bioRxiv (Cold Spring Harbor Laboratory) · 2018 · 130 citations · 38 references
Life SciencesBioinformaticsImmunologyComputational BiologyImmunogeneticsMolecular ImmunologyAlloantigen RecognitionAntigen RecognitionHuman Leukocyte Antigen SystemMajor Histocompatibility ComplexT Cell ActivationT Cell BiologyComputational Epitope PredictionConvolutional Neural NetworksPeptide-major Histocompatibility Complex RecognitionPrediction ModelsSequence PredictionSequence-based PredictionT Cell Epitope RecognitionT Cell Receptor Recognition
Predicting epitopes recognized by cytotoxic T cells has been a long standing challenge within the field of immuno- and bioinformatics. While reliable predictions of peptide binding are available for most Major Histocompatibility Complex class I (MHCI) alleles, prediction models of T cell receptor (TCR) interactions with MHC class I-peptide complexes remain poor due to the limited amount of available training data. Recent next generation sequencing projects have however generated a considerable amount of data relating TCR sequences with their cognate HLA-peptide complex target. Here, we utilize such data to train a sequence-based predictor of the interaction between TCRs and peptides presented by the most common human MHCI allele, HLA-A*02:01. Our model is based on convolutional neural networks, which are especially designed to meet the challenges posed by the large length variations of TCRs. We show that such a sequence-based model allows for the identification of TCRs binding a given cognate peptide-MHC target out of a large pool of non-binding TCRs.
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The immune epitope database (IEDB) 3.0
Randi Vita, James A. Overton, Jason Greenbaum et al. · Nucleic Acids Research · 2014 · 1.1K citations · Full text