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Visualizing VDAC1 in live cells using a tetracysteine tag

The voltage-dependent anion channel 1 (VDAC1) is a crucial gatekeeper in the outer mitochondrial membrane, controlling metabolic and energy homeostasis. The available methodological approaches fell short of accurate visualization of VDAC1 in living cells. To permit precise VDAC1 imaging, we utilized...

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Published in:PloS one 2024-10, Vol.19 (10), p.e0311107
Main Authors: Pilic, Johannes, Oflaz, Furkan E, Gottschalk, Benjamin, Erdogan, Yusuf C, Graier, Wolfgang F, Malli, Roland
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Oflaz, Furkan E
Gottschalk, Benjamin
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Graier, Wolfgang F
Malli, Roland
description The voltage-dependent anion channel 1 (VDAC1) is a crucial gatekeeper in the outer mitochondrial membrane, controlling metabolic and energy homeostasis. The available methodological approaches fell short of accurate visualization of VDAC1 in living cells. To permit precise VDAC1 imaging, we utilized the tetracysteine (TC)-tag and visualized VDAC1 dynamics in living cells. TC-tagged VDAC1 had a cluster-like distribution on mitochondria. The labeling of TC-tagged VDAC1 was validated with immunofluorescence. The majority of VDAC1-TC-clusters were localized at endoplasmic reticulum (ER)-mitochondria contact sites. Notably, VDAC1 colocalized with BCL-2 Antagonist/Killer (BAK)-clusters upon apoptotic stimulation. Using this new tool, we were able to observe VDAC1-TC at mitochondrial fission sites. These findings highlight the suitability of the TC-tag for live-cell imaging of VDAC1, shedding light on the roles of VDAC1 in cellular processes.
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subjects Antibodies
Apoptosis
Bcl-2 protein
Cell culture
Cells
Cells (biology)
Clusters
Cysteine
Cysteine - metabolism
Endoplasmic reticulum
Endoplasmic Reticulum - metabolism
Energy balance
Glucose
HeLa Cells
Homeostasis
Humans
Imaging systems
Immunofluorescence
Ion channels
Lasers
Localization
Methods
Mitochondria
Mitochondria - metabolism
Mitochondrial Dynamics
Morphology
Penicillin
Physiological aspects
Proteins
Voltage-Dependent Anion Channel 1 - metabolism
title Visualizing VDAC1 in live cells using a tetracysteine tag
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