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  • Protocol for the Analysis of Yeast and Human Mitochondrial Respiratory Chain Complexes and Supercomplexes by Blue Native Electrophoresis.

Protocol for the Analysis of Yeast and Human Mitochondrial Respiratory Chain Complexes and Supercomplexes by Blue Native Electrophoresis.

STAR protocols (2020-10-01)
Alba Timón-Gómez, Rafael Pérez-Pérez, Eva Nyvltova, Cristina Ugalde, Flavia Fontanesi, Antoni Barrientos
ABSTRACT

By using negatively charged Coomassie brilliant blue G-250 dye to induce a charge shift on proteins, blue native polyacrylamide gel electrophoresis (BN-PAGE) allows resolution of enzymatically active multiprotein complexes extracted from cellular or subcellular lysates while retaining their native conformation. BN-PAGE was first developed to analyze the size, composition, and relative abundance of the complexes and supercomplexes that form the mitochondrial respiratory chain and OXPHOS system. Here, we present a detailed protocol of BN-PAGE to obtain robust and reproducible results. For complete details on the use and execution of this protocol, please refer to Lobo-Jarne et al. (2018) and Timón-Gómez et al. (2020).

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Trizma® base, Primary Standard and Buffer, ≥99.9% (titration), crystalline
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Cocktail di inibitori delle proteasi, for use with mammalian cell and tissue extracts, DMSO solution
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Soluzione Tripsina-EDTA, 0.25%, sterile-filtered, BioReagent, suitable for cell culture, 2.5 g porcine trypsin and 0.2 g EDTA, 4Na per liter of Hanks′ Balanced Salt Solution with phenol red
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Glicina, ReagentPlus®, ≥99% (HPLC)
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Sodio cloruro, Molecular Biology, DNase, RNase, and protease, none detected, ≥99% (titration)
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BIS-TRIS, ≥98.0% (titration)
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Uridine, powder, BioReagent, suitable for cell culture
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Citocromo c, ≥95% based on Mol. Wt. 12,327 basis, powder, suitable for mammalian cell culture
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6-Aminocaproic acid, ≥99% (titration), powder
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