Evidence map›Paper›PMID 21345960›Full record

ArticleJournal of virology2011

Analysis of poliovirus protein 3A interactions with viral and cellular proteins in infected cells.

Natalya L Teterina, Yuval Pinto, Joseph D Weaver, Kenneth S Jensen, Ellie Ehrenfeld

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Manipulation of Host Cell Organelles by Intracellular Pathogens.International journal of molecular sciences · 2021
    Review
  5. Review
  6. Review
  7. Article
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  15. Article
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  17. Article
  18. Picornavirus--host interactions to construct viral secretory membranes.Progress in molecular biology and translational science · 2015
    Review
  19. Lipids and RNA virus replication.Current opinion in virology · 2014
    Review
  20. 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

5 authors at 2 institutions in 1 country.

Natalya L TeterinaLaboratory of Infections Diseases, National Institutes of Health, Bldg. 33, Room 3W10A.2, 33 North Drive, MSC 3203, Bethesda, MD 20892-3203, USA. nteterina@niaid.nih.gov
Yuval Pinto
Joseph D Weaver
Kenneth S Jensen
Ellie Ehrenfeld
National Institute of Allergy and Infectious Diseases · USNational Institutes of Health · US

Funding

Molecular Biology of Picornavirus ReplicationZIAAI000816 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI EHRENFELD, ELVERA · 2009 to 2010
$1.4M
Intramural NIH HHS
6 · The paper itself

Abstract

Poliovirus proteins 3A and 3AB are small, membrane-binding proteins that play multiple roles in viral RNA replication complex formation and function. In the infected cell, these proteins associate with other viral and cellular proteins as part of a supramolecular complex whose structure and composition are unknown. We isolated viable viruses with three different epitope tags (FLAG, hemagglutinin [HA], and c-myc) inserted into the N-terminal region of protein 3A. These viruses exhibited growth properties and characteristics very similar to those of the wild-type, untagged virus. Extracts prepared from the infected cells were subjected to immunoaffinity purification of the tagged proteins by adsorption to commercial antibody-linked beads and examined after elution for cellular and other viral proteins that remained bound to 3A sequences during purification. Viral proteins 2C, 2BC, 3D, and 3CD were detected in all three immunopurified 3A samples. Among the cellular proteins previously reported to interact with 3A either directly or indirectly, neither LIS1 nor phosphoinositol-4 kinase (PI4K) were detected in any of the purified tagged 3A samples. However, the guanine nucleotide exchange factor GBF1, which is a key regulator of membrane trafficking in the cellular protein secretory pathway and which has been shown previously to bind enteroviral protein 3A and to be required for viral RNA replication, was readily recovered along with immunoaffinity-purified 3A-FLAG. Surprisingly, we failed to cocapture GBF1 with 3A-HA or 3A-myc proteins. A model for variable binding of these 3A mutant proteins to GBF1 based on amino acid sequence motifs and the resulting practical and functional consequences thereof are discussed.

Indexed as

Host-Pathogen InteractionsProtein Interaction MappingHeLa CellsHumansMacromolecular SubstancesPoliovirusProtein BindingViral Core Proteins3A protein, PoliovirusMacromolecular SubstancesViral Core Proteins

Identifiers

PMID21345960
PMCPMC3126254
OpenAlexW2161218720

What OpenQuestion holds

Textmetadata
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.