Evidence map›Paper›PMID 21762796›Full record

ReviewJournal of molecular biology2011

Visualizing HIV-1 assembly.

Nolwenn Jouvenet, Sanford M Simon, Paul D Bieniasz

Abstract readReview
In one paragraph

Review in Journal of molecular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. 5'-Cap sequestration is an essential determinant of HIV-1 genome packaging.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Identification of the initial nucleocapsid recognition element in the HIV-1 RNA packaging signal.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  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

3 authors.

Nolwenn JouvenetLaboratory of Retrovirology, The Rockefeller University, New York, NY 10016, USA.
Sanford M Simon
Paul D Bieniasz

Funding

RNA Protein interactions in HIV-1 replicationR01AI050111 · NIAID · ROCKEFELLER UNIVERSITY · PI BIENIASZ, PAUL D. · 2001 to 2021
$7.9M
Mechanism of Action of Retroviral Late-Budding DomainsR01AI052774 · NIAID · AARON DIAMOND AIDS RESEARCH CENTER · PI BIENIASZ, PAUL D. · 2002 to 2011
$3.4M
Biogenesis of HIV 1 in living cellsR01AI089844 · NIAID · ROCKEFELLER UNIVERSITY · PI SIMON, SANFORD M · 2010 to 2013
$1.6M
Selective fluorescent labeling of proteins in living cellsR01GM087977 · NIGMS · ROCKEFELLER UNIVERSITY · PI SIMON, SANFORD M · 2009 to 2012
$1.6M
Dynamic of Retroviruses Assembly and BuddingK99AI087368 · NIAID · AARON DIAMOND AIDS RESEARCH CENTER · PI JOUVENET, NOLWENN MONIQUE · 2010 to 2010
$93k
Howard Hughes Medical InstituteNIAID NIH HHS K99 AI087368NIAID NIH HHS K99AI87368NIAID NIH HHS R01 AI050111NIAID NIH HHS R01 AI052774NIAID NIH HHS R01 AI089844NIAID NIH HHS R01AI50111NIAID NIH HHS R01 AI52774NIGMS NIH HHS R01 GM087977
6 · The paper itself

Abstract

The assembly of an HIV-1 particle is a complex, multistep process involving several viral and cellular proteins, RNAs and lipids. While many macroscopic and fixed-cell microscopic techniques have provided important insights into the structure of HIV-1 particles and the mechanisms by which they assemble, analysis of individual particles and their assembly in living cells offers the potential of surmounting many of the limitations inherent in other approaches. In this review, we discuss how the recent application of live-cell microscopic imaging techniques has increased our understanding of the process of HIV-1 particle assembly. In particular, we focus on recent studies that have employed total internal reflection fluorescence microscopy and other single-virion imaging techniques in live cells. These approaches have illuminated the dynamics of Gag protein assembly, viral RNA packaging and ESCRT (endosomal sorting complex required for transport) protein recruitment at the level of individual viral particles. Overall, the particular advantages of individual particle imaging in living cells have yielded findings that would have been difficult or impossible to obtain using macroscopic or fixed-cell microscopic techniques.

Indexed as

HIV-1HumansImaging, Three-DimensionalMicroscopyVirionVirus Assembly

Identifiers

PMID21762796
PMCPMC3144478

What OpenQuestion holds

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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.