Evidence map›Paper›PMID 27681439›Full record

ArticleCell reports2016

DEEPN as an Approach for Batch Processing of Yeast 2-Hybrid Interactions.

Natasha Pashkova, Tabitha A Peterson, Venkatramanan Krishnamani, Patrick Breheny, Mark Stamnes, Robert C Piper

Abstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Powdery mildew effectors AVRMolecular plant pathology · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Newer Methods Drive Recent Insights into Rab GTPase Biology: An Overview.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  11. Article
  12. Informatic Analysis of Sequence Data from Batch Yeast 2-Hybrid Screens.Journal of visualized experiments : JoVE · 2018
    Article
  13. A Yeast 2-Hybrid Screen in Batch to Compare Protein Interactions.Journal of visualized experiments : JoVE · 2018
    Article
  14. 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

6 authors.

Natasha PashkovaDepartment of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA 52242, USA.
Tabitha A PetersonDepartment of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA 52242, USA.
Venkatramanan KrishnamaniDepartment of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA 52242, USA.
Patrick BrehenyDepartment of Biostatistics, University of Iowa, Iowa City, IA 52242, USA.
Mark StamnesDepartment of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA 52242, USA.
Robert C PiperDepartment of Molecular Physiology and Biophysics, University of Iowa, Iowa City, IA 52242, USA. Electronic address: robert-piper@uiowa.edu.

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
INTERDISCIPLINARY CARDIOVASCULAR RESEARCH FELLOWSHIPT32HL007121 · NHLBI · UNIVERSITY OF IOWA · PI LONDON, BARRY · 1985 to 2020
$15.1M
Ubiquitin-Dependent Sorting in Endosomes and the TGNR01GM058202 · NIGMS · UNIVERSITY OF IOWA · PI PIPER, ROBERT C · 1998 to 2025
$8.9M
NHLBI NIH HHS T32 HL007121NIGMS NIH HHS R01 GM058202
6 · The paper itself

Abstract

We adapted the yeast 2-hybrid assay to simultaneously uncover multiple transient protein interactions within a single screen by using a strategy termed DEEPN (dynamic enrichment for evaluation of protein networks). This approach incorporates high-throughput DNA sequencing and computation to follow competition among a plasmid population encoding interacting partners. To demonstrate the capacity of DEEPN, we identify a wide range of ubiquitin-binding proteins, including interactors that we verify biochemically. To demonstrate the specificity of DEEPN, we show that DEEPN allows simultaneous comparison of candidate interactors across multiple bait proteins, allowing differential interactions to be identified. This feature was used to identify interactors that distinguish between GTP- and GDP-bound conformations of Rab5.

Indexed as

Gene ExpressionHigh-Throughput Nucleotide SequencingPlasmidsProtein BindingProtein Interaction Mappingrab5 GTP-Binding ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSoftwareTwo-Hybrid System TechniquesUbiquitinrab5 GTP-Binding ProteinsSaccharomyces cerevisiae ProteinsUbiquitinprotein interactionsprotein networksubiquitin

Identifiers

PMID27681439
PMCPMC5594928

What OpenQuestion holds

Textmetadata
LicenceTDM
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.