Evidence map›Paper›PMID 30773480›Full record

ArticleCell chemical biology2019

Detection of Low-Abundance Metabolites in Live Cells Using an RNA Integrator.

Mingxu You, Jacob L Litke, Rigumula Wu, Samie R Jaffrey

Open access · bronzeAbstract read
In one paragraph

Article in Cell chemical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Artificial dynamic structure ensemble-guided rational design of a universal RNA aptamer-based sensing tag.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Ribocentre: a database of ribozymes.Nucleic acids research · 2023
    Article
  12. Assembly of long L-RNA by native RNA ligation.Chemical communications (Cambridge, England) · 2021
    Article
  13. Review
  14. Review
  15. Article
  16. Paper-based fluorogenic RNA aptamer sensors for label-free detection of small molecules.Analytical methods : advancing methods and applications · 2020
    Article
  17. Review
  18. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Mingxu YouDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA; Department of Pharmacology, Weill Medical College, Weill Cornell Medicine, New York, NY 10065, USA. Electronic address: mingxuyou@umass.edu.
Jacob L LitkeDepartment of Pharmacology, Weill Medical College, Weill Cornell Medicine, New York, NY 10065, USA.
Rigumula WuDepartment of Chemistry, University of Massachusetts, Amherst, MA 01003, USA.
Samie R JaffreyDepartment of Pharmacology, Weill Medical College, Weill Cornell Medicine, New York, NY 10065, USA. Electronic address: srj2003@med.cornell.edu.
Cornell University · USUniversity of Massachusetts Amherst · US

Funding

Engineering RNA-activated fluorescence switches for RNA imaging and analyte sensiR01NS064516 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI JAFFREY, SAMIE R · 2009 to 2018
$3.6M
Genetically-encoded fluorescent RNA sensors for measuring transport of antibiotics into the cytoplasm of Gram-negative pathogens and development of efflux pump inhibitorsR01AI136789 · NIAID · HARVARD MEDICAL SCHOOL · PI LORY, STEPHEN · 2018 to 2022
$3.6M
Novel fluorescent sensors for simple, sensitive, and specific protein detectionR01EB010249 · NIBIB · WEILL MEDICAL COLL OF CORNELL UNIV · PI JAFFREY, SAMIE R · 2009 to 2013
$1.7M
NIAID NIH HHS R01 AI136789NIBIB NIH HHS R01 EB010249NINDS NIH HHS R01 NS064516
6 · The paper itself

Abstract

Genetically encoded biosensors are useful tools for detecting the presence and levels of diverse biomolecules in living cells. However, low-abundance targets are difficult to detect because they are often unable to bind and activate enough biosensors to detect using standard microscopic imaging approaches. Here we describe a type of RNA-based biosensor, an RNA integrator, which enables detection of low-abundance targets in vitro and in living cells. The RNA integrator is an RNA sequence comprising a ribozyme and an unfolded form of the fluorogenic aptamer Broccoli. Upon binding its target, the ribozyme undergoes cleavage and releases Broccoli, which subsequently folds and becomes fluorescent. Importantly, each target molecule can bind and induce cleavage of multiple copies of the integrator sensor, resulting in an amplified signal. We show that this approach can be generalized to numerous different ribozyme types for the detection of various small molecules.

Indexed as

Aptamers, NucleotideBase SequenceBiosensing TechniquesEscherichia coliFluorescent DyesOptical ImagingRNA, CatalyticRNA FoldingAptamers, NucleotideFluorescent DyesRNA, Catalyticcellular imagingfluorescencefluorogenic aptamerlow-abundance metaboliteribozymeRNA probes

Identifiers

PMID30773480
PMCPMC6474789
OpenAlexW2912937049

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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.