Evidence map›Paper›PMID 33239640›Full record

ArticleNature communications2020

Spatial proteomics defines the content of trafficking vesicles captured by golgin tethers.

John J H Shin, Oliver M Crook, Alicia C Borgeaud, Jérôme Cattin-Ortolá, Sew Y Peak-Chew, Lisa M Breckels, Alison K Gillingham, Jessica Chadwick, Kathryn S Lilley, Sean Munro

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.1field-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

55 citing papers in PubMed, 85 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

John J H ShinMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, CB2 0QH, UK. shin.jaehee@gmail.com.ORCID 0000-0002-8905-8350
Oliver M CrookThe Milner Therapeutics Institute, University of Cambridge, Cambridge, CB2 0AW, UK.ORCID 0000-0001-5669-8506
Alicia C BorgeaudMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, CB2 0QH, UK.ORCID 0000-0002-7231-7424
Jérôme Cattin-OrtoláMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, CB2 0QH, UK.ORCID 0000-0002-8988-4265
Sew Y Peak-ChewMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, CB2 0QH, UK.ORCID 0000-0002-7602-6384
Lisa M BreckelsCambridge Centre for Proteomics, Department of Biochemistry, University of Cambridge, Cambridge, CB2 1QR, UK.ORCID 0000-0001-8918-7171
Alison K GillinghamMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, CB2 0QH, UK.
Jessica ChadwickMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, CB2 0QH, UK.
Kathryn S LilleyThe Milner Therapeutics Institute, University of Cambridge, Cambridge, CB2 0AW, UK.
Sean MunroMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, CB2 0QH, UK. sean@mrc-lmb.cam.ac.uk.ORCID 0000-0001-6160-5773
MRC Laboratory of Molecular Biology · GBUniversity of Cambridge · GB

Funding

Medical Research Council MC_U105178783Wellcome Trust
6 · The paper itself

Abstract

Intracellular traffic between compartments of the secretory and endocytic pathways is mediated by vesicle-based carriers. The proteomes of carriers destined for many organelles are ill-defined because the vesicular intermediates are transient, low-abundance and difficult to purify. Here, we combine vesicle relocalisation with organelle proteomics and Bayesian analysis to define the content of different endosome-derived vesicles destined for the trans-Golgi network (TGN). The golgin coiled-coil proteins golgin-97 and GCC88, shown previously to capture endosome-derived vesicles at the TGN, were individually relocalised to mitochondria and the content of the subsequently re-routed vesicles was determined by organelle proteomics. Our findings reveal 45 integral and 51 peripheral membrane proteins re-routed by golgin-97, evidence for a distinct class of vesicles shared by golgin-97 and GCC88, and various cargoes specific to individual golgins. These results illustrate a general strategy for analysing intracellular sub-proteomes by combining acute cellular re-wiring with high-resolution spatial proteomics.

Indexed as

AutoantigensEndosomesGene Knockdown TechniquesGolgi Matrix ProteinsHEK293 CellsHeLa CellsHumansMembrane ProteinsMitochondriaProteomicsSpatial Analysistrans-Golgi NetworkAutoantigensGCC1 protein, humanGOLGA4 protein, humanGolgi complex autoantigen, 97-kDaGolgi Matrix ProteinsMembrane Proteins

Identifiers

PMID33239640
PMCPMC7689464
OpenAlexW3110060414

What OpenQuestion holds

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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.