Rapid generation of potent antibodies by autonomous hypermutation in yeast

Nat Chem Biol. 2021 Oct;17(10):1057-1064. doi: 10.1038/s41589-021-00832-4. Epub 2021 Jun 24.

Abstract

The predominant approach for antibody generation remains animal immunization, which can yield exceptionally selective and potent antibody clones owing to the powerful evolutionary process of somatic hypermutation. However, animal immunization is inherently slow, not always accessible and poorly compatible with many antigens. Here, we describe 'autonomous hypermutation yeast surface display' (AHEAD), a synthetic recombinant antibody generation technology that imitates somatic hypermutation inside engineered yeast. By encoding antibody fragments on an error-prone orthogonal DNA replication system, surface-displayed antibody repertoires continuously mutate through simple cycles of yeast culturing and enrichment for antigen binding to produce high-affinity clones in as little as two weeks. We applied AHEAD to generate potent nanobodies against the SARS-CoV-2 S glycoprotein, a G-protein-coupled receptor and other targets, offering a template for streamlined antibody generation at large.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / immunology
  • Antibody Formation / immunology*
  • Antigens
  • COVID-19 / immunology
  • Humans
  • Peptide Library
  • Protein Engineering / methods*
  • Recombinant Proteins / biosynthesis*
  • Recombinant Proteins / metabolism
  • SARS-CoV-2 / immunology
  • SARS-CoV-2 / pathogenicity
  • Saccharomyces cerevisiae / metabolism
  • Single-Domain Antibodies / genetics
  • Single-Domain Antibodies / metabolism
  • Spike Glycoprotein, Coronavirus / immunology

Substances

  • Antibodies
  • Antigens
  • Peptide Library
  • Recombinant Proteins
  • Single-Domain Antibodies
  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2