Evidence map›Paper›PMID 33919831›Full record

ReviewMolecules (Basel, Switzerland)2021

RNA Proximity Labeling: A New Detection Tool for RNA-Protein Interactions.

Ronja Weissinger, Lisa Heinold, Saira Akram, Ralf-Peter Jansen, Orit Hermesh

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Proteomic Technology.Advances in experimental medicine and biology · 2026
    Review
  6. Article
  7. CRISPR RiPCA for Investigating eIF4E-mACS chemical biology · 2025
    Article
  8. APEX2 proximity labeling of RNA in bacteria.bioRxiv : the preprint server for biology · 2025
    Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Frontiers in molecular biosciences · 2022
    Article
  18. Review
  19. 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

5 authors at 1 institution in 1 country.

Ronja WeissingerInterfaculty Institute for Biochemistry (IFIB), Tübingen University, 72076 Tübingen, Germany.
Lisa HeinoldInterfaculty Institute for Biochemistry (IFIB), Tübingen University, 72076 Tübingen, Germany.
Saira AkramInterfaculty Institute for Biochemistry (IFIB), Tübingen University, 72076 Tübingen, Germany.
Ralf-Peter JansenInterfaculty Institute for Biochemistry (IFIB), Tübingen University, 72076 Tübingen, Germany.
Orit HermeshInterfaculty Institute for Biochemistry (IFIB), Tübingen University, 72076 Tübingen, Germany.
University of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple cellular functions are controlled by the interaction of RNAs and proteins. Together with the RNAs they control, RNA interacting proteins form RNA protein complexes, which are considered to serve as the true regulatory units for post-transcriptional gene expression. To understand how RNAs are modified, transported, and regulated therefore requires specific knowledge of their interaction partners. To this end, multiple techniques have been developed to characterize the interaction between RNAs and proteins. In this review, we briefly summarize the common methods to study RNA-protein interaction including crosslinking and immunoprecipitation (CLIP), and aptamer- or antisense oligonucleotide-based RNA affinity purification. Following this, we focus on in vivo proximity labeling to study RNA-protein interactions. In proximity labeling, a labeling enzyme like ascorbate peroxidase or biotin ligase is targeted to specific RNAs, RNA-binding proteins, or even cellular compartments and uses biotin to label the proteins and RNAs in its vicinity. The tagged molecules are then enriched and analyzed by mass spectrometry or RNA-Seq. We highlight the latest studies that exemplify the strength of this approach for the characterization of RNA protein complexes and distribution of RNAs in vivo.

Indexed as

Staining and LabelingBiotinProtein BindingRNARNA-Binding ProteinsTranscriptomeBiotinRNARNA-Binding Proteinsascorbate peroxidasebiotin ligaseproximity labelingRNA-binding proteinRNA–protein complexsubcellular transcriptomics

Identifiers

PMID33919831
PMCPMC8070807
OpenAlexW3154776405

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.