Evidence map›Paper›PMID 27038378›Full record

ReviewAdvances in protein chemistry and structural biology2016

Targeting the Channel Activity of Viroporins.

Janet To, Wahyu Surya, Jaume Torres

Open access · greenAbstract readReview
In one paragraph

Review in Advances in protein chemistry and structural biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
9.0field-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

22 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Membrane Condensation and Curvature Induced by SARS-CoV-2 Envelope Protein.Langmuir : the ACS journal of surfaces and colloids · 2024
    Article
  8. Viroporins of Mpox Virus.International journal of molecular sciences · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Spiers Memorial Lecture: Analysis andFaraday discussions · 2021
    Article
  15. Article
  16. Article
  17. Characterization of the SARS-CoV-2 E Protein: Sequence, Structure, Viroporin, and Inhibitors.Protein science : a publication of the Protein Society · 2021
    Review
  18. Article
  19. Article
  20. Review
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

3 authors at 1 institution in 1 country.

Janet ToSchool of Biological Sciences, Nanyang Technological University, Singapore.
Wahyu SuryaSchool of Biological Sciences, Nanyang Technological University, Singapore.
Jaume TorresSchool of Biological Sciences, Nanyang Technological University, Singapore. Electronic address: jtorres@ntu.edu.sg.
Nanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the discovery that certain small viral membrane proteins, collectively termed as viroporins, can permeabilize host cellular membranes and also behave as ion channels, attempts have been made to link this feature to specific biological roles. In parallel, most viroporins identified so far are virulence factors, and interest has focused toward the discovery of channel inhibitors that would have a therapeutic effect, or be used as research tools to understand the biological roles of viroporin ion channel activity. However, this paradigm is being shifted by the difficulties inherent to small viral membrane proteins, and by the realization that protein-protein interactions and other diverse roles in the virus life cycle may represent an equal, if not, more important target. Therefore, although targeting the channel activity of viroporins can probably be therapeutically useful in some cases, the focus may shift to their other functions in following years. Small-molecule inhibitors have been mostly developed against the influenza A M2 (IAV M2 or AM2). This is not surprising since AM2 is the best characterized viroporin to date, with a well-established biological role in viral pathogenesis combined the most extensive structural investigations conducted, and has emerged as a validated drug target. For other viroporins, these studies are still mostly in their infancy, and together with those for AM2, are the subject of the present review.

Indexed as

Protein Interaction MapsCell MembraneHumansIon ChannelsRetroviridae Proteins, OncogenicViral Envelope ProteinsViral Matrix ProteinsViral Nonstructural ProteinsViral ProteinsViral Regulatory and Accessory ProteinsViroporin Proteins2B protein, poliovirusagnoprotein, polyomavirusIon ChannelsM2 protein, Influenza A virusp7 protein, Hepatitis C virusRetroviridae Proteins, Oncogenicsmall hydrophobic protein, virusViral Envelope ProteinsViral Matrix ProteinsViral Nonstructural ProteinsViral ProteinsViral Regulatory and Accessory ProteinsViroporin ProteinsChannel activityDrug discoveryInhibitorsProtein–protein interactionsViroporinsViruses

Identifiers

PMID27038378
PMCPMC7102763
OpenAlexW2291889754

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.