Further improvement of broad specificity hapten recognition with protein engineering

被引:41
作者
Korpimäki, T [1 ]
Rosenberg, J
Virtanen, P
Lamminmäki, U
Tuomola, M
Saviranta, P
机构
[1] Univ Turku, Dept Biotechnol, FIN-20520 Turku, Finland
[2] Univ Turku, Dept Bioorgan Chem, FIN-20520 Turku, Finland
来源
PROTEIN ENGINEERING | 2003年 / 16卷 / 01期
关键词
DNA shuffling; drug residues; group specificity; phage display; sulfonamides;
D O I
10.1093/proeng/gzg010
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
Sulfa-antibiotics (sulfonamides) are widely used in veterinary medicine. Meat and milk from treated animals can be contaminated with sulfa residues. Current sulfonamide assays are unfit for screening of food, because they are either too laborious, insensitive or specific for a few sulfa compounds only. An immunoassay for detection of all sulfas in a single reaction would be useful for screening. Previously we have improved the broad specificity sulfa binding of antibody 27G3 with random mutagenesis and phage display. In order to improve the properties of this antibody further, mutants from the previous study were recombined and more mutations introduced. These new libraries were enriched with phage display and several different mutant antibodies were isolated. The cross-reaction profile of the best mutant was better than that of the wild-type antibody and the mutants of the previous study: it was capable of binding 10 of the tested 13 sulfonamides within a narrow concentration range and also bound the rest of the sulfas 5- to 11-fold better than the mutants of the previous study.
引用
收藏
页码:37 / 46
页数:10
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