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白蛋白对在汽巴蓝亲和色谱中酶的结合及回收率的影响。

Effect of albumin on binding and recovery of enzymes in affinity chromatography on Cibacron Blue.

作者信息

Ramadoss C S, Steczko J, Uhlig J W, Axelrod B

出版信息

Anal Biochem. 1983 Apr 15;130(2):481-4. doi: 10.1016/0003-2697(83)90620-6.

Abstract

Bovine serum albumin appears to improve the specificity of Cibacron Blue F3GA in affinity chromatography of enzymes which interact with nucleotides. The action of bovine serum albumin may rest in its ability to selectively mask affinity sites in the dye, which are not specific for the nucleotide-binding region of the enzyme, while not seriously impairing binding nor its elution by nucleotides. Thus, the elution of Chlorella nitrate reductase from a Blue Sepharose chromatographic column by its coenzyme, NADH, fails, unless the column is first treated with bovine serum albumin. Such treatment also improves the recovery of some other nucleotide-binding enzymes tested.

摘要

在与核苷酸相互作用的酶的亲和色谱中,牛血清白蛋白似乎能提高Cibacron Blue F3GA的特异性。牛血清白蛋白的作用可能在于其选择性掩盖染料中对酶的核苷酸结合区域无特异性的亲和位点的能力,同时又不会严重损害结合以及核苷酸对其的洗脱作用。因此,除非先用牛血清白蛋白处理,否则辅酶NADH无法从蓝色琼脂糖色谱柱上洗脱小球藻硝酸还原酶。这种处理也提高了所测试的其他一些核苷酸结合酶的回收率。

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