Evidence map›Paper›PMID 31110281›Full record

ArticleNature methods2019

A general method to quantify ligand-driven oligomerization from fluorescence-based images.

Michael R Stoneman, Gabriel Biener, Richard J Ward, John D Pediani, Dammar Badu, Annie Eis, Ionel Popa, Graeme Milligan, Valerică Raicu

Abstract read
In one paragraph

Article in Nature methods, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Intensity-Based Estimation of Monomeric Brightness for Fluorescent Proteins.International journal of molecular sciences · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Diffusion and Oligomerization States of the Muscarinic MThe journal of physical chemistry. B · 2024
    Article
  16. Article
  17. Article
  18. The β2-adrenergic receptor associates with CXCR4 multimers in human cancer cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Michael R StonemanPhysics Department, University of Wisconsin-Milwaukee, Milwaukee, WI, USA.
Gabriel BienerPhysics Department, University of Wisconsin-Milwaukee, Milwaukee, WI, USA.
Richard J WardCentre for Translational Pharmacology, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
John D PedianiCentre for Translational Pharmacology, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0001-6615-537X
Dammar BaduPhysics Department, University of Wisconsin-Milwaukee, Milwaukee, WI, USA.
Annie EisPhysics Department, University of Wisconsin-Milwaukee, Milwaukee, WI, USA.
Ionel PopaPhysics Department, University of Wisconsin-Milwaukee, Milwaukee, WI, USA.ORCID http://orcid.org/0000-0003-3111-4716
Graeme MilliganCentre for Translational Pharmacology, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.ORCID http://orcid.org/0000-0002-6946-3519
Valerică RaicuPhysics Department, University of Wisconsin-Milwaukee, Milwaukee, WI, USA. vraicu@uwm.edu.ORCID http://orcid.org/0000-0002-3427-8516

Funding

Medical Research Council MR/L023806/1
6 · The paper itself

Abstract

Here, we introduce fluorescence intensity fluctuation spectrometry for determining the identity, abundance and stability of protein oligomers. This approach was tested on monomers and oligomers of known sizes and was used to uncover the oligomeric states of the epidermal growth factor receptor and the secretin receptor in the presence and absence of their agonist ligands. This method is fast and is scalable for high-throughput screening of drugs targeting protein-protein interactions.

Indexed as

FluorescenceProtein MultimerizationErbB ReceptorsHumansImage Processing, Computer-AssistedLigandsMicroscopy, ConfocalProtein BindingProtein Interaction Domains and MotifsReceptors, Gastrointestinal HormoneReceptors, G-Protein-CoupledSignal TransductionSpectrometry, FluorescenceEGFR protein, humanErbB ReceptorsLigandsReceptors, Gastrointestinal HormoneReceptors, G-Protein-Coupledsecretin receptor

Identifiers

PMID31110281
PMCPMC7617210

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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.