Key result
Affinity selection and deep sequencing of a genomic phage display library successfully mapped multiple norovirus antibody epitopes simultaneously, including the HJT-R3-A9 scFv epitope with a KD of 46 nM.
Why the study?
Human noroviruses exhibit extensive genetic and antigenic diversity that complicates vaccine design, making the identification of additional antibody binding sites associated with virus neutralization of interest.
Affinity selection of a genomic phage display library coupled with deep sequencing provides high-resolution mapping of multiple norovirus epitopes simultaneously from complex samples.
NoV infections are a leading cause of gastroenteritis in the United States. Human NoVs exhibit extensive genetic and antigenic diversity, which makes it challenging to design a vaccine that provides broad protection against infection. Antibodies developed during the immune response play an important role in the control of NoV infections. Neutralizing antibodies that act by sterically blocking the site on the virus used to bind human cells have been identified. Identification of other antibody binding sites associated with virus neutralization is therefore of interest. Here, we use a high-resolution method to map multiple antibody binding sites simultaneously from complex serum samples. The results show that a relatively small number of sites on the virus bind a large number of independently generated antibodies, suggesting that immunodominance plays a role in the humoral immune response to NoV infections.
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Huang et al. (2020) studied Norovirus infection. Genomic phage display library selections and deep sequencing was evaluated on Epitope mapping. Affinity selection and deep sequencing of a genomic phage display library successfully mapped multiple norovirus antibody epitopes simultaneously, including the HJT-R3-A9 scFv epitope with a KD of 46 nM.
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