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蛋白质纯化的新方法。置换色谱法。

New methods of protein purification. Displacement chromatography.

作者信息

Galaev I Y

机构信息

Department of Biotechnology, Center for Chemistry and Chemical Engineering, Lund University, Lund, S-22100, Sweden. biot-iga@hermes. lu.se.

出版信息

Biochemistry (Mosc). 1998 Nov;63(11):1258-65.

PMID:9864463
Abstract

This review discusses a new method for protein purification, displacement chromatography. Elution of proteins bound to an adsorbent is carried out in displacement chromatography by a substance, the so-called "displacer", which has a higher affinity for the chromatographic matrix than any of the adsorbed proteins. The latter are "pushed out" from the matrix by the displacer and form a displacement train when moving along the column. The component with the weakest affinity moves first, and the one with the highest affinity moves last in the train. The concentration of the component in the displacement zone is determined by the intersection of the operating line and binding isotherm of the given component. The shape of the displacement zone is close to rectangular. A more powerful resolving force is created compared to other methods of selective elution, especially at high column loadings, when nearly the whole working capacity of the column is used. Independence of component concentration in the displacement zone on its content in the feed allows significant concentrating of the purified protein during displacement chromatography. Examples of application of displacement chromatography for the separation of model protein systems and purification of proteins from crude extracts are discussed as well as methods of column regeneration.

摘要

本综述讨论了一种蛋白质纯化的新方法——置换色谱法。在置换色谱法中,通过一种对色谱基质的亲和力高于任何吸附蛋白质的物质(即所谓的“置换剂”)来洗脱与吸附剂结合的蛋白质。后者被置换剂从基质中“推出”,并在沿柱移动时形成一个置换序列。亲和力最弱的组分最先移动,而亲和力最强的组分在序列中最后移动。置换区中组分的浓度由给定组分的操作线和结合等温线的交点决定。置换区的形状接近矩形。与其他选择性洗脱方法相比,置换色谱法产生了更强的分辨力,尤其是在高柱负荷下,此时几乎使用了柱的全部工作容量。置换区中组分浓度与其进料中含量无关,这使得在置换色谱过程中能够对纯化的蛋白质进行显著浓缩。文中讨论了置换色谱法在分离模型蛋白质系统和从粗提物中纯化蛋白质方面的应用实例以及柱再生方法。

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