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A fine-tuned yeast surface-display/secretion platform enables the rapid discovery of neutralizing antibodies against Clostridioides difficile toxins.
Sun, Ying; Zhang, Yongrong; Yu, Hua; Saint Fleur, Ashley; Yu, Di; Yang, Zhiyong; Feng, Hanping.
  • Sun Y; Department of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, MD, 21201, USA. suny@cmu.edu.cn.
  • Zhang Y; Department of Pathogen Biology, School of Basic Medical Sciences, China Medical University, Shenyang, 110122, China. suny@cmu.edu.cn.
  • Yu H; Department of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, MD, 21201, USA.
  • Saint Fleur A; Fzata, Inc, Halethorpe, MD, 21227, USA.
  • Yu D; Department of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, MD, 21201, USA.
  • Yang Z; Department of Microbial Pathogenesis, School of Dentistry, University of Maryland, Baltimore, MD, 21201, USA.
  • Feng H; Fzata, Inc, Halethorpe, MD, 21227, USA.
Microb Cell Fact ; 22(1): 194, 2023 Sep 25.
Article en En | MEDLINE | ID: mdl-37749574
ABSTRACT

BACKGROUND:

Neutralizing antibody plays a key role in protecting hosts from invasive pathogens and their virulent components. Current high-throughput assays for antibody screening are based on binding activities. However, those antibodies with high affinity may not have neutralizing activities. Subsequent functionality assays are necessary to identify neutralizing antibodies from binders with high affinity to their target antigens, which is laborious and time-consuming. Therefore, a versatile platform that can rapidly identify antibodies with both high binding affinity and neutralizing activity is desired to curb future pandemics like COVID-19.

RESULTS:

In this proof-of-concept study, we adapted Saccharomyces cerevisiae to either display human antibodies on the yeast surface or secrete soluble antibodies into the cultivation supernatant under a controllable 'switch' through different carbon source induced promoters. Initially, an engineered chimeric-bispecific Fab antibody, derived from humanized nanobodies against both Clostridioides difficile toxin A and B (TcdA and TcdB), was successfully expressed either on the yeast cell surface or in the culture medium with intact bioactivity, suggesting the applicability of our system in antibody display and secretion. Next, a combinatorial Fab library was constructed from B cells isolated from a convalescent patient with a high serological neutralizing titer against TcdB. Following three rounds of magnetic bead enrichment and one round of flow cytometry sorting, antibodies against TcdB were enriched efficiently. We then sorted out single binders with high binding affinity and induced them to express soluble antibodies in culture medium. The neutralizing activity of culture supernatant was analyzed using cell-based assay immediately. This way, we rapidly identified two unique neutralizers (out of seven binders) that can neutralize the cytotoxicity of TcdB.

CONCLUSION:

The antibody screening platform described here simplifies the neutralizing antibody discovery procedure and will be an attractive alternative for screening functional antibodies against infectious diseases.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Toxinas Bacterianas / Clostridioides difficile / COVID-19 Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Toxinas Bacterianas / Clostridioides difficile / COVID-19 Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article