Evidence map›Paper›PMID 28004840›Full record

ArticleScientific reports2016

Dual observation of the ATP-evoked small GTPase activation and Ca

Yoshihisa Nakahata, Junichi Nabekura, Hideji Murakoshi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-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

13 citing papers in PubMed, 18 citations in OpenAlex.

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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.

Yoshihisa NakahataDivision of Homeostatic Development, National Institute for Physiological Sciences, Okazaki, Aichi 444-8585, Japan.
Junichi NabekuraDivision of Homeostatic Development, National Institute for Physiological Sciences, Okazaki, Aichi 444-8585, Japan.
Hideji MurakoshiDepartment of Physiological Sciences, The Graduate University for Advanced Studies (SOKENDAI), Okazaki, Aichi 444-8585, Japan.
National Institute for Physiological Sciences · JPThe Graduate University for Advanced Studies, SOKENDAI · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intracellular signal transduction involves a number of biochemical reactions, which largely consist of protein-protein interactions and protein conformational changes. Monitoring Förster resonance energy transfer (FRET) by fluorescence lifetime imaging microscopy (FLIM), called FLIM-FRET, is one of the best ways to visualize such protein dynamics. Here, we attempted to apply dark red fluorescent proteins with significantly smaller quantum yields. Application of the dark mCherry mutants to single-molecule FRET sensors revealed that these dark mCherry mutants are a good acceptor in a pair with mRuby2. Because the FRET measurement between mRuby2 and dark mCherry requires only the red region of wavelengths, it facilitates dual observation with other signaling sensors such as genetically encoded Ca

Indexed as

Adenosine TriphosphateAstrocytesCalciumcdc42 GTP-Binding ProteinFluorescence Resonance Energy TransferGreen Fluorescent ProteinsGTP Phosphohydrolase ActivatorsHeLa CellsHumansLuminescent ProteinsMicroscopy, FluorescenceRed Fluorescent ProteinrhoA GTP-Binding ProteinSignal TransductionSpectrometry, FluorescenceAdenosine TriphosphateCalciumcdc42 GTP-Binding ProteinCDC42 protein, humanGreen Fluorescent ProteinsGTP Phosphohydrolase ActivatorsLuminescent ProteinsRed Fluorescent ProteinrhoA GTP-Binding Protein

Identifiers

PMID28004840
PMCPMC5177924
OpenAlexW2565142838

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.