Massively-multiplexed epitope mapping techniques for viral antigen discovery

• Published in: Frontiers in immunology Vol. 14; p. 1192385
• Main Authors: Hu, Diya, Irving, Aaron T.
• Format: Journal Article
• Language: English
• Published: Frontiers Media S.A 25.09.2023
• Subjects: B cell; epitope; epitope mapping; Immunology; phage-display; T cell
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2023.1192385

Following viral infection, viral antigens bind specifically to receptors on the surface of lymphocytes thereby activating adaptive immunity in the host. An epitope, the smallest structural and functional unit of an antigen, binds specifically to an antibody or antigen receptor, to serve as key sites for the activation of adaptive immunity. The complexity and diverse range of epitopes are essential to study and map for the diagnosis of disease, the design of vaccines and for immunotherapy. Mapping the location of these specific epitopes has become a hot topic in immunology and immune therapy. Recently, epitope mapping techniques have evolved to become multiplexed, with the advent of high-throughput sequencing and techniques such as bacteriophage-display libraries and deep mutational scanning. Here, we briefly introduce the principles, advantages, and disadvantages of the latest epitope mapping techniques with examples for viral antigen discovery.