Evidence map›Paper›PMID 23580619›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Visualization of uncorrelated, tandem symmetry mismatches in the internal genome packaging apparatus of bacteriophage T7.

Fei Guo, Zheng Liu, Frank Vago, Yue Ren, Weimin Wu, Elena T Wright, Philip Serwer, Wen Jiang

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Cryo-EM structure of cyanopodophage A4 reveals a pentameric pre-ejectosome in the double-stabilized capsid.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Ejectosome ofPNAS nexus · 2024
    Article
  10. Article
  11. Review
  12. Siphophage 0105phi7-2 ofInternational journal of molecular sciences · 2023
    Article
  13. Article
  14. Review
  15. Review
  16. Structural changes in bacteriophage T7 upon receptor-induced genome ejection.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Assisted assembly of bacteriophage T7 core components for genome translocation across the bacterial envelope.Proceedings of the National Academy of Sciences of the United States of America · 2021
    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

8 authors.

Fei GuoMarkey Center for Structural Biology, Department of Biological Sciences, Purdue University, West Lafayette, IN 47907, USA.
Zheng Liu
Frank Vago
Yue Ren
Weimin Wu
Elena T Wright
Philip Serwer
Wen Jiang

Funding

AN ELECTRON MICROSCOPE FOR THE STUDY OF COMPLEX BIOLOGICAL ASSEMBLIESS10RR023011 · NCRR · PURDUE UNIVERSITY · PI ROSSMANN, MICHAEL G · 2006 to 2006
$2.0M
Structural basis of bacteriophage T7 assembly and DNA packagingR01AI072035 · NIAID · PURDUE UNIVERSITY · PI JIANG, WEN · 2007 to 2011
$1.8M
SINGLE MOLECULE ANALYSIS OF COMPLEX DNA METABOLISMR01GM024365 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI SERWER, PHILIP · 1985 to 2005
$1.1M
NCRR NIH HHS S10 RR023011NCRR NIH HHS S10RR023011NIAID NIH HHS R01 AI072035NIAID NIH HHS R01AI072035NIGMS NIH HHS R01 GM024365NIGMS NIH HHS R01GM24365
6 · The paper itself

Abstract

Motor-driven packaging of a dsDNA genome into a preformed protein capsid through a unique portal vertex is essential in the life cycle of a large number of dsDNA viruses. We have used single-particle electron cryomicroscopy to study the multilayer structure of the portal vertex of the bacteriophage T7 procapsid, the recipient of T7 DNA in packaging. A focused asymmetric reconstruction method was developed and applied to selectively resolve neighboring pairs of symmetry-mismatched layers of the portal vertex. However, structural features in all layers of the multilayer portal vertex could not be resolved simultaneously. Our results imply that layers with mismatched symmetries can join together in several different relative orientations, and that orientations at different interfaces assort independently to produce structural isomers, a process that we call combinatorial assembly isomerism. This isomerism explains rotational smearing in previously reported asymmetric reconstructions of the portal vertex of T7 and other bacteriophages. Combinatorial assembly isomerism may represent a new regime of structural biology in which globally varying structures assemble from a common set of components. Our reconstructions collectively validate previously proposed symmetries, compositions, and sequential order of T7 portal vertex layers, resolving in tandem the 5-fold gene product 10 (gp10) shell, 12-fold gp8 portal ring, and an internal core stack consisting of 12-fold gp14 adaptor ring, 8-fold bowl-shaped gp15, and 4-fold gp16 tip. We also found a small tilt of the core stack relative to the icosahedral fivefold axis and propose that this tilt assists DNA spooling without tangling during packaging.

Indexed as

Models, MolecularBacteriophage T7CapsidCapsid ProteinsCryoelectron MicroscopyEscherichia coliGenome, ViralImaging, Three-DimensionalVirus AssemblyCapsid Proteins

Identifiers

PMID23580619
PMCPMC3637776

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.