5931-7489
Kathryn S LilleyCambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge, CB2 1GA, Cambridge, UK. k.s.lilley@bioc.cam.ac.uk.ORCID 0000-0003-0594-6543

Funding

Department of HealthMedical Research Council MC_UU_00002/13Wellcome Trust 110071/Z/15/ZWellcome Trust 110170/Z/15/Z
6 · The paper itself

Abstract

The steady-state localisation of proteins provides vital insight into their function. These localisations are context specific with proteins translocating between different subcellular niches upon perturbation of the subcellular environment. Differential localisation, that is a change in the steady-state subcellular location of a protein, provides a step towards mechanistic insight of subcellular protein dynamics. High-accuracy high-throughput mass spectrometry-based methods now exist to map the steady-state localisation and re-localisation of proteins. Here, we describe a principled Bayesian approach, BANDLE, that uses these data to compute the probability that a protein differentially localises upon cellular perturbation. Extensive simulation studies demonstrate that BANDLE reduces the number of both type I and type II errors compared to existing approaches. Application of BANDLE to several datasets recovers well-studied translocations. In an application to cytomegalovirus infection, we obtain insights into the rewiring of the host proteome. Integration of other high-throughput datasets allows us to provide the functional context of these data.

Indexed as

ProteomeProteomicsBayes TheoremMass SpectrometrySubcellular FractionsProteome

Identifiers

PMID36216816
PMCPMC9550814

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.