Evidence map›Paper›PMID 22404932›Full record

ArticleBiophysical journal2012

Thermodynamic and kinetic analysis of an RNA kissing interaction and its resolution into an extended duplex.

Nilshad Salim, Rajan Lamichhane, Rui Zhao, Tuhina Banerjee, Jane Philip, David Rueda, Andrew L Feig

Abstract read
In one paragraph

Article in Biophysical journal, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Trapping Transient RNA Complexes by Chemically Reversible Acylation.Angewandte Chemie (International ed. in English) · 2020
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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  15. 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

7 authors.

Nilshad SalimDepartment of Chemistry, Wayne State University, Detroit, Michigan, USA.
Rajan Lamichhane
Rui Zhao
Tuhina Banerjee
Jane Philip
David Rueda
Andrew L Feig

Funding

Single Molecule Study of Spliceosomal RNAsR01GM085116 · NIGMS · WAYNE STATE UNIVERSITY · PI CHOW, CHRISTINE S · 2008 to 2012
$1.3M
RNA Cold DenaturationR01GM065430 · NIGMS · WAYNE STATE UNIVERSITY · PI FEIG, ANDREW L · 2003 to 2007
$1.1M
Investigations of Hfq-RNA InteractionsR01GM075068 · NIGMS · WAYNE STATE UNIVERSITY · PI FEIG, ANDREW L · 2005 to 2008
$931k
NIGMS NIH HHS GM065430NIGMS NIH HHS GM075068NIGMS NIH HHS GM085116NIGMS NIH HHS R01 GM065430NIGMS NIH HHS R01 GM075068NIGMS NIH HHS R01 GM085116
6 · The paper itself

Abstract

Kissing hairpin interactions form when the loop residues of two hairpins have Watson-Crick complementarity. In a unimolecular context, kissing interactions are important for tertiary folding and pseudoknot formation, whereas in a bimolecular context, they provide a basis for molecular recognition. In some cases, kissing complexes can be a prelude to strand displacement reactions where the two hairpins resolve to form a stable extended intermolecular duplex. The kinetics and thermodynamics of kissing-complex formation and their subsequent strand-displacement reactions are poorly understood. Here, biophysical techniques including isothermal titration calorimetry, surface plasmon resonance, and single-molecule fluorescence have been employed to probe the factors that govern the stability of kissing complexes and their subsequent structural rearrangements. We show that the general understanding of RNA duplex formation can be extended to kissing complexes but that kissing complexes display an unusual level of stability relative to simple duplexes of the same sequence. These interactions form and break many times at room temperature before becoming committed to a slow, irreversible forward transition to the strand-displaced form. Furthermore, using smFRET we show that the primary difference between stable and labile kissing complexes is based almost completely on their off rates. Both stable and labile complexes form at the same rate within error, but less stable species dissociate rapidly, allowing us to understand how these complexes can help generate specificity along a folding pathway or during a gene regulation event.

Indexed as

Inverted Repeat SequencesBase SequenceCalorimetryFluorescence Resonance Energy TransferKineticsMutationRNA, Double-StrandedThermodynamicsRNA, Double-Stranded

Identifiers

PMID22404932
PMCPMC3296049

What OpenQuestion holds

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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.