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Site-directed neutralizing antibodies targeting structural sites on SARS-CoV-2 spike protein. | LitMetric

Site-directed neutralizing antibodies targeting structural sites on SARS-CoV-2 spike protein.

N Biotechnol

Institute for Bioscience and Biotechnology Research, University of Maryland, Rockville, MD 20850, USA; Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD 20742, USA.

Published: May 2024

AI Article Synopsis

  • Epivolve is a cutting-edge technology designed to create antibodies that specifically target certain sites on a pathogen by using modified peptides or proteins as immunogens.* -
  • The technology was tested on the SARS-CoV-2 Receptor Binding Domain, leading to the development of neutralizing antibodies against 13 specific sites that interact with the ACE2 receptor.* -
  • One targeted site (SL13) was selected for more in-depth study, showcasing the ability of Epivolve to generate effective antibodies against both the original virus strain and its Omicron variant.*

Article Abstract

'Epivolve' (epitope evolution) is an innovative paratope-evolving technology using a haptenated peptide or protein immunogen as a means of directing the in vivo immune response to specifically targeted sites at a one amino acid residue resolution. Guided by protein structural analysis, Epivolve technology was tested to develop site-directed neutralizing antibodies (nAbs) in a systematic fashion against the SARS-CoV-2 Receptor Binding Domain (RBD). Thirteen solvent-exposed sites covering the ACE2 receptor-binding interface were targeted. Immunogens composed of each targeted site were used to immunize rabbits in separate cohorts. In vivo site-directed immune responses against all 13 targets were demonstrated by B cell secreted IgG and recombinant IgG testing. One site, SL13 (Y505) which mutates from tyrosine to histidine in the SARS-CoV-2 Omicron variant, was chosen as a proof-of-concept (PoC) model for further functional monoclonal antibody development. Epivolve technology demonstrated the capabilities of generating pan-variant antibodies and nAbs against the SARS-CoV-2 primary strain and the Omicron variant.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10954356PMC
http://dx.doi.org/10.1016/j.nbt.2023.12.004DOI Listing

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