Evidence map›Paper›PMID 35128480›Full record

ArticleSTAR protocols2022

Analysis of RNA-containing compartments by hybridization and proximity labeling in cultured human cells.

Karen Yap, Tek Hong Chung, Eugene V Makeyev

Abstract read
In one paragraph

Article in STAR protocols, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. 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

3 authors.

Karen YapCentre for Developmental Neurobiology, New Hunt's House, 4.28, King's College London, London SE1 1UL, UK.
Tek Hong ChungCentre for Developmental Neurobiology, New Hunt's House, 4.28, King's College London, London SE1 1UL, UK.
Eugene V MakeyevCentre for Developmental Neurobiology, New Hunt's House, 4.28, King's College London, London SE1 1UL, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/M001199/1Biotechnology and Biological Sciences Research Council BB/M007103/1Biotechnology and Biological Sciences Research Council BB/R001049/1
6 · The paper itself

Abstract

This protocol describes a hybridization-proximity labeling (HyPro) approach for identification of proteins and RNAs co-localizing with a transcript of interest in genetically unperturbed cells. It outlines steps required for purification of a recombinant HyPro enzyme, hybridization of fixed and permeabilized cells with digoxigenin-labeled probes, HyPro enzyme binding, proximity biotinylation, and downstream analyses of the biotinylated products. Although the protocol is optimized for relatively abundant noncoding transcripts, recommendations are provided for improving the signal-to-noise ratio in case of scarcer RNA "baits." For complete details on the use and execution of this protocol, please refer to Yap et al. (2021).

Indexed as

RNABiotinylationCell LineCells, CulturedDigoxigeninHumansDigoxigeninRNACell BiologyGene ExpressionIn Situ HybridizationMass SpectrometryMicroscopyMolecular BiologyMolecular/Chemical ProbesProtein BiochemistryProtein expression and purification

Identifiers

PMID35128480
PMCPMC8808287

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.