噬菌体展示
重组DNA
选择(遗传算法)
抗体
化学
分子生物学
噬菌体
蛋白质工程
计算生物学
变性(裂变材料)
生物
生物化学
噬菌体
遗传学
计算机科学
基因
大肠杆菌
酶
人工智能
核化学
作者
Eeva‐Christine Brockmann
出处
期刊:Methods in molecular biology
日期:2012-01-01
卷期号:: 123-144
被引量:7
标识
DOI:10.1007/978-1-61779-974-7_7
摘要
ScFv fragments are popular recombinant antibody formats but often suffer from limited stability. Phage display is a powerful tool in antibody engineering and applicable also for stability selection. ScFv variants with improved stability can be selected from large randomly mutated phage displayed libraries with a specific antigen after the unstable variants have been inactivated by heat or GdmCl. Irreversible scFv denaturation, which is a prerequisite for efficient selection, is achieved by combining denaturation with reduction of the intradomain disulfide bonds. Repeated selection cycles of increasing stringency result in enrichment of stabilized scFv fragments. Procedures for constructing a randomly mutated scFv library by error-prone PCR and phage display selection for enrichment of stable scFv antibodies from the library are described here.
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