Summary: T cells play a critical role in cellular immune responses to pathogens and cancer and can be activated and expanded by Major Histocompatibility Complex (MHC)-presented antigens contained in peptide vaccines. We present a machine learning method to optimize the presentation of peptides by class II MHCs by modifying their anchor residues. Our method first learns a model of peptide affinity for a class II MHC using an ensemble of deep residual networks, and then uses the model to propose anchor residue changes to improve peptide affinity. We use a high throughput yeast display assay to show that anchor residue optimization improves peptide binding.
Supplementary Information: Supplementary data are available at Bioinformatics online.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8504626 | PMC |
http://dx.doi.org/10.1093/bioinformatics/btab131 | DOI Listing |
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