Evidence map›Paper›PMID 30249401›Full record

ArticleBiophysical journal2018

Mechanics of Virus-like Particles Labeled with Green Fluorescent Protein.

Johann Mertens, Patricia Bondia, Carolina Allende-Ballestero, José L Carrascosa, Cristina Flors, José R Castón

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 3 institutions in 1 country.

Johann MertensMadrid Institute for Advanced Studies in Nanoscience (IMDEA Nanoscience), Madrid, Spain.
Patricia BondiaMadrid Institute for Advanced Studies in Nanoscience (IMDEA Nanoscience), Madrid, Spain; Nanobiotechnology Associated Unit CNB-CSIC-IMDEA, Campus de Cantoblanco, Madrid, Spain.
Carolina Allende-BallesteroDepartment of Structure of Macromolecules, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
José L CarrascosaDepartment of Structure of Macromolecules, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain; Nanobiotechnology Associated Unit CNB-CSIC-IMDEA, Campus de Cantoblanco, Madrid, Spain.
Cristina FlorsMadrid Institute for Advanced Studies in Nanoscience (IMDEA Nanoscience), Madrid, Spain; Nanobiotechnology Associated Unit CNB-CSIC-IMDEA, Campus de Cantoblanco, Madrid, Spain. Electronic address: cristina.flors@imdea.org.
José R CastónDepartment of Structure of Macromolecules, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain; Nanobiotechnology Associated Unit CNB-CSIC-IMDEA, Campus de Cantoblanco, Madrid, Spain. Electronic address: jrcaston@cnb.csic.es.
Madrid Institute for Advanced Studies · ESCentro Nacional de Biotecnología · ESIMDEA Nanoscience · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoindentation with an atomic force microscope was used to investigate the mechanical properties of virus-like particles (VLPs) derived from the avian pathogen infectious bursal disease virus, in which the major capsid protein was modified by fusion with enhanced green fluorescent protein (EGFP). These VLPs assemble as ∼70-nm-diameter T = 13 icosahedral capsids with large cargo space. The effect of the insertion of heterologous proteins in the capsid was characterized in the elastic regime, revealing that EGFP-labeled chimeric VLPs are more rigid than unmodified VLPs. In addition, nanoindentation measurements beyond the elastic regime allowed the determination of brittleness and rupture force limit. EGFP incorporation results in a complex shape of the indentation curve and lower critical indentation depth of the capsid, rendering more brittle particles as compared to unlabeled VLPs. These observations suggest the presence of a complex and more constrained network of interactions between EGFP and the capsid inner shell. These results highlight the effect of fluorescent protein insertion on the mechanical properties of these capsids. Because the physical properties of the viral capsid are connected to viral infectivity and VLP transport and disassembly, our results are relevant to design improved labeling strategies for fluorescence tracking in living cells.

Indexed as

Virus AssemblyAnimalsBaculoviridaeCells, CulturedGreen Fluorescent ProteinsRecombinant Fusion ProteinsViral Structural ProteinsVirionenhanced green fluorescent proteinGreen Fluorescent ProteinsRecombinant Fusion ProteinsViral Structural ProteinsVP2 protein, infectious bursal disease virus

Identifiers

PMID30249401
PMCPMC6260219
OpenAlexW2888881577

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.