Evidence map›Paper›PMID 15811330›Full record

ArticleFEBS letters2005

Synthetic peptides derived from SARS coronavirus S protein with diagnostic and therapeutic potential.

Wei Lu, Xiao-Dong Wu, Mu De Shi, Rui Fu Yang, You Yu He, Chao Bian, Tie Liu Shi, Sheng Yang, Xue-Liang Zhu, Wei-Hong Jiang and 12 more

Abstract read
In one paragraph

Article in FEBS letters, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. DCs-based therapies: potential strategies in severe SARS-CoV-2 infection.International journal of medical sciences · 2021
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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  17. 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

22 authors.

Wei LuLaboratory of Molecular Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Shanghai 200031, China.
Xiao-Dong Wu
Mu De Shi
Rui Fu Yang
You Yu He
Chao Bian
Tie Liu Shi
Sheng Yang
Xue-Liang Zhu
Wei-Hong Jiang
Yi Xue Li
Lin-Chen Yan
Yong Yong Ji
Ying Lin
Guo-Mei Lin
Lin Tian
Jin Wang
Hong Xia Wang
You Hua Xie
Gang Pei
Jia Rui Wu
Bing Sun

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spike (S) protein of severe acute respiratory syndrome coronavirus (SARS-CoV) is an important viral structural protein. Based on bioinformatics analysis, 10 antigenic peptides derived from the S protein sequence were selected and synthesized. The antigenicity and immunoreactivity of all the peptides were tested in vivo and in vitro. Four peptides (P6, P8, P9 and P10) which contain B cell epitopes of the S protein were identified, and P8 peptide was confirmed in vivo to have a potential in serological diagnosis. By using a syncytia formation model, we tested the neutralization ability of all 10 peptides and their corresponding antibodies. It is interesting to find that P8 and P9 peptides inhibited syncytia formation, suggesting that the P8 and P9 spanning regions may provide a good target for anti-SARS-CoV drug design. Our data suggest that we have identified peptides derived from the S protein of SARS-CoV, which are useful for SARS treatment and diagnosis.

Indexed as

Amino Acid SequenceBlotting, WesternComputational BiologyHumansMolecular Sequence DataPeptidesSevere acute respiratory syndrome-related coronavirusViral ProteinsPeptidesViral Proteins

Identifiers

PMID15811330
PMCPMC7094314

What OpenQuestion holds

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Registered trials

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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.