Evidence map›Paper›PMID 23580666›Full record

ArticleJournal of biomolecular screening2013

A multiplexed fluorescent assay for independent second-messenger systems: decoding GPCR activation in living cells.

Paul H Tewson, Anne Marie Quinn, Thomas E Hughes

Open access · hybridAbstract read
In one paragraph

Article in Journal of biomolecular screening, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Regulation of Diacylglycerol Content in Olfactory Neurons Determines Forgetting or Retrieval of Olfactory Memory inThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Diacylglycerol kinases regulate TRPV1 channel activity.The Journal of biological chemistry · 2020
    Article
  8. Review
  9. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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 2 institutions in 1 country.

Paul H TewsonMontana Molecular, Bozeman, MT 59717, USA.
Anne Marie Quinn
Thomas E Hughes
Montana Molecular (United States) · USMontana State University · US

Funding

Fast and Accurate Tools for Measuring Fluorescence in Living CellsR44NS082222 · NINDS · MONTANA MOLECULAR, LLC · PI HUGHES, THOMAS E, QUINN, ANNE MARIE · 2014 to 2018
$1.6M
Fast and Accurate Tools for Measuring Fluorescence in Living CellsR43MH096670 · NIMH · MONTANA MOLECULAR, LLC · PI GILLISPIE, GREGORY DAVID, HUGHES, THOMAS E · 2011 to 2011
$348k
NIMH NIH HHS 1R43MH096670- 01A1NIMH NIH HHS R43 MH096670NINDS NIH HHS R44 NS082222
6 · The paper itself

Abstract

There is a growing need in drug discovery and basic research to measure multiple second-messenger components of cell signaling pathways in real time and in relevant tissues and cell types. Many G-protein-coupled receptors activate the heterotrimeric protein, Gq, which in turn activates phospholipase C (PLC). PLC cleaves phosphatidylinositol 4,5-bisphosphate (PIP2) to produce two second messengers: diacylglycerol (DAG), which remains in the plasma membrane, and inositol triphosphate (IP3), which diffuses through the cytosol to release stores of intracellular calcium ions (Ca(2+)). Our goal was to create a series of multiplex sensors that would make it possible to simultaneously measure two different components of the Gq pathway in living cells. Here we describe new fluorescent sensors for DAG and PIP2 that produce robust changes in green or red fluorescence and can be combined with one another, or with existing Ca(2+) sensors, in a live-cell assay. These assays can detect multiple components of Gq signaling, simultaneously in real time, on standard fluorescent plate readers or live-cell imaging systems.

Indexed as

Biological AssayCalcium SignalingAdenosine TriphosphateBiosensing TechniquesDiglyceridesGreen Fluorescent ProteinsHEK293 CellsHumansLuminescent ProteinsPhosphatidylinositol 4,5-DiphosphateProtein Kinase C-deltaReceptors, G-Protein-CoupledRecombinant Fusion ProteinsRed Fluorescent ProteinSecond Messenger SystemsSpectrometry, FluorescenceAdenosine TriphosphateDiglyceridesGreen Fluorescent ProteinsLuminescent ProteinsPhosphatidylinositol 4,5-DiphosphateProtein Kinase C-deltaReceptors, G-Protein-CoupledRecombinant Fusion ProteinsRed Fluorescent ProteinType C Phospholipasescell-based assaysfluorescence methodsG-protein–coupled receptors (GPCR)multiplex assays and technology

Identifiers

PMID23580666
PMCPMC4242713
OpenAlexW2114429916

What OpenQuestion holds

Textmetadata
LicenceTDM
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.