Evidence map›Paper›PMID 19559731›Full record

ArticleJournal of virological methods2009

Monitoring of HIV-1 envelope-mediated membrane fusion using modified split green fluorescent proteins.

Jianqi Wang, Naoyuki Kondo, Yufei Long, Aikichi Iwamoto, Zene Matsuda

Abstract read
In one paragraph

Article in Journal of virological methods, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Development of a rapid cell-fusion-based phenotypic HIV-1 tropism assay.Journal of the International AIDS Society · 2013
    Article
  8. Article
  9. Article
  10. 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

5 authors.

Jianqi WangChina-Japan Joint Laboratory of Structural Virology and Immunology, Institute of Biophysics, Chinese Academy of Sciences, Chaoyang District, Beijing, China.
Naoyuki Kondo
Yufei Long
Aikichi Iwamoto
Zene Matsuda

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A simple, cell-based, membrane fusion assay system that uses split green fluorescent proteins (spGFPs) as an indicator was developed. The attachment of the pleckstrin homology (PH) domain to the N-termini of each spGFP not only localized the reporter signal to the plasma membrane but also helped the stable expression of the smaller spGFP of seventeen amino acid residues. It was shown that this system allowed real-time monitoring of membrane fusion by HIV-1 envelope protein (Env) without the addition of external substrates. This method can be adapted to the analyses of other viral membrane fusion.

Indexed as

Amino Acid SequenceBase SequenceCell Lineenv Gene Products, Human Immunodeficiency VirusGreen Fluorescent ProteinsHIV-1HIV Envelope Protein gp41HIV Fusion InhibitorsHIV InfectionsHumansMembrane FusionMolecular Sequence DataPeptide FragmentsVirologyenv Gene Products, Human Immunodeficiency VirusGreen Fluorescent ProteinsHIV Envelope Protein gp41HIV Fusion Inhibitorspeptide C34Peptide Fragments

Identifiers

PMID19559731
PMCPMC7112932

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.