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利用生物素化的亚基4、5或6对酵母细胞色素氧化酶进行亲和纯化。

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

作者信息

Glerum D M, Tzagoloff A

机构信息

Department of Biological Sciences, Columbia University, New York, New York 10027, USA.

出版信息

Anal Biochem. 1998 Jun 15;260(1):38-43. doi: 10.1006/abio.1998.2683.

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.

摘要

COX4、COX5a或COX6的无效突变体(它们编码酵母细胞色素氧化酶的亚基4、5和6)在该酶的组装过程中受阻。这些突变体可被表达带有含生物素化信号序列的羧基末端延伸的细胞色素氧化酶亚基的基因构建体互补。表达生物素化亚基的转化体线粒体的光谱和酶活性表明功能性细胞色素氧化酶得以恢复。生物素化的细胞色素氧化酶可通过在单体抗生物素蛋白柱上分级分离从线粒体提取物中进行亲和纯化。该方法可用于从少量起始材料中纯化该酶。

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