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通过双水相萃取与亲和沉淀集成来纯化重组蛋白 A。

Purification of recombinant protein A by aqueous two-phase extraction integrated with affinity precipitation.

机构信息

Department of Biotechnology, Chemical Center, University of Lund, Lund, Sweden.

出版信息

Biotechnol Bioeng. 1992 Dec 20;40(11):1381-7. doi: 10.1002/bit.260401112.

Abstract

Aqueous two-phase extraction incorporated affinity precipitation was examined as a technique for protein purification. An enteric coating polymer, Eudragit S100, was employed as a ligand carrier. Eudragit was specifically partitioned to the top phase in the aqueous two-phase systems. For application of this method to purification of recombinant protein A using human IgG coupled to Eudragit in an aqueous two-phase system, 80% of protein A added was recovered with 81% purity. The purity was enhanced 26-fold by third method. The IgG-Eudragit could be used repeatedly for the purification process. This seperation method should be applicable to industrial-scale purification as a new purification procedure combining the advantages and compensating for the disadvantages of the aqueous two-phase method and affinity precipitation method.

摘要

水相双相萃取结合亲和沉淀被视为一种蛋白质纯化技术。肠溶性聚合物 Eudragit S100 被用作配体载体。Eudragit 专门分配到水相双相系统的上相中。为了将这种方法应用于使用与人 IgG 偶联的 Eudragit 在水相双相系统中纯化重组蛋白 A,加入的 80%的蛋白 A 被回收,纯度为 81%。通过第三种方法,纯度提高了 26 倍。IgG-Eudragit 可重复用于纯化过程。这种分离方法可以作为一种新的纯化程序,结合水相双相法和亲和沉淀法的优点并弥补其缺点,适用于工业规模的纯化。

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