Evidence map›Paper›PMID 33255849›Full record

ArticleMolecules (Basel, Switzerland)2020

In Silico Discovery of Antimicrobial Peptides as an Alternative to Control SARS-CoV-2.

Yamil Liscano, Jose Oñate-Garzón, Iván Darío Ocampo-Ibáñez

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Mechanisms and regulation of defensins in host defense.Signal transduction and targeted therapy · 2023
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. New Advances in Short Peptides: Looking Forward.Molecules (Basel, Switzerland) · 2022
    Article
  12. Review
  13. Advances in Research of Short Peptides.Molecules (Basel, Switzerland) · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Antimicrobial Peptides: A Potent Alternative to Antibiotics.Antibiotics (Basel, Switzerland) · 2021
    Review
  19. 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

3 authors at 1 institution in 1 country.

Yamil LiscanoResearch Group of Chemical and Biotechnology, Faculty of Basic Sciences, Universidad Santiago de Cali, Cali 760035, Colombia.ORCID 0000-0002-2674-8725
Jose Oñate-GarzónResearch Group of Chemical and Biotechnology, Faculty of Basic Sciences, Universidad Santiago de Cali, Cali 760035, Colombia.ORCID 0000-0002-9069-8902
Iván Darío Ocampo-IbáñezResearch Group of Microbiology, Industry and Environment, Faculty of Basic Sciences, Universidad Santiago de Cali, Cali 760035, Colombia.ORCID 0000-0002-9833-3537
Universidad Santiago de Cali · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A serious pandemic has been caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The interaction between spike surface viral protein (Sgp) and the angiotensin-converting enzyme 2 (ACE2) cellular receptor is essential to understand the SARS-CoV-2 infectivity and pathogenicity. Currently, no drugs are available to treat the infection caused by this coronavirus and the use of antimicrobial peptides (AMPs) may be a promising alternative therapeutic strategy to control SARS-CoV-2. In this study, we investigated the in silico interaction of AMPs with viral structural proteins and host cell receptors. We screened the antimicrobial peptide database (APD3) and selected 15 peptides based on their physicochemical and antiviral properties. The interactions of AMPs with Sgp and ACE2 were performed by docking analysis. The results revealed that two amphibian AMPs, caerin 1.6 and caerin 1.10, had the highest affinity for Sgp proteins while interaction with the ACE2 receptor was reduced. The effective AMPs interacted particularly with Arg995 located in the S2 subunits of Sgp, which is key subunit that plays an essential role in viral fusion and entry into the host cell through ACE2. Given these computational findings, new potentially effective AMPs with antiviral properties for SARS-CoV-2 were identified, but they need experimental validation for their therapeutic effectiveness.

Indexed as

COVID-19 Drug TreatmentAmphibian ProteinsAngiotensin-Converting Enzyme 2Antimicrobial Cationic PeptidesAntiviral AgentsBinding SitesComputer SimulationCOVID-19HumansPandemicsPore Forming Cytotoxic ProteinsProtein BindingSARS-CoV-2Spike Glycoprotein, CoronavirusViral Structural ProteinsAmphibian ProteinsAngiotensin-Converting Enzyme 2Antimicrobial Cationic PeptidesAntiviral Agentscaerin 1.6 protein, LitoriaPore Forming Cytotoxic ProteinsSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Viral Structural Proteinsangiotensin-converting enzyme 2antimicrobial peptidesSARS-CoV-2spike protein

Identifiers

PMID33255849
PMCPMC7728342
OpenAlexW3109039151

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.