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Related Concept Videos

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Hybridoma Technology

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Hybridoma technology is used for the large-scale production of monoclonal antibodies. Monoclonal antibodies bind to only a single antigenic determinant or epitope. Such antibodies are used in research, diagnostics, and disease therapy. The hybridoma technology established in 1975 by Georges Köhler and Cesar Milstein was awarded the Nobel Prize in Medicine in 1984 for revolutionizing research and therapy.
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Commonly used fusion techniques — electroporation,...
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Related Experiment Video

Updated: Jan 14, 2026

Single-cell Screening Method for the Selection and Recovery of Antibodies with Desired Specificities from Enriched Human Memory B Cell Populations
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Enhancing monoclonal antibody diversity by integrating bulk sorting and machine learning.

Daisuke Hisamatsu1, Rion Ozaki1, Akari Ikeda1

  • 1Intractable Disease Research Center, Juntendo University Graduate School of Medicine, Tokyo, Japan.

Biochemistry and Biophysics Reports
|October 27, 2025
PubMed
Summary

A new synthetic chimeric antibody (SynCA) technology enhances antibody discovery by integrating bulk B cell sorting and machine learning. This cost-effective method rapidly generates diverse therapeutic monoclonal antibodies (mAbs) from convalescent sera.

Keywords:
BCR repertoire diversityBulk sortingLow costMachine learningMonoclonal antibody discoveryPrediction

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Area of Science:

  • Immunology
  • Biotechnology
  • Bioinformatics

Background:

  • Therapeutic monoclonal antibody (mAb) engineering aims to improve affinity and activity.
  • Conventional single-cell sorting for mAb discovery is costly and limits analysis.
  • Identifying potent neutralizing antibodies requires diverse human mAb libraries, especially for rapidly mutating viruses like SARS-CoV-2.

Purpose of the Study:

  • To develop a cost-effective and rapid method for generating diverse human mAb libraries.
  • To overcome limitations of single-cell sorting in antibody discovery.
  • To explore the potential of synthetic chimeric antibody (SynCA) technology for therapeutic antibody development.

Main Methods:

  • Developed synthetic chimeric antibody (SynCA) technology integrating bulk sorting of antigen-specific B cells and machine learning.
  • Cloned antibody variable regions from a single cDNA extracted from approximately 5000 B cells.
  • Compared SynCA method with single-cell sorting using convalescent sera from COVID-19 patients.

Main Results:

  • SynCA method significantly enhanced B cell receptor repertoire diversity in heavy and light chain genes.
  • Random pairing of heavy and light chain genes reconstituted diverse mAbs in vitro.
  • Nucleotide sequence information from antibody gene regions (D H and J L ) was found to predict antibody reconstitution.

Conclusions:

  • SynCA technology offers a cost-effective and rapid alternative for generating diverse mAb libraries.
  • This method facilitates the discovery of therapeutic, diagnostic, and research mAbs.
  • The findings provide new insights into antibody reconstitution prediction based on nucleotide sequence information.