Evidence map›Paper›PMID 23429521›Full record

ArticleMolecular & cellular proteomics : MCP2013

Affinity capture and identification of host cell factors associated with hepatitis C virus (+) strand subgenomic RNA.

Alok Upadhyay, Updesh Dixit, Dinesh Manvar, Nootan Chaturvedi, Virendra N Pandey

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Effect of P-body component Mov10 on HCV virus production and infectivity.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Proteomics Tracing the Footsteps of Infectious Disease.Molecular & cellular proteomics : MCP · 2017
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Chaperones in hepatitis C virus infection.World journal of hepatology · 2016
    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.

Alok UpadhyayDepartment of Biochemistry and Molecular Biology and Centre for the Study of Emerging and Re-Emerging Pathogens, UMDNJ-New Jersey Medical School, Newark, New Jersey 07103, USA.
Updesh Dixit
Dinesh Manvar
Nootan Chaturvedi
Virendra N Pandey
Rutgers New Jersey Medical SchoolRutgers, The State University of New Jersey · US

Funding

Proteomics of HCV Replication ComplexR21AI073703 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI PANDEY, VIRENDRA NATH · 2009 to 2010
$429k
FUSE Binding Protein As a Cellular Effector of HCV ReplicationR21DK083560 · NIDDK · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI PANDEY, VIRENDRA NATH · 2010 to 2011
$427k
NIAID NIH HHS AI073703NIAID NIH HHS R21 AI073703NIDDK NIH HHS DK083560NIDDK NIH HHS R21 DK083560
6 · The paper itself

Abstract

Hepatitis C virus (HCV) infection leading to chronic hepatitis is a major factor in the causation of liver cirrhosis, hepatocellular carcinoma, and liver failure. This process may involve the interplay of various host cell factors, as well as the interaction of these factors with viral RNA and proteins. We report a novel strategy using a sequence-specific biotinylated peptide nucleic acid (PNA)-neamine conjugate targeted to HCV RNA for the in situ capture of subgenomic HCV (+) RNA, along with cellular and viral factors associated with it in MH14 host cells. Using this affinity capture system in conjunction with LC/MS/MS, we have identified 83 cellular factors and three viral proteins (NS5B, NS5A, and NS3-4a protease-helicase) associated with the viral genome. The capture was highly specific. These proteins were not scored with cured MH14 cells devoid of HCV replicons because of the absence of the target sequence in cells for the PNA-neamine probe and also because, unlike oligomeric DNA, cellular proteins have no affinity for PNA. The identified cellular factors belong to different functional groups, including signaling, oncogenic, chaperonin, transcriptional regulators, and RNA helicases as well as DEAD box proteins, ribosomal proteins, translational regulators/factors, and metabolic enzymes, that represent a diverse set of cellular factors associated with the HCV RNA genome. Small interfering RNA-mediated silencing of a diverse class of selected proteins in an HCV replicon cell line either enhanced or inhibited HCV replication/translation, suggesting that these cellular factors have regulatory roles in HCV replication.

Indexed as

Gene Expression Regulation, ViralGenome, ViralBiotinylationCell Line, TumorChromatography, AffinityChromatography, LiquidDEAD-box RNA HelicasesFramycetinHepacivirusHepatocytesHost-Pathogen InteractionsHumansNucleoside-TriphosphatasePeptide Nucleic AcidsProtein IsoformsRepliconDEAD-box RNA HelicasesFramycetinneamineNS3 protein, hepatitis C virusNS-5 protein, hepatitis C virusNucleoside-TriphosphatasePeptide Nucleic AcidsProtein IsoformsRNA-Dependent RNA PolymeraseRNA, ViralSerine EndopeptidasesViral Nonstructural ProteinsViral Proteases

Identifiers

PMID23429521
PMCPMC3675812
OpenAlexW2126789024

What Socratic 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 Socratic graph.