2010Zhongguo shengwu gongcheng zazhiRequires access

Construct and Characterization of Human Nave ScFv Phage Display Library

Zhao Hong

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Abstract

Phage display antibody library is an important technology for generating therapeutic antibody.It was reported that the construction and characterization of a large human antibody phage display library.Total RNA was extracted from peripheral blood lymphocytes of 20 healthy donors.VH and VL gene were amplified by RT-PCR.The ScFv(single chain variable fragment)gene were assembled by overlap PCR,and cloned into a phagemid vector by electroporation of E.coli TG1.A large nave human ScFv phage antibody library containing 1.3×109 antibody members was constructed by repetitive electroporation about 300 times.The quality of the library was examined by sequence analysis and selection against 5 different protein antigens.Sequence analysis of the randomly picked 40 clones showed this library had good diversity.Panning of the 5 different antigens all resulted in successful isolation of antigen specific ScFv antibodies.The results indicate that a large nave human ScFv phage antibody library with good diversity was constructed successfully.

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What this paper is about

Phage display antibody library is an important technology for generating therapeutic antibody.It was reported that the construction and characterization of a large human antibody phage display library.Total RNA was extracted from peripheral blood lymphocytes of 20 healthy donors.VH and VL gene were amplified by RT-PCR.The ScFv(single chain variable fragment)gene were assembled by overlap PCR,and cloned into a phagemid vector by electroporation of E.coli TG1.A large nave human ScFv phage antibody library containing 1.3×109 antibody members was constructed by repetitive electroporation about 300 times.The quality of the library was examined by sequence analysis and selection against 5 different protein antigens.Sequence analysis of the randomly picked 40 clones showed this library had good diversity.Panning of the 5 different antigens all resulted in successful isolation of antigen specific ScFv antibodies.The results indicate that a large nave human ScFv phage antibody library with good diversity was constructed successfully.

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Available abstract

Phage display antibody library is an important technology for generating therapeutic antibody.It was reported that the construction and characterization of a large human antibody phage display library.Total RNA was extracted from peripheral blood lymphocytes of 20 healthy donors.VH and VL gene were amplified by RT-PCR.The ScFv(single chain variable fragment)gene were assembled by overlap PCR,and cloned into a phagemid vector by electroporation of E.coli TG1.A large nave human ScFv phage antibody library containing 1.3×109 antibody members was constructed by repetitive electroporation about 300 times.The quality of the library was examined by sequence analysis and selection against 5 different protein antigens.Sequence analysis of the randomly picked 40 clones showed this library had good diversity.Panning of the 5 different antigens all resulted in successful isolation of antigen specific ScFv antibodies.The results indicate that a large nave human ScFv phage antibody library with good diversity was constructed successfully.

Key concepts: Phage display, Panning (audio), Phagemid, Antibody, Single-chain variable fragment, Electroporation, Antigen, Molecular biology

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