Evidence map›Paper›PMID 21390296›Full record

ArticlePloS one2011

Synthetic protocells interact with viral nanomachinery and inactivate pathogenic human virus.

Matteo Porotto, Feng Yi, Anne Moscona, David A LaVan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Ligand-targeted theranostic nanomedicines against cancer.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Biomimetic delivery with micro- and nanoparticles.Advanced materials (Deerfield Beach, Fla.) · 2012
    Review
  12. Review
  13. 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

4 authors at 3 institutions in 1 country.

Matteo PorottoDepartment of Pediatrics, Weill Medical College of Cornell University, New York, New York, United States of America.
Feng Yi
Anne Moscona
David A LaVan
Cornell University · USMaterial Measurement Laboratory · USNational Institute of Standards and Technology · US

Funding

Viral Pathogenesis and TherapeuticsU54AI057158 · NIAID · WADSWORTH CENTER · PI LEVY, DAVID E · 2003 to 2014
$100.8M
NATIONAL CENTER FOR DESIGN:BIOMIMETIC NANOCONDUCTOR(RMI)PN2EY016570 · NEI · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI JAKOBSSON, ERIC G · 2005 to 2009
$6.6M
Mitotic Spindle Assembly & Function in C. elegans - Equipment SupplementR01GM049869 · NIGMS · UNIVERSITY OF OREGON · PI BOWERMAN, BRUCE A · 1994 to 2019
$6.5M
Design of peptide entry inhibitors and delivery systems to target emerging henipaR01AI076335 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI MOSCONA, ANNE · 2009 to 2010
$1.5M
Design of peptide entry inhibitors and delivery systems to target emerging henipaR56AI076335 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI MOSCONA, ANNE · 2008 to 2008
$778k
Bioengineering protocells for a new class of viral vaccinesR21EB011707 · NIBIB · WEILL MEDICAL COLL OF CORNELL UNIV · PI POROTTO, MATTEO · 2011 to 2012
$465k
Novel brain-penetrant fusion inhibitors for control of CNS infection.R21NS076385 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI POROTTO, MATTEO · 2011 to 2012
$443k
NEI NIH HHS 2 PN2 EY016570BNEI NIH HHS PN2 EY016570NIAID NIH HHS R01 AI076335NIAID NIH HHS R56 AI076335NIAID NIH HHS U54 AI057158NIAID NIH HHS U54AI057158NIBIB NIH HHS EB011707NIBIB NIH HHS R21 EB011707NIGMS NIH HHS GM049869NINDS NIH HHS R21 NS076385
6 · The paper itself

Abstract

We present a new antiviral strategy and research tool that could be applied to a wide range of enveloped viruses that infect human beings via membrane fusion. We test this strategy on two emerging zoonotic henipaviruses that cause fatal encephalitis in humans, Nipah (NiV) and Hendra (HeV) viruses. In the new approach, artificial cell-like particles (protocells) presenting membrane receptors in a biomimetic manner were developed and found to attract and inactivate henipavirus envelope glycoprotein pseudovirus particles, preventing infection. The protocells do not accumulate virus during the inactivation process. The use of protocells that interact with, but do not accumulate, viruses may provide significant advantages over current antiviral drugs, and this general approach may have wide potential for antiviral development.

Indexed as

Virus InactivationArtificial CellsCell MembraneHendra VirusHumansMembrane ProteinsNanoparticlesNipah VirusProtein BindingReceptors, VirusSolubilityTemperatureViral ProteinsMembrane ProteinsReceptors, VirusViral Proteins

Identifiers

PMID21390296
PMCPMC3046955
OpenAlexW1990922204

What OpenQuestion holds

Textmetadata
LicenceCC0
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.