Development of a new genotype–phenotype linked antibody screening system

Antibodies are powerful tools for the therapy and diagnosis of various diseases. In addition to conventional hybridoma-based screening, recombinant antibody-based screening has become a common choice; however, its application is hampered by two factors: (1) screening starts after Ig gene cloning and recombinant antibody production only, and (2) the antibody is composed of paired chains, heavy and light, commonly expressed by two independent expression vectors. Here, we introduce a method for the rapid screening of recombinant monoclonal antibodies by establishing a Golden Gate-based dual-expression vector and in-vivo expression of membrane-bound antibodies. Using this system, we demonstrate the rapid isolation of influenza cross-reactive antibodies with high affinity from immunized mice within 7 days. This system is particularly useful for isolating therapeutic or diagnostic antibodies, for example during foreseen pandemics.

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Publication Details

Journal
eLife
Published
2024-11-19
DOI
https://doi.org/10.7554/elife.95346.3
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Development of a new genotype–phenotype linked antibody screening system

Naveen Kumar, Takashi Watanabe, Yoshiki Mochizuki, Tomohiro Kurosaki et al.
eLife
Monoclonal and Polyclonal Antibodies Research
article

Development of a new genotype–phenotype linked antibody screening system

Naveen Kumar, Takashi Watanabe, Yoshiki Mochizuki, Tomohiro Kurosaki, Fumie Yokoyama, Hidehiro Fukuyama, Osamu Ohara, Tomoko Hasegawa, Hikaru Hata
article en

Abstract

Antibodies are powerful tools for the therapy and diagnosis of various diseases. In addition to conventional hybridoma-based screening, recombinant antibody-based screening has become a common choice; however, its application is hampered by two factors: (1) screening starts after Ig gene cloning and recombinant antibody production only, and (2) the antibody is composed of paired chains, heavy and light, commonly expressed by two independent expression vectors. Here, we introduce a method for the rapid screening of recombinant monoclonal antibodies by establishing a Golden Gate-based dual-expression vector and in-vivo expression of membrane-bound antibodies. Using this system, we demonstrate the rapid isolation of influenza cross-reactive antibodies with high affinity from immunized mice within 7 days. This system is particularly useful for isolating therapeutic or diagnostic antibodies, for example during foreseen pandemics.

eLifeVol. 13
Kansai Medical University (JP), Inserm (FR), Kazusa DNA Research Institute (JP), RIKEN Center for Integrative Medical Sciences (JP), Genomics (United Kingdom) (GB), The University of Osaka (JP)
Japan Society for the Promotion of Science, RIKEN
Good health and well-being
Openalex Percentile: Top 66%
Monoclonal and Polyclonal Antibodies Research
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