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 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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Journal
PLoS ONE
Published
2024-10-18
DOI
https://doi.org/10.1371/journal.pone.0311107
Citations
1
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
0.23

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article

Visualizing VDAC1 in live cells using a tetracysteine tag

Yusuf C. Erdoğan, Johannes Pilic, Wolfgang F. Graier, Furkan Enes Oflaz et al.
1 citations
PLoS ONE
Mitochondrial Function and Pathology
0.23
article

Visualizing VDAC1 in live cells using a tetracysteine tag

Yusuf C. Erdoğan, Johannes Pilic, Wolfgang F. Graier, Furkan Enes Oflaz, Benjamin Gottschalk, Roland Malli
article en
1 citations

Abstract

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.

PLoS ONEVol. 19(10)
Medical University of Graz (AT), BioTechMed-Graz (AT)
Austrian Science Fund, Karl-Franzens-Universität Graz, Medizinische Universität Graz
Affordable and clean energy
Openalex Percentile: Top 42%
Mitochondrial Function and Pathology
0.23
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