Evidence map›Paper›PMID 32451442›Full record

ArticleNature protocols2020

Visualizing the functional 3D shape and topography of long noncoding RNAs by single-particle atomic force microscopy and in-solution hydrodynamic techniques.

Tina Uroda, Isabel Chillón, Paolo Annibale, Jean-Marie Teulon, Ombeline Pessey, Manikandan Karuppasamy, Jean-Luc Pellequer, Marco Marcia

Abstract read
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In one paragraph

Article in Nature protocols, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Noncoding RNAs: biology and applications-a Keystone Symposia report.Annals of the New York Academy of Sciences · 2021
    Review
  10. Article
  11. Article
  12. Review
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.

Tina UrodaEuropean Molecular Biology Laboratory (EMBL) Grenoble, Grenoble, France.
Isabel ChillónEuropean Molecular Biology Laboratory (EMBL) Grenoble, Grenoble, France.ORCID http://orcid.org/0000-0002-3107-8738
Paolo AnnibaleMax Delbruck Center, Berlin, Germany.
Jean-Marie TeulonUniversité Grenoble Alpes, CEA, CNRS, Institut de Biologie Structurale (IBS), Grenoble, France.
Ombeline PesseyEuropean Molecular Biology Laboratory (EMBL) Grenoble, Grenoble, France.
Manikandan KaruppasamyEuropean Molecular Biology Laboratory (EMBL) Grenoble, Grenoble, France.
Jean-Luc PellequerUniversité Grenoble Alpes, CEA, CNRS, Institut de Biologie Structurale (IBS), Grenoble, France.ORCID http://orcid.org/0000-0002-8944-2715
Marco MarciaEuropean Molecular Biology Laboratory (EMBL) Grenoble, Grenoble, France. mmarcia@embl.fr.ORCID http://orcid.org/0000-0003-2430-0713

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) are recently discovered transcripts that regulate vital cellular processes, such as cellular differentiation and DNA replication, and are crucially connected to diseases. Although the 3D structures of lncRNAs are key determinants of their function, the unprecedented molecular complexity of lncRNAs has so far precluded their 3D structural characterization at high resolution. It is thus paramount to develop novel approaches for biochemical and biophysical characterization of these challenging targets. Here, we present a protocol that integrates non-denaturing lncRNA purification with in-solution hydrodynamic analysis and single-particle atomic force microscopy (AFM) imaging to produce highly homogeneous lncRNA preparations and visualize their 3D topology at ~15-Å resolution. Our protocol is suitable for imaging lncRNAs in biologically active conformations and for measuring structural defects of functionally inactive mutants that have been identified by cell-based functional assays. Once optimized for the specific target lncRNA of choice, our protocol leads from cloning to AFM imaging within 3-4 weeks and can be implemented using state-of-the-art biochemical and biophysical instrumentation by trained researchers familiar with RNA handling and supported by AFM and small-angle X-ray scattering (SAXS) experts.

Indexed as

HydrodynamicsImage Processing, Computer-AssistedMicroscopy, Atomic ForceRNA, Long NoncodingRNA, Long Noncoding

Identifiers

What OpenQuestion holds

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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.