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Rapid discovery of monoclonal antibodies by microfluidics-enabled FACS of single pathogen-specific antibody-secreting cells.
Fischer, Katrin; Lulla, Aleksei; So, Tsz Y; Pereyra-Gerber, Pehuén; Raybould, Matthew I J; Kohler, Timo N; Yam-Puc, Juan Carlos; Kaminski, Tomasz S; Hughes, Robert; Pyeatt, Gwendolyn L; Leiss-Maier, Florian; Brear, Paul; Matheson, Nicholas J; Deane, Charlotte M; Hyvönen, Marko; Thaventhiran, James E D; Hollfelder, Florian.
Affiliation
  • Fischer K; Department of Biochemistry, University of Cambridge, Cambridge, UK.
  • Lulla A; Department of Biochemistry, University of Cambridge, Cambridge, UK.
  • So TY; MRC Toxicology Unit, Gleeson Building, Cambridge, UK.
  • Pereyra-Gerber P; Cambridge Institute for Therapeutic Immunology and Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, UK.
  • Raybould MIJ; Oxford Protein Informatics Group, Department of Statistics, University of Oxford, Oxford, UK.
  • Kohler TN; Department of Biochemistry, University of Cambridge, Cambridge, UK.
  • Yam-Puc JC; MRC Toxicology Unit, Gleeson Building, Cambridge, UK.
  • Kaminski TS; Department of Biochemistry, University of Cambridge, Cambridge, UK.
  • Hughes R; Department of Molecular Biology, Institute of Biochemistry, Faculty of Biology, University of Warsaw, Warsaw, Poland.
  • Pyeatt GL; MRC Toxicology Unit, Gleeson Building, Cambridge, UK.
  • Leiss-Maier F; Department of Biochemistry, University of Cambridge, Cambridge, UK.
  • Brear P; Department of Biochemistry, University of Cambridge, Cambridge, UK.
  • Matheson NJ; Department of Biochemistry, University of Cambridge, Cambridge, UK.
  • Deane CM; Cambridge Institute for Therapeutic Immunology and Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, UK.
  • Hyvönen M; NHS Blood and Transplant, Cambridge, UK.
  • Thaventhiran JED; Oxford Protein Informatics Group, Department of Statistics, University of Oxford, Oxford, UK.
  • Hollfelder F; Department of Biochemistry, University of Cambridge, Cambridge, UK.
Nat Biotechnol ; 2024 Aug 14.
Article in En | MEDLINE | ID: mdl-39143416
ABSTRACT
Monoclonal antibodies are increasingly used to prevent and treat viral infections and are pivotal in pandemic response efforts. Antibody-secreting cells (ASCs; plasma cells and plasmablasts) are an excellent source of high-affinity antibodies with therapeutic potential. Current methods to study antigen-specific ASCs either have low throughput, require expensive and labor-intensive screening or are technically demanding and therefore not widely accessible. Here we present a straightforward technology for the rapid discovery of monoclonal antibodies from ASCs. Our approach combines microfluidic encapsulation of single cells into an antibody capture hydrogel with antigen bait sorting by conventional flow cytometry. With our technology, we screened millions of mouse and human ASCs and obtained monoclonal antibodies against severe acute respiratory syndrome coronavirus 2 with high affinity (<1 pM) and neutralizing capacity (<100 ng ml-1) in 2 weeks with a high hit rate (>85% of characterized antibodies bound the target). By facilitating access to the underexplored ASC compartment, the approach enables efficient antibody discovery and immunological studies into the generation of protective antibodies.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nat Biotechnol Journal subject: BIOTECNOLOGIA Year: 2024 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nat Biotechnol Journal subject: BIOTECNOLOGIA Year: 2024 Document type: Article Affiliation country: United kingdom