Evidence map›Paper›PMID 31701023›Full record

ArticleCommunications biology2019

FRET-based cyclic GMP biosensors measure low cGMP concentrations in cardiomyocytes and neurons.

Gaia Calamera, Dan Li, Andrea Hembre Ulsund, Jeong Joo Kim, Oliver C Neely, Lise Román Moltzau, Marianne Bjørnerem, David Paterson, Choel Kim, Finn Olav Levy and 1 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 41 citations in OpenAlex.

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  16. A Real-Time, Plate-Based BRET Assay for Detection of cGMP in Primary Cells.International journal of molecular sciences · 2022
    Article
  17. Article
  18. Review
  19. Review
  20. CUTie2: The Attack of the Cyclic Nucleotide Sensor Clones.Frontiers in molecular biosciences · 2021
    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

11 authors at 3 institutions in 3 countries.

Gaia Calamera1Department of Pharmacology, Institute of Clinical Medicine, University of Oslo and Oslo University Hospital, Oslo, Norway.
Dan Li3Department of Physiology, Anatomy and Genetics, Oxford University, Oxford, UK.
Andrea Hembre Ulsund1Department of Pharmacology, Institute of Clinical Medicine, University of Oslo and Oslo University Hospital, Oslo, Norway.
Jeong Joo Kim4Department of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX USA.
Oliver C Neely3Department of Physiology, Anatomy and Genetics, Oxford University, Oxford, UK.
Lise Román Moltzau1Department of Pharmacology, Institute of Clinical Medicine, University of Oslo and Oslo University Hospital, Oslo, Norway.
Marianne Bjørnerem1Department of Pharmacology, Institute of Clinical Medicine, University of Oslo and Oslo University Hospital, Oslo, Norway.
David Paterson3Department of Physiology, Anatomy and Genetics, Oxford University, Oxford, UK.ORCID 0000-0002-7399-3256
Choel Kim4Department of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX USA.
Finn Olav Levy1Department of Pharmacology, Institute of Clinical Medicine, University of Oslo and Oslo University Hospital, Oslo, Norway.
Kjetil Wessel Andressen1Department of Pharmacology, Institute of Clinical Medicine, University of Oslo and Oslo University Hospital, Oslo, Norway.ORCID 0000-0003-1094-1501
Oslo University Hospital · NOUniversity of Oxford · GBBaylor College of Medicine · US

Funding

Targeting mechanisms of cGMP dependent protein kinases by peptide arrays and crysR01GM090161 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI KIM, CHOEL WOONG · 2010 to 2018
$2.9M
NIGMS NIH HHS R01 GM090161
6 · The paper itself

Abstract

Several FRET (fluorescence resonance energy transfer)-based biosensors for intracellular detection of cyclic nucleotides have been designed in the past decade. However, few such biosensors are available for cGMP, and even fewer that detect low nanomolar cGMP concentrations. Our aim was to develop a FRET-based cGMP biosensor with high affinity for cGMP as a tool for intracellular signaling studies. We used the carboxyl-terminal cyclic nucleotide binding domain of

Indexed as

AnimalsBiosensing TechniquesComputer SystemsCyclic GMPCyclic GMP-Dependent Protein KinasesFluorescence Resonance Energy TransferGuanylate CyclaseHEK293 CellsHumansMaleModels, MolecularMyocytes, CardiacNeuronsPlasmodium falciparumProtozoan ProteinsRats, WistarCyclic GMPCyclic GMP-Dependent Protein KinasesGuanylate CyclaseProtozoan ProteinsRecombinant Fusion ProteinsSoluble Guanylyl CyclaseCell signallingCellular imagingFluorescent proteinsMembrane proteins

Identifiers

PMID31701023
PMCPMC6820734
OpenAlexW2982341276

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.