Evidence map›Paper›PMID 32669552›Full record

ArticleNature communications2020

A STING-based biosensor affords broad cyclic dinucleotide detection within single living eukaryotic cells.

Alex J Pollock, Shivam A Zaver, Joshua J Woodward

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

28 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. AFrontiers in immunology · 2026
    Article
  6. Article
  7. Article
  8. Chemical disinfection ofFrontiers in microbiology · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. The odyssey of cGAS: From cytosol to nucleus.Cytokine & growth factor reviews · 2023
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article
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 at 1 institution in 1 country.

Alex J Pollock *Department of Microbiology, University of Washington, Seattle, WA, 98195, USA.
Shivam A Zaver *Department of Microbiology, University of Washington, Seattle, WA, 98195, USA.
Joshua J WoodwardDepartment of Microbiology, University of Washington, Seattle, WA, 98195, USA. jjwoodwa@uw.edu.ORCID http://orcid.org/0000-0002-4630-403X
University of Washington · US

Funding

University of Washington Medical Scientist Training Program: MD/PhDT32GM007266 · NIGMS · UNIVERSITY OF WASHINGTON · PI HORWITZ, MARSHALL S. · 1985 to 2023
$30.4M
TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
Viral Pathogenesis Training ProgramT32AI083203 · NIAID · UNIVERSITY OF WASHINGTON · PI BLOOM, JESSE D, LAGUNOFF, MICHAEL · 2009 to 2023
$2.7M
FRET based imaging of cyclic dinucleotide dynamics in living systemsR21AI153820 · NIAID · UNIVERSITY OF WASHINGTON · PI WOODWARD, JOSHUA · 2020 to 2021
$459k
Signal transduction of cGAMP during innate immune responsesR21AI137758 · NIAID · UNIVERSITY OF WASHINGTON · PI WOODWARD, JOSHUA · 2018 to 2019
$429k
The Expanded Repertoire of cGAMP Signal Transduction During Innate Immune ResponsesF30CA239659 · NCI · UNIVERSITY OF WASHINGTON · PI ZAVER, SHIVAM · 2019 to 2021
$97k
NCI NIH HHS F30 CA239659NIAID NIH HHS R21 AI137758NIAID NIH HHS R21 AI153820NIAID NIH HHS T32 AI083203NIGMS NIH HHS T32 GM007266NIGMS NIH HHS T32 GM007270
6 · The paper itself

Abstract

Cyclic dinucleotides (CDNs) are second messengers conserved across all three domains of life. Within eukaryotes they mediate protective roles in innate immunity against malignant, viral, and bacterial disease, and exert pathological effects in autoimmune disorders. Despite their ubiquitous role in diverse biological contexts, CDN detection methods are limited. Here, using structure guided design of the murine STING CDN binding domain, we engineer a Förster resonance energy transfer (FRET) based biosensor deemed BioSTING. Recombinant BioSTING affords real-time detection of CDN synthase activity and inhibition. Expression of BioSTING in live human cells allows quantification of localized bacterial and eukaryotic CDN levels in single cells with low nanomolar sensitivity. These findings establish BioSTING as a powerful kinetic in vitro platform amenable to high throughput screens and as a broadly applicable cellular tool to interrogate the temporal and spatial dynamics of CDN signaling in a variety of infectious, malignant, and autoimmune contexts.

Indexed as

Biosensing TechniquesSignal TransductionAnimalsBacillus subtilisCyclic GMPFlow CytometryFluorescence Resonance Energy TransferHEK293 CellsHumansImmunity, InnateLigandsMembrane ProteinsMiceMutagenesisNucleotides, CyclicProtein DomainsCyclic GMPLigandsMembrane ProteinsNucleotides, CyclicRecombinant ProteinsSTING1 protein, humanSting1 protein, mouseSTING Protein

Identifiers

PMID32669552
PMCPMC7363834
OpenAlexW3043278305

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.