Evidence map›Paper›PMID 17227681›Full record

ArticleJournal of virological methods2007

Inactivation and purification of cowpea mosaic virus-like particles displaying peptide antigens from Bacillus anthracis.

Jamie P Phelps, Nghiep Dang, Lada Rasochova

Open access · greenAbstract read
In one paragraph

Article in Journal of virological methods, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 47 citations in OpenAlex.

  1. Biological Nanoparticles in Vaccine Development.Frontiers in bioengineering and biotechnology · 2022
    Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Virus-based nanoparticles as platform technologies for modern vaccines.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2016
    Review
  8. Review
  9. Review
  10. Review
  11. Applications of plant viruses in bionanotechnology.Current topics in microbiology and immunology · 2014
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Purification of Bionanoparticles.Chemical engineering & technology · 2008
    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 2 institutions in 1 country.

Jamie P PhelpsThe Dow Chemical Company, Dowpharma, San Diego, CA 92121, USA. PhelpsJ@colorado.edu <PhelpsJ@colorado.edu>
Nghiep Dang
Lada Rasochova
Dow Chemical (United States) · USPhelps Hospital · US

Funding

Non-Invasive Plant Virus Particle-Based Anthrax VaccinesU01AI054641 · NIAID · DOW CHEMICAL COMPANY · PI ANDERSON, WILLIAM KERR · 2003 to 2006
$5.7M
NIAID NIH HHS 1U01AI054641-01NIAID NIH HHS U01 AI054641NIAID NIH HHS U01 AI054641-03
6 · The paper itself

Abstract

Chimeric cowpea mosaic virus (CPMV) particles displaying foreign peptide antigens on the particle surface are suitable for development of peptide-based vaccines. However, commonly used PEG precipitation-based purification methods are not sufficient for production of high quality vaccine candidates because they do not allow for separation of chimeric particles from cleaved contaminating species. Moreover, the purified particles remain infectious to plants. To advance the CPMV technology further, it is necessary to develop efficient and scalable purification strategies and preferably eliminate the infectivity of chimeric viruses. CPMV was engineered to display a 25 amino acid peptide derived from the Bacillus anthracis protective antigen on the surface loop of the large coat protein subunit. The engineered virus was propagated in cowpea plants and assembled into chimeric virus particles displaying 60 copies of the peptide on the surface. An effective inactivation method was developed to produce non-infectious chimeric CPMV virus-like particles (VLPs). Uncleaved VLPs were separated from the contaminating cleaved forms by anion exchange chromatography. The yield of purified chimeric VLPs was 0.3 g kg(-1) of leaf tissue. The results demonstrate the ability to generate multi-gram quantities of non-infectious, chimeric CPMV VLPs in plants for use in the development of peptide-based vaccines.

Indexed as

Ammonium SulfateAntigens, BacterialBacillus anthracisBacterial ProteinsChromatography, Ion ExchangeComovirusFabaceaeHydrogen-Ion ConcentrationIndustrial MicrobiologyPlant LeavesReassortant VirusesRecombinant ProteinsVirus InactivationAmmonium SulfateAntigens, BacterialBacterial ProteinsRecombinant Proteins

Identifiers

PMID17227681
PMCPMC1952215
OpenAlexW2082687877

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.