Evidence map›Paper›PMID 34179249›Full record

ArticleBio-protocol2018

Measuring Mitochondrial ROS in Mammalian Cells with a Genetically Encoded Protein Sensor.

Xin Zhang, Christine Silvia Gibhardt, Sabrina Cappello, Katharina Maria Zimmermann, Adina Vultur, Ivan Bogeski

Open access · greenAbstract read
In one paragraph

Article in Bio-protocol, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 54% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
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

6 authors at 1 institution in 1 country.

Xin ZhangMolecular Physiology, Institute of Cardiovascular Physiology, University Medical Center, University of Göttingen, Göttingen, Germany.
Christine Silvia GibhardtMolecular Physiology, Institute of Cardiovascular Physiology, University Medical Center, University of Göttingen, Göttingen, Germany.
Sabrina CappelloMolecular Physiology, Institute of Cardiovascular Physiology, University Medical Center, University of Göttingen, Göttingen, Germany.
Katharina Maria ZimmermannDepartment of Biophysics, CIPMM, School of Medicine, Saarland University, 66421 Homburg, Germany.
Adina VulturMolecular Physiology, Institute of Cardiovascular Physiology, University Medical Center, University of Göttingen, Göttingen, Germany.
Ivan BogeskiMolecular Physiology, Institute of Cardiovascular Physiology, University Medical Center, University of Göttingen, Göttingen, Germany.
Saarland University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reactive oxygen species (ROS) are not only known for their toxic effects on cells, but they also play an important role as second messengers. As such, they control a variety of cellular functions such as proliferation, metabolism, differentiation and apoptosis. Thus, ROS are involved in the regulation of multiple physiological and pathophysiological processes. It is now apparent that there are transient and local changes in ROS in the cell; in so-called 'microdomains' or in specific cellular compartments, which affect signaling events. These ROS hotspots need to be studied in more depth to understand their function and regulation. Therefore, it is necessary to identify and quantify redox signals in single cells with high spatial and temporal resolution. Genetically encoded fluorescence-based protein sensors provide such necessary tools to examine redox-signaling processes. A big advantage of these sensors is the possibility to target them specifically. Mitochondria are essential for energy metabolism and are one of the major sources of ROS in mammalian cells. Therefore, the evaluation of redox potential and ROS production in these organelles is of great interest. Herein, we provide a protocol for the real-time visualization of mitochondrial hydrogen peroxide (H

Indexed as

Fluorescence microscopyHyPerMammalian cellMitochondrial ROSProtein sensorReal-time imagingroGFP-Orp1

Identifiers

PMID34179249
PMCPMC8203962
OpenAlexW2794251770

What OpenQuestion holds

Textmetadata
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.