Evidence map›Paper›PMID 32092106›Full record

ArticlePloS one2020

Preparation and purification of mono-ubiquitinated proteins using Avi-tagged ubiquitin.

Winnie Tan, Vincent J Murphy, Aude Charron, Sylvie van Twest, Michael Sharp, Angelos Constantinou, Michael W Parker, Wayne Crismani, Rohan Bythell-Douglas, Andrew J Deans

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. A RareGenes · 2022
    Article
  8. Site-specific ubiquitination: Deconstructing the degradation tag.Current opinion in structural biology · 2022
    Review
  9. Review
  10. Tools for Decoding Ubiquitin Signaling in DNA Repair.Frontiers in cell and developmental biology · 2021
    Review
  11. Article
  12. Article
  13. 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

10 authors at 4 institutions in 2 countries.

Winnie TanGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.ORCID 0000-0003-3229-4157
Vincent J MurphyGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.
Aude CharronGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.ORCID 0000-0002-8196-6047
Sylvie van TwestGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.
Michael SharpGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.ORCID 0000-0002-1019-3729
Angelos ConstantinouInstitute of Human Genetics (IGH), Centre National de la Recherche Scientifique (CNRS), Université de Montpellier (UM), Montpellier, France.
Michael W ParkerStructural Biology Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.ORCID 0000-0002-3101-1138
Wayne CrismaniGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.ORCID 0000-0003-0143-8293
Rohan Bythell-DouglasGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.
Andrew J DeansGenome Stability Unit, St. Vincent's Institute of Medical Research, Fitzroy, Victoria, Australia.ORCID 0000-0002-5271-4422
The University of Melbourne · AUSt Vincents Institute of Medical Research · AUCentre National de la Recherche Scientifique · FRÉcole Nationale Supérieure de Chimie de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Site-specific conjugation of ubiquitin onto a range of DNA repair proteins regulates their critical functions in the DNA damage response. Biochemical and structural characterization of these functions are limited by an absence of tools for the purification of DNA repair proteins in purely the ubiquitinated form. To overcome this barrier, we designed a ubiquitin fusion protein that is N-terminally biotinylated and can be conjugated by E3 RING ligases onto various substrates. Biotin affinity purification of modified proteins, followed by cleavage of the affinity tag leads to release of natively-mono-ubiquitinated substrates. As proof-of-principle, we applied this method to several substrates of mono-ubiquitination in the Fanconi anemia (FA)-BRCA pathway of DNA interstrand crosslink repair. These include the FANCI:FANCD2 complex, the PCNA trimer and BRCA1 modified nucleosomes. This method provides a simple approach to study the role of mono-ubiquitination in DNA repair or any other mono-ubiquitination signaling pathways.

Indexed as

Fanconi Anemia Complementation Group D2 ProteinFanconi Anemia Complementation Group ProteinsProliferating Cell Nuclear AntigenUbiquitinUbiquitin-Protein LigasesAnimalsAvidinHumansSf9 CellsSpodopteraUbiquitinated ProteinsAvidinBRAP protein, humanFANCD2 protein, humanFANCI protein, humanFanconi Anemia Complementation Group D2 ProteinFanconi Anemia Complementation Group ProteinsPCNA protein, humanProliferating Cell Nuclear AntigenUbiquitinUbiquitinated ProteinsUbiquitin-Protein Ligases

Identifiers

PMID32092106
PMCPMC7039436
OpenAlexW3007732400

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.