National Institutes of Health/National Institute Of Allergy and Infectious Diseases (NIH/NIAID)
AI089728
United States
National Institutes of Health/National Institute Of Allergy and Infectious Diseases (NIH/NIAID)
AI110700
United States
National Institutes of Health/National Institute Of Allergy and Infectious Diseases (NIH/NIAID)
AI171954
United States
Citation
Journal: PLoS Pathog / Year: 2024 Title: Structure-guided in vitro evolution of nanobodies targeting new viral variants. Authors: Gang Ye / Fan Bu / Ruangang Pan / Alise Mendoza / Ge Yang / Benjamin Spiller / Brian E Wadzinski / Lanying Du / Stanley Perlman / Bin Liu / Fang Li / Abstract: A major challenge in antiviral antibody therapy is keeping up with the rapid evolution of viruses. Our research shows that nanobodies - single-domain antibodies derived from camelids - can be rapidly ...A major challenge in antiviral antibody therapy is keeping up with the rapid evolution of viruses. Our research shows that nanobodies - single-domain antibodies derived from camelids - can be rapidly re-engineered to combat new viral strains through structure-guided in vitro evolution. Specifically, for viral mutations occurring at nanobody-binding sites, we introduce randomized amino acid sequences into nanobody residues near these mutations. We then select nanobody variants that effectively bind to the mutated viral target from a phage display library. As a proof of concept, we used this approach to adapt Nanosota-3, a nanobody originally identified to target the receptor-binding domain (RBD) of early Omicron subvariants, making it highly effective against recent Omicron subvariants. Remarkably, this adaptation process can be completed in less than two weeks, allowing drug development to keep pace with viral evolution and provide timely protection to humans.
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