Evidence map›Paper›PMID 29997809›Full record

ArticleChemical science2016

High-resolution measurement of long-range distances in RNA: pulse EPR spectroscopy with TEMPO-labeled nucleotides.

Karin Halbmair, Jan Seikowski, Igor Tkach, Claudia Höbartner, Deniz Sezer, Marina Bennati

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
13.6field-weighted citation impact, top 2% 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

22 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Investigating the Conformational Diversity of the TMR-3 Aptamer.Journal of the American Chemical Society · 2025
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  3. Frequency and time domainPhysical chemistry chemical physics : PCCP · 2025
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  5. Review
  6. Article
  7. The Hydrates of TEMPO: Water Vibrations Reveal Radical Microsolvation.Angewandte Chemie (International ed. in English) · 2021
    Article
  8. Article
  9. Covalent labeling of nucleic acids.Chemical Society reviews · 2020
    Review
  10. Orientation and dynamics of CuPhysical chemistry chemical physics : PCCP · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Measurement of Angstrom to Nanometer Molecular Distances withAngewandte Chemie (International ed. in English) · 2020
    Article
  18. Review
  19. "End-to-end" stacking of small dsRNA.RNA (New York, N.Y.) · 2019
    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

6 authors at 3 institutions in 2 countries.

Karin HalbmairMax Planck Institute for Biophysical Chemistry , 37077 Göttingen , Germany . Email: marina.bennati@mpibpc.mpg.de.
Jan SeikowskiMax Planck Institute for Biophysical Chemistry , 37077 Göttingen , Germany . Email: marina.bennati@mpibpc.mpg.de.
Igor TkachMax Planck Institute for Biophysical Chemistry , 37077 Göttingen , Germany . Email: marina.bennati@mpibpc.mpg.de.
Claudia HöbartnerMax Planck Institute for Biophysical Chemistry , 37077 Göttingen , Germany . Email: marina.bennati@mpibpc.mpg.de.
Deniz SezerFaculty of Engineering and Natural Sciences , Sabanci University , 34956 Istanbul , Turkey . Email: dsezer@sabanciuniv.edu.
Marina BennatiMax Planck Institute for Biophysical Chemistry , 37077 Göttingen , Germany . Email: marina.bennati@mpibpc.mpg.de.
Max Planck Institute for Biophysical Chemistry · DEUniversity of Göttingen · DESabancı Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Structural information at atomic resolution of biomolecular assemblies, such as RNA and RNA protein complexes, is fundamental to comprehend biological function. Modern spectroscopic methods offer exceptional opportunities in this direction. Here we present the capability of pulse EPR to report high-resolution long-range distances in RNAs by means of a recently developed spin labeled nucleotide, which carries the TEMPO group directly attached to the nucleobase and preserves Watson-Crick base-pairing. In a representative RNA duplex with spin-label separations up to 28 base pairs (≈8 nm) we demonstrate that the label allows for a model-free conversion of inter-spin distances into base-pair separation (Δbp) if broad-band pulse excitation at Q band frequencies (34 GHz) is applied. The observed distance distribution increases from ±0.2 nm for Δbp = 10 to only ±0.5 nm for Δbp = 28, consistent with only small deviations from the "ideal" A-form RNA structure. Molecular dynamics (MD) simulations conducted at 20 °C show restricted conformational freedom of the label. MD-generated structural deviations from an "ideal" A-RNA geometry help disentangle the contributions of local flexibility of the label and its neighboring nucleobases and global deformations of the RNA double helix to the experimental distance distributions. The study demonstrates that our simple but strategic spin labeling procedure can access detailed structural information on RNAs at atomic resolution over distances that match the size of macromolecular RNA complexes.

Identifiers

PMID29997809
PMCPMC6005265
OpenAlexW2269390754

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Registered trials

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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.