Generation of a Phage Display Chicken Single-Chain Variable Fragment Library

Phage-displayed antibody fragment libraries can be constructed using essentially any species that is easily immunized, as long as the immunoglobulin variable region gene sequences are known. This protocol describes the procedures for the generation of a phage-displayed chicken single-chain variable fragment (scFv) library after immunization with a target antigen. Briefly, the rearranged heavy chain variable region (<i>V</i> <sub><i>H</i></sub> ) genes and the <i>λ</i> light chain variable region (<i>V</i> <sub><i>λ</i></sub> ) genes are amplified separately and are linked through two separate PCR steps to give the final scFv genes. The genes are then cloned into pComb3XSS to generate the phage display chicken scFv library, which can then be used for test and final library ligations.

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Publication Details

Journal
Cold Spring Harbor Protocols
Published
2024-08-16
DOI
https://doi.org/10.1101/pdb.prot108213
Citations
5
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
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article

Generation of a Phage Display Chicken Single-Chain Variable Fragment Library

Jisu Chae, Junho Chung, Jinsung Noh, Hyori Kim et al.
5 citations
Cold Spring Harbor Protocols
Monoclonal and Polyclonal Antibodies Research
article

Generation of a Phage Display Chicken Single-Chain Variable Fragment Library

Jisu Chae, Junho Chung, Jinsung Noh, Hyori Kim, Hyunji Yang
article en
5 citations

Abstract

Phage-displayed antibody fragment libraries can be constructed using essentially any species that is easily immunized, as long as the immunoglobulin variable region gene sequences are known. This protocol describes the procedures for the generation of a phage-displayed chicken single-chain variable fragment (scFv) library after immunization with a target antigen. Briefly, the rearranged heavy chain variable region (<i>V</i> <sub><i>H</i></sub> ) genes and the <i>λ</i> light chain variable region (<i>V</i> <sub><i>λ</i></sub> ) genes are amplified separately and are linked through two separate PCR steps to give the final scFv genes. The genes are then cloned into pComb3XSS to generate the phage display chicken scFv library, which can then be used for test and final library ligations.

Cold Spring Harbor ProtocolsVol. 2025(8)
Seoul National University (KR), Cancer Research Institute (US), Asan Medical Center (KR)
Monoclonal and Polyclonal Antibodies Research
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