Evidence map›Paper›PMID 36952183›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Proximity-Ligation Assay to Detect Peroxisome-Organelle Interaction.

Maki Kamoshita, Michael Schrader

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

2 authors at 1 institution in 2 countries.

Maki KamoshitaFaculty of Health and Life Sciences, Biosciences, University of Exeter, Exeter, Devon, UK.
Michael SchraderFaculty of Health and Life Sciences, Biosciences, University of Exeter, Exeter, Devon, UK. m.schrader@exeter.ac.uk.
University of Exeter · GB

Funding

Biotechnology and Biological Sciences Research Council BB/R016844/1Biotechnology and Biological Sciences Research Council BB/T002255/1
6 · The paper itself

Abstract

Peroxisomes are essential organelles in mammals, which contribute to cellular lipid metabolism and redox homeostasis. They do not function as isolated entities but cooperate and interact with other subcellular organelles, in particular the endoplasmic reticulum, mitochondria, and lipid droplets. Those interactions are often mediated by membrane contact sites. Tether proteins at those sites bring the organelles in close proximity to facilitate metabolite and lipid transfer as well as organelle communication. There is great interest in the investigation of the physiological functions of peroxisome-organelle contacts and how they are regulated. Here, we present an antibody- and fluorescence-based proximity ligation approach used successfully in our laboratory for the detection and quantification of peroxisome-organelle interactions in cultured mammalian cells.

Indexed as

Endoplasmic ReticulumPeroxisomesAnimalsMammalsMitochondriaMitochondrial MembranesProteinsProteinsCell cultureImmunofluorescenceMembrane contact sitesOrganelle interactionPeroxisomeProximity ligationTransfection

Identifiers

PMID36952183
OpenAlexW4360601059

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.