Affinity purification of yeast cytochrome oxidase with biotinylated subunits 4, 5, or 6

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Abstract

Null mutants in COX4, COX5a, or COX6, which encode subunits 4, 5, and 6 of yeast cytochrome oxidase are blocked in assembly of the enzyme. The mutants are complemented by gene constructs expressing cytochrome oxidase subunits with a carboxyl terminal extension containing a biotinylation signal sequence. Spectra and enzyme activities of mitochondria from transformants expressing a biotinylated subunit indicate restoration of a functional cytochrome oxidase. Biotinylated cytochrome oxidase can be affinity-purified from mitochondrial extracts by fractionation on a monomeric avidin column. This method can be used to purify the enzyme from small amounts of starting material.

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Glerum, D. M., & Tzagoloff, A. (1998). Affinity purification of yeast cytochrome oxidase with biotinylated subunits 4, 5, or 6. Analytical Biochemistry, 260(1), 38–43. https://doi.org/10.1006/abio.1998.2683

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