Evidence map›Paper›PMID 32839320›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

RNA-protein interaction mapping via MS2- or Cas13-based APEX targeting.

Shuo Han, Boxuan Simen Zhao, Samuel A Myers, Steven A Carr, Chuan He, Alice Y Ting

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
8.3field-weighted citation impact, top 1% 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

104 citing papers in PubMed, 164 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Reprogramming mRNA localization by targeted RNA-protein interference.bioRxiv : the preprint server for biology · 2026
    Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review

44 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Shuo HanDepartment of Genetics, Chan Zuckerberg Biohub, Stanford University, Stanford, CA 94305.
Boxuan Simen ZhaoDepartment of Genetics, Chan Zuckerberg Biohub, Stanford University, Stanford, CA 94305.
Samuel A MyersThe Broad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, MA 02142.
Steven A CarrThe Broad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, MA 02142.
Chuan HeDepartment of Chemistry, Institute for Biophysical Dynamics, Howard Hughes Medical Institute, University of Chicago, Chicago, IL 60637.
Alice Y TingDepartment of Genetics, Chan Zuckerberg Biohub, Stanford University, Stanford, CA 94305; ayting@stanford.edu.
Stanford University · USBroad Institute · USHarvard University · USHoward Hughes Medical Institute · US

Funding

Mapping protein communication between organs in homeostasis and diseaseR01DK121409 · NIDDK · HARVARD MEDICAL SCHOOL · PI CARR, STEVEN A, MCMAHON, ANDREW P. · 2018 to 2022
$8.3M
MICROSCALED PROTEOGENOMICS FOR CANCER CLINICAL TRIALSU01CA214125 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ANURAG, MEENAKSHI, CARR, STEVEN A · 2017 to 2021
$7.0M
Center of Excellence for High Throughput Proteogenomic CharacterizationU24CA210986 · NCI · BROAD INSTITUTE, INC. · PI CARR, STEVEN A, GILLETTE, MICHAEL A · 2016 to 2020
$6.4M
NCI NIH HHS U01 CA214125NCI NIH HHS U24 CA210986NIDDK NIH HHS R01 DK121409
6 · The paper itself

Abstract

RNA-protein interactions underlie a wide range of cellular processes. Improved methods are needed to systematically map RNA-protein interactions in living cells in an unbiased manner. We used two approaches to target the engineered peroxidase APEX2 to specific cellular RNAs for RNA-centered proximity biotinylation of protein interaction partners. Both an MS2-MCP system and an engineered CRISPR-Cas13 system were used to deliver APEX2 to the human telomerase RNA hTR with high specificity. One-minute proximity biotinylation captured candidate binding partners for hTR, including more than a dozen proteins not previously linked to hTR. We validated the interaction between hTR and the

Indexed as

AlkB Homolog 5, RNA DemethylaseBiotinylationCRISPR-Cas SystemsDNA-(Apurinic or Apyrimidinic Site) LyaseDNA MethylationEndonucleasesHEK293 CellsHumansMass SpectrometryMultifunctional EnzymesProtein BindingProtein Interaction MappingRNATelomeraseALKBH5 protein, humanAlkB Homolog 5, RNA DemethylaseAPEX2 protein, humanDNA-(Apurinic or Apyrimidinic Site) LyaseEndonucleasesMultifunctional EnzymesRNATelomerasetelomerase RNAAPEXinteractomeproximity labelingRNA binding proteintelomerase RNA

Identifiers

PMID32839320
PMCPMC7486720
OpenAlexW3080530457

What OpenQuestion holds

Textmetadata
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.