Affinity ligands for industrial protein purification

被引:26
作者
Linhult, M [1 ]
Gülich, S
Hober, S
机构
[1] Albanova Univ Ctr, Dept Biotechnol, Royal Inst Technol, SE-10691 Stockholm, Sweden
[2] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
关键词
Affinity chromatography; cleaning-in-place (CIP); deamidation; protein A; protein G; protein engineering; stabilization;
D O I
10.2174/0929866053765662
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Significant efforts are put into the design of large-scale purification processes of proteins due to great demands regarding cost efficiency and safety. In order to design an effective purification scheme the unit operations need to be reduced to a minimum. In this review we are discussing proteinaceous ligands as well as small synthetic mimics for use in affinity chromatography for large-scale applications. Different advantages as well as drawbacks of the two approaches are outlined.
引用
收藏
页码:305 / 310
页数:6
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