Protocol for the production and reconstitution of VDAC1 for functional assays

The voltage-dependent anion channel (VDAC) is an abundant and multifunctional outer mitochondrial membrane protein, playing key roles in neurodegeneration, apoptosis, and mitochondrial membrane biogenesis. Here, we present a protocol to produce and reconstitute high yields of detergent-solubilized VDAC, expressed as inclusion bodies in E. coli. We describe steps for purification by affinity chromatography and refolding in lauryldimethylamine-N-oxide (LDAO). We then detail procedures for reconstituting VDAC into membrane vesicles to assay its channel and phospholipid scramblase activity via fluorescence-based assays. For complete details on the use and execution of this protocol, please refer to Bergdoll et al.,<sup>1</sup> Queralt-Martín et al., <sup>2</sup> and Jahn et al.<sup>3</sup>.

Authors

Institutions

Publication Details

Journal
STAR Protocols
Published
2024-08-09
DOI
https://doi.org/10.1016/j.xpro.2024.103240
Citations
9
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
Field-Weighted Citation Impact
2.57

Funders

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

Protocol for the production and reconstitution of VDAC1 for functional assays

Ken‐taro Sakata, Lucie Bergdoll, Anant K. Menon, Grace I. Dearden et al.
9 citations
STAR Protocols
Cancer, Hypoxia, and Metabolism
2.57
article

Protocol for the production and reconstitution of VDAC1 for functional assays

Ken‐taro Sakata, Lucie Bergdoll, Anant K. Menon, Grace I. Dearden, Varun Ravishankar
article en
9 citations

Abstract

The voltage-dependent anion channel (VDAC) is an abundant and multifunctional outer mitochondrial membrane protein, playing key roles in neurodegeneration, apoptosis, and mitochondrial membrane biogenesis. Here, we present a protocol to produce and reconstitute high yields of detergent-solubilized VDAC, expressed as inclusion bodies in E. coli. We describe steps for purification by affinity chromatography and refolding in lauryldimethylamine-N-oxide (LDAO). We then detail procedures for reconstituting VDAC into membrane vesicles to assay its channel and phospholipid scramblase activity via fluorescence-based assays. For complete details on the use and execution of this protocol, please refer to Bergdoll et al.,<sup>1</sup> Queralt-Martín et al., <sup>2</sup> and Jahn et al.<sup>3</sup>.

STAR ProtocolsVol. 5(3)
Centre National de la Recherche Scientifique (FR), Cornell University (US), Institut de Microbiologie de la Méditerranée (FR), Délégation Provence et Corse (FR), Architecture et Fonction des Macromolécules Biologiques (FR)
Aix-Marseille Université, Universitat Jaume I, National Institutes of Health
Openalex Percentile: Top 10%
Cancer, Hypoxia, and Metabolism
2.57
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.