Evidence map›Paper›PMID 18400780›Full record

ArticleNucleic acids research2008

Structural probing of the HIV-1 polypurine tract RNA:DNA hybrid using classic nucleic acid ligands.

Kevin B Turner, Robert G Brinson, Hye Young Yi-Brunozzi, Jason W Rausch, Jennifer T Miller, Stuart F J Le Grice, John P Marino, Daniele Fabris

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Targeting the HIV RNA genome: high-hanging fruit only needs a longer ladder.Current topics in microbiology and immunology · 2015
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. A role for the MS analysis of nucleic acids in the post-genomics age.Journal of the American Society for Mass Spectrometry · 2010
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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 at 3 institutions in 1 country.

Kevin B TurnerUniversity of Maryland Baltimore County, Baltimore, MD, USA.
Robert G Brinson
Hye Young Yi-Brunozzi
Jason W Rausch
Jennifer T Miller
Stuart F J Le Grice
John P Marino
Daniele Fabris
National Institutes of Health · USUniversity of Maryland, Baltimore County · USNational Institute of Standards and Technology · US

Funding

Nucleic Acid Footprinting and development of small molecule antagonistsZIABC010493 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LE GRICE, STUART F. J. · 2009 to 2021
$9.3M
STRUCTURAL BASIS OF RNA STEM LOOP KISSING INTERACTIONSR01GM059107 · NIGMS · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI MARINO, JOHN PAUL · 1999 to 2008
$1.7M
Intramural NIH HHSNIGMS NIH HHS GM59107NIGMS NIH HHS GM643208NIGMS NIH HHS R01 GM059107
6 · The paper itself

Abstract

The interactions of archetypical nucleic acid ligands with the HIV-1 polypurine tract (PPT) RNA:DNA hybrid, as well as analogous DNA:DNA, RNA:RNA and swapped hybrid substrates, were used to probe structural features of the PPT that contribute to its specific recognition and processing by reverse transcriptase (RT). Results from intercalative and groove-binding ligands indicate that the wild-type PPT hybrid does not contain any strikingly unique groove geometries and/or stacking arrangements that might contribute to the specificity of its interaction with RT. In contrast, neomycin bound preferentially and selectively to the PPT near the 5'(rA)(4):(dT)(4) tract and the 3' PPT-U3 junction. Nuclear magnetic resonance data from a complex between HIV-1 RT and the PPT indicate RT contacts within the same regions highlighted on the PPT by neomycin. These observations, together with the fact that the sites are correctly spaced to allow interaction with residues in the ribonuclease H (RNase H) active site and thumb subdomain of the p66 RT subunit, suggest that despite the long cleft employed by RT to make contact with nucleic acids substrates, these sites provide discrete binding units working in concert to determine not only specific PPT recognition, but also its orientation on the hybrid structure.

Indexed as

AminoglycosidesBinding SitesDNA, ViralFramycetinHIV-1LigandsMass SpectrometryNuclear Magnetic Resonance, BiomolecularNucleic Acid ProbesPurinesRNA, ViralThermodynamicsAminoglycosidesDNA, ViralFramycetinLigandsNucleic Acid ProbesPurinesRNA, Viral

Identifiers

PMID18400780
PMCPMC2377446
OpenAlexW2119143098

What OpenQuestion holds

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LicenceCC BY-NC
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.