Construction and diversification of yeast cell surface displayed libraries by yeast mating: application to the affinity maturation of Fab antibody fragments

被引:45
作者
Blaise, L [1 ]
Wehnert, A [1 ]
Steukers, MPG [1 ]
van den Beucken, T [1 ]
Hoogenboom, HR [1 ]
Hufton, SE [1 ]
机构
[1] Dyax SA, B-4000 Liege 1, Belgium
关键词
yeast display; combinatorial Fab library; chain shuffling; selection; antibody mutagenesis; molecular evolution;
D O I
10.1016/j.gene.2004.08.014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Yeast display is a powerful technology for the affinity maturation of human antibody fragments. However, the technology thus far has been limited by the size of antibody libraries that can be generated, as using current transformation protocols libraries of only between 106 and 10(7) are typically possible. We have recently shown that Fab antibodies can be displayed on the cell surface of Saccharomyces cerevisiae [van den Beucken, T., Pieters, H., Steukers, M., van der Vaart, M., Ladner, R.C., Hoogenboom, H.R., Hufton, S.E., 2003. Affinity maturation of Fab antibody fragments by fluorescent-activated cell sorting of yeast-displayed libraries. FEBS Lett. 546, 288-294]. This discovery and the knowledge that Fab antibodies are heterodimeric suggest that independent repertoires of heavy chain (HC) and light chain (LC) can be constructed in haploid yeast strains of opposite mating type. These separate repertoires can then be combined by highly efficient yeast mating. Using this approach, we have rapidly generated a naive human Fab yeast display library of over 10(9) clones. In addition, utilizing error-prone polymerase chain reaction, we have diversified Fab sequences and generated combinatorial and hierarchical chain shuffled libraries with complexities of up to 5 x 10(9) clones. These libraries have been selected for higher affinity using a repeating process of mating-driven chain shuffling and flow cytometric sorting. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:211 / 218
页数:8
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