Evidence map›Paper›PMID 24586236›Full record

ArticlePloS one2014

Mapping the kinetic barriers of a Large RNA molecule's folding landscape.

Jörg C Schlatterer, Joshua S Martin, Alain Laederach, Michael Brenowitz

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. RNA Modeling with the Computational Energy Landscape Framework.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  3. Review
  4. Understanding the kinetic mechanism of RNA single base pair formation.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  5. 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

4 authors.

Jörg C SchlattererDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Joshua S MartinNational Evolutionary Synthesis Center, Durham, North Carolina, United States of America ; Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Alain LaederachDepartment of Biology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Michael BrenowitzDepartment of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, United States of America.

Funding

Non-coding RNA structure change in Chronic Obstructive Pulmonary DiseaseR01HL111527 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Alain T Laederach, Kevin M Weeks · 2012 to 2026
$6.6M
Structural and functional consequences of disease SNPs on the transcriptomeR01GM101237 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LAEDERACH, ALAIN T · 2012 to 2020
$2.5M
Towards solution of the RNA folding problemR01GM085130 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BRENOWITZ, MICHAEL D. · 2009 to 2012
$1.4M
NHLBI NIH HHS R01 HL111527NHLBI NIH HHS R01-HL111527NIGMS NIH HHS 1R01-GM085130NIGMS NIH HHS R01 GM085130NIGMS NIH HHS R01 GM101237NIGMS NIH HHS R01- GM101237
6 · The paper itself

Abstract

The folding of linear polymers into discrete three-dimensional structures is often required for biological function. The formation of long-lived intermediates is a hallmark of the folding of large RNA molecules due to the ruggedness of their energy landscapes. The precise thermodynamic nature of the barriers (whether enthalpic or entropic) that leads to intermediate formation is still poorly characterized in large structured RNA molecules. A classic approach to analyzing kinetic barriers are temperature dependent studies analyzed with Eyring's transition state theory. We applied Eyring's theory to time-resolved hydroxyl radical (•OH) footprinting kinetics progress curves collected at eight temperature from 21.5 °C to 51 °C to characterize the thermodynamic nature of folding intermediate formation for the Mg(2+)-mediated folding of the Tetrahymena thermophila group I ribozyme. A common kinetic model configuration describes this RNA folding reaction over the entire temperature range studied consisting of primary (fast) transitions to misfolded intermediates followed by much slower secondary transitions, consistent with previous studies. Eyring analysis reveals that the primary transitions are moderate in magnitude and primarily enthalpic in nature. In contrast, the secondary transitions are daunting in magnitude and entropic in nature. The entropic character of the secondary transitions is consistent with structural rearrangement of the intermediate species to the final folded form. This segregation of kinetic control reveals distinctly different molecular mechanisms during the two stages of RNA folding and documents the importance of entropic barriers to defining rugged RNA folding landscapes.

Indexed as

Base SequenceHydroxyl RadicalKineticsMagnesiumMolecular Sequence DataNucleic Acid ConformationRNA, CatalyticRNA FoldingRNA, ProtozoanTemperatureTetrahymena thermophilaThermodynamicsGIR1 ribozymeHydroxyl RadicalMagnesiumRNA, CatalyticRNA, Protozoan

Identifiers

PMID24586236
PMCPMC3934814

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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.