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Updated: Mar 30, 2026

Study of Endoplasmic Reticulum and Mitochondria Interactions by In Situ Proximity Ligation Assay in Fixed Cells
Published on: December 10, 2016
Detection of Isolated Mitochondria-Associated ER Membranes Using the Sigma-1 Receptor
Abasha Lewis1, Shang-Yi Tsai1, Tsung-Ping Su2
1Cellular Pathobiology Section, IRP, DHHS, NIDA, NIH, 333 Cassell Drive, Baltimore, MD, 21224, USA.
Abstract:
The interface between the endoplasmic reticulum (ER) and mitochondria referred to as the MAM (mitochondria-associated ER membrane) plays important roles in many physiological functions. A specific marker for this important entity of cellular structure is urgently needed. Thus, we propose in this method chapter that the membrane-bound ER chaperone sigma-1 receptor serves as an ideal marker for the MAM. We describe in detail the preparation and purification of the MAM by using the sigma-1 receptor as the marker and demonstrate the uniqueness of this marker by using a variety of cells, peripheral and neuronal.
Insights
Researchers identified the sigma-1 receptor as a reliable marker for the mitochondria-associated ER membrane (MAM). This discovery aids in isolating and studying this crucial cellular structure involved in vital physiological functions.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- The mitochondria-associated ER membrane (MAM) is a critical cellular structure involved in numerous physiological processes.
- A specific and reliable marker for isolating the MAM is currently lacking.
- Understanding MAM function requires precise methods for its isolation and study.
Purpose of the Study:
- To propose and validate the sigma-1 receptor as a specific marker for the MAM.
- To provide a detailed methodology for MAM preparation and purification using the sigma-1 receptor.
- To demonstrate the broad applicability of the sigma-1 receptor as a MAM marker across different cell types.
Main Methods:
- Utilizing the sigma-1 receptor, a membrane-bound ER chaperone, as a targeting molecule.
- Developing and detailing protocols for the preparation and purification of MAM fractions.
- Employing diverse cell models, including peripheral and neuronal cells, for validation.
Main Results:
- The sigma-1 receptor was successfully employed as a marker for MAM isolation.
- Detailed procedures for MAM preparation and purification were established.
- The efficacy of the sigma-1 receptor as a MAM marker was confirmed in various cellular contexts.
Conclusions:
- The sigma-1 receptor is a highly suitable and unique marker for the MAM.
- This method facilitates the isolation and study of MAMs, advancing research into their physiological roles.
- The proposed marker offers a valuable tool for cell biology and neuroscience research.
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