Abstract:

<p>Major histocompatibility complex (MHC) proteins present peptides on the cell surface for T&nbsp;cell surveillance. Reliable in silico prediction of which peptides would be presented and which T&nbsp;cell receptors would recognize them is an important problem in structural immunology. Here, we introduce an AlphaFold-based pipeline for predicting the three-dimensional structures of peptide-MHC complexes for class I and class II MHC molecules. Our method demonstrates high accuracy, outperforming existing tools in class I modeling accuracy and class II peptide register prediction. We validate its performance and utility with new experimental data on a recently described cancer neoantigen/wild-type peptide pair and explore applications toward improving peptide-MHC binding prediction.</p>