Structure modeling and specificity of peptide-MHC class I interactions using geometric deep learning

Abstract

Major Histocompatibility Complex (MHC) plays a major role in the adaptive immune response by recognizing foreign proteins through binding to their peptides. In humans alone there are several hundred different MHC alleles, where each allele binds a specific subset of peptides. The peptide-MHC complex on a cell surface is identified by a T-cell receptor (TCR) and this binding invokes an immune response. Therefore, predicting the binding specificity of peptide-MHC pairs is necessary for understanding the immune recognition mechanism. Here, we develop an end-to-end novel deep learning model, MHCfold, that consists of structure and specificity prediction modules for simultaneous modeling of peptide-MHC class I (pMHCI) complexes and prediction of their specificity based on their modeled structure. MHCfold produces highly accurate structures of pMHCI complexes with mean C RMSD of 0.98[A] and 1.50[A] for the MHC chain and the peptide, respectively. The binding specificity is also predicted with high accuracy (mean AUC of 0.94). Furthermore, the structure modeling component is orders of magnitudes faster than state-of-the-art methods (modeling of 100,000 pMHCI pairs in four hours on a standard computer), enabling high-throughput applications for large immunopeptidomics datasets. While peptide-MHC specificity can be accurately predicted from the sequence alone, TCR specificity prediction likely requires modeling of the 3D structures. We anticipate our model can be further used in structure-based prediction of TCR specificity. MHCfold is available @https://github.com/dina-lab3D/MHCfold