An improved phage display vector for antibody repertoire cloning by construction of combinatorial libraries

被引:9
|
作者
Burioni, R
Plaisant, P
DelliCarri, V
Vannini, A
Spanu, T
Clementi, M
Fadda, G
Varaldo, PE
机构
[1] UNIV TRIESTE, DIPARTIMENTO SCI BIOMED, I-34100 TRIESTE, ITALY
[2] UNIV ANCONA, IST MICROBIOL, I-60100 ANCONA, ITALY
来源
RESEARCH IN VIROLOGY | 1997年 / 148卷 / 02期
关键词
cloning vector; phage display; combinatorial library; human monoclonal; antibody; recombinant antibodies; repertoire cloning; bacterial acid phosphatase gene;
D O I
10.1016/S0923-2516(97)89903-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Phagemid pComb3 is a widely used vector for molecular cloning of the antibody repertoire and for production of phage display libraries. However, in practical use, the utilization of this vector has some drawbacks. In this work we describe the construction of pComb3/TIG, an improved, easily manipulated vector for the cloning and display of antibody fragment libraries on the surface of filamentous phage. The two small ''stuffer'' fragments at the cloning sites were replaced with long DNA fragments, for easier differentiation of the correctly cut forms of the vector. Moreover, in pComb3/TIG the fragment at the heavy-chain-fragment cloning site contains an acid phosphatase-encoding gene. This feature allows the easy distinction of the Escherichia coli cells containing the unmodified form of the phagemid instead of the heavy-chain fragment coding cDNA in a simple plate histochemical assay.
引用
收藏
页码:161 / 164
页数:4
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