Evidence map›Paper›PMID 12853646›Full record

ArticleNucleic acids research2003

Molecular dynamics reveals the stabilizing role of loop closing residues in kissing interactions: comparison between TAR-TAR* and TAR-aptamer.

François Beaurain, Carmelo Di Primo, Jean Jacques Toulmé, Michel Laguerre

Abstract read
In one paragraph

Article in Nucleic acids research, 2003. 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
–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

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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  9. Self-association of adenine-dependent hairpin ribozymes.European biophysics journal : EBJ · 2008
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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

4 authors.

François BeaurainInstitut Européen de Chimie et Biologie, CNRS UMR 5144, 16 Avenue Pey Berland, F-33607 Pessac Cedex, France. f.beaurain@iecb-polytechnique.u-bordeaux.fr
Carmelo Di Primo
Jean Jacques Toulmé
Michel Laguerre

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A RNA aptamer (R06) raised against the trans- activation responsive (TAR) element of HIV-1 was previously shown to generate a loop-loop complex whose stability is strongly dependent on the selected G and A residues closing the aptamer loop. The rationally designed TAR* RNA hairpin with a loop sequence fully complementary to the TAR element, closed by U,A residues, also engages in a loop-loop association with TAR, but with a lower stability compared with the TAR-R06 complex. UV absorption monitored thermal denaturation showed that TAR-TAR*(GA), in which the U,A kissing residues were exchanged for G,A, is as stable as the selected TAR-R06 complex. Consequently, we used the TAR-TAR* structure deduced from NMR studies to model the TAR-R06 complex with either GA, CA or UA loop closing residues. The results of the molecular dynamics trajectories correlate well with the thermal denaturation experiments and show that the increased stability of the GA variant results from an optimized stacking of the bases at the stem-loop junction and from stable interbackbone hydrogen bonds.

Indexed as

Nucleic Acid ConformationBase PairingComputer SimulationHIV-1HIV Long Terminal RepeatHumansHydrogen BondingMolecular StructureNucleic Acid DenaturationOligoribonucleotidesRNA, ViralTemperatureOligoribonucleotidesRNA, Viral

Identifiers

PMID12853646
PMCPMC165981

What OpenQuestion holds

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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.