Development of a new genotype–phenotype linked antibody screening system

Author:

Watanabe Takashi1ORCID,Hata Hikaru2,Mochizuki Yoshiki1,Yokoyama Fumie1,Hasegawa Tomoko1,Kumar Naveen3,Kurosaki Tomohiro24,Ohara Osamu15ORCID,Fukuyama Hidehiro267

Affiliation:

1. Laboratory for Integrative Genomics, RIKEN Center for Integrative Medical Sciences

2. Laboratory for Lymphocyte Differentiation, RIKEN Center for Integrative Medical Sciences

3. Laboratory for Integrated Bioinformatics, RIKEN Center for Integrative Medical Sciences

4. Laboratory of Lymphocyte Differentiation, WPI Immunology Frontier Research Center, Osaka University

5. Department of Applied Genomics, Kazusa DNA Research Institute

6. Near-InfraRed Photo-Immunotherapy Research Institute, Kansai Medical University

7. INSERM EST, Strasbourg Cedex 2

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 only after Ig gene cloning and recombinant antibody production, and 2) the antibody is composed of paired chains, heavy and light, commonly expressed from 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 demonstrated the efficient isolation of influenza cross-reactive antibodies with high affinity from mouse germinal center B cells over 4 days. This system is particularly useful for isolating therapeutic or diagnostic antibodies (e.g., during foreseen pandemics).

Publisher

eLife Sciences Publications, Ltd

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