Evidence map›Paper›PMID 24530430›Full record

ArticleJournal of virological methods2014

Cell adhesion as a novel approach to determining the cellular binding motif on the severe acute respiratory syndrome coronavirus spike protein.

Hsin-Hou Chang, Po-Kong Chen, Guan-Ling Lin, Chun-Jen Wang, Chih-Hsien Liao, Yu-Cheng Hsiao, Jing-Hua Dong, Der-Shan Sun

Abstract read
In one paragraph

Article in Journal of virological methods, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Reconstitution of the receptor-binding motif of the SARS coronavirus.Protein engineering, design & selection : PEDS · 2015
    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

8 authors.

Hsin-Hou ChangDepartment of Molecular Biology and Human Genetics, Tzu-Chi University, Hualien, Taiwan; Institute of Medical Sciences, Tzu-Chi University, Hualien, Taiwan.
Po-Kong ChenInstitute of Medical Sciences, Tzu-Chi University, Hualien, Taiwan.
Guan-Ling LinInstitute of Medical Sciences, Tzu-Chi University, Hualien, Taiwan.
Chun-Jen WangThe Department of Life Sciences, Tzu-Chi University, Hualien, Taiwan.
Chih-Hsien LiaoDepartment of Molecular Biology and Human Genetics, Tzu-Chi University, Hualien, Taiwan.
Yu-Cheng HsiaoDepartment of Molecular Biology and Human Genetics, Tzu-Chi University, Hualien, Taiwan.
Jing-Hua DongDepartment of Molecular Biology and Human Genetics, Tzu-Chi University, Hualien, Taiwan.
Der-Shan SunDepartment of Molecular Biology and Human Genetics, Tzu-Chi University, Hualien, Taiwan; Institute of Medical Sciences, Tzu-Chi University, Hualien, Taiwan. Electronic address: dssun@mail.tcu.edu.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging life threatening pathogens such as severe acute aspiratory syndrome-coronavirus (SARS-CoV), avian-origin influenzas H7N9, and the Middle East respiratory syndrome coronavirus (MERS-CoV) have caused a high case-fatality rate and psychological effects on society and the economy. Therefore, a simple, rapid, and safe method to investigate a therapeutic approach against these pathogens is required. In this study, a simple, quick, and safe cell adhesion inhibition assay was developed to determine the potential cellular binding site on the SARS-CoV spike protein. Various synthetic peptides covering the potential binding site helped to minimize further the binding motif to 10-25 residues. Following analyses, 2 peptides spanning the 436-445 and 437-461 amino acids of the spike protein were identified as peptide inhibitor or peptide vaccine candidates against SARS-CoV.

Indexed as

Cell AdhesionVirus AttachmentAnimalsAntiviral AgentsBinding SitesCell LineHumansPeptidesProtein BindingSevere acute respiratory syndrome-related coronavirusSpike Glycoprotein, CoronavirusAntiviral AgentsPeptidesSpike Glycoprotein, CoronavirusBinding motifSARS-CoVSpike proteinVero E6 cells

Identifiers

PMID24530430
PMCPMC7113645

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.