Evidence map›Paper›PMID 21281578›Full record

ArticleBiophysical journal2011

Bending and puncturing the influenza lipid envelope.

Sai Li, Frederic Eghiaian, Christian Sieben, Andreas Herrmann, Iwan A T Schaap

Abstract read
In one paragraph

Article in Biophysical journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Force spectroscopy reveals membrane fluctuations and surface adhesion of extracellular nanovesicles impact their elastic behavior.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Extracellular vesicle-matrix interactions.Nature reviews. Materials · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Invariant in variants.Ultrasonics · 2022
    Article
  16. Nanoparticle-blockage-enabled rapid and reversible nanopore gating with tunable memory.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. 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.

Sai LiDrittes Physikalisches Institut, Georg-August-Universität, Göttingen, Germany.
Frederic EghiaianDrittes Physikalisches Institut, Georg-August-Universität, Göttingen, Germany. Electronic address: feghiai@physik3.gwdg.de.
Christian SiebenInstitut für Biologie, Humboldt-Universität zu Berlin, Berlin, Germany.
Andreas HerrmannInstitut für Biologie, Humboldt-Universität zu Berlin, Berlin, Germany.
Iwan A T SchaapDrittes Physikalisches Institut, Georg-August-Universität, Göttingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lysosomes, enveloped viruses, as well as synaptic and secretory vesicles are all examples of natural nanocontainers (diameter ≈ 100 nm) which specifically rely on their lipid bilayer to protect and exchange their contents with the cell. We have applied methods primarily based on atomic force microscopy and finite element modeling that allow precise investigation of the mechanical properties of the influenza virus lipid envelope. The mechanical properties of small, spherical vesicles made from PR8 influenza lipids were probed by an atomic force microscopy tip applying forces up to 0.2 nN, which led to an elastic deformation up to 20%, on average. The liposome deformation was modeled using finite element methods to extract the lipid bilayer elastic properties. We found that influenza liposomes were softer than what would be expected for a gel phase bilayer and highly deformable: Consistent with previous suggestion that influenza lipids do not undergo a major phase transition, we observe that the stiffness of influenza liposomes increases gradually and weakly (within one order of magnitude) with temperature. Surprisingly, influenza liposomes were, in most cases, able to withstand wall-to-wall deformation, and forces >1 nN were generally required to puncture the influenza envelope, which is similar to viral protein shells. Hence, the choice of a highly flexible lipid envelope may provide as efficient a protection for a viral genome as a stiff protein shell.

Indexed as

Biomechanical PhenomenaDimyristoylphosphatidylcholineLipid BilayersLiposomesMicroscopy, Atomic ForceOrthomyxoviridaeTemperatureDimyristoylphosphatidylcholineLipid BilayersLiposomes

Identifiers

PMID21281578
PMCPMC3030173

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.