Protocol for the in vivo quantification of mitochondria-associated ER membranes in Caenorhabditis elegans

<h2>Summary</h2> Mitochondria-associated membranes (MAMs) are specialized contact sites between the endoplasmic reticulum and mitochondria, with multiple functional aspects. Here, we present a confocal microscopy-based protocol for quantifying the area of MAM-like domains in intestinal cells of the nematode <i>Caenorhabditis elegans</i> using organelle-specific fluorescent reporters. We describe steps for worm synchronization, microscope setup, sample preparation, and image acquisition. We then detail procedures for manual single-image analysis and scalable automated batch processing, enabling robust quantification of ER-mitochondria contacts across experimental conditions. For complete details on the use and execution of this protocol, please refer to Roussos et al.<sup>1</sup>

Authors

Institutions

Publication Details

Journal
STAR Protocols
Published
2026-05-22
DOI
https://doi.org/10.1016/j.xpro.2026.104592
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Protocol for the in vivo quantification of mitochondria-associated ER membranes in Caenorhabditis elegans

Konstantinos Palikaras, Fivos Borbolis
STAR Protocols
Mitochondrial Function and Pathology
article

Protocol for the in vivo quantification of mitochondria-associated ER membranes in Caenorhabditis elegans

Konstantinos Palikaras, Fivos Borbolis
article en

Abstract

<h2>Summary</h2> Mitochondria-associated membranes (MAMs) are specialized contact sites between the endoplasmic reticulum and mitochondria, with multiple functional aspects. Here, we present a confocal microscopy-based protocol for quantifying the area of MAM-like domains in intestinal cells of the nematode <i>Caenorhabditis elegans</i> using organelle-specific fluorescent reporters. We describe steps for worm synchronization, microscope setup, sample preparation, and image acquisition. We then detail procedures for manual single-image analysis and scalable automated batch processing, enabling robust quantification of ER-mitochondria contacts across experimental conditions. For complete details on the use and execution of this protocol, please refer to Roussos et al.<sup>1</sup>

STAR ProtocolsVol. 7(2)
University of Patras (GR), National and Kapodistrian University of Athens (GR)
European Research Council
Zero hunger
Openalex Percentile: Top 8%
Mitochondrial Function and Pathology
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.