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• W3044163929 abstract "Prediction of stable peptide binding to Class I HLAs is an important component for designing immunotherapies. While the best performing predictors are based on machine learning algorithms trained on peptide-HLA (pHLA) sequences, the use of structure for training predictors deserves further exploration. Given enough pHLA structures, a predictor based on the residue-residue interactions found in these structures has the potential to generalize for alleles with little or no experimental data. We have previously developed APE-Gen, a modeling approach able to produce pHLA structures in a scalable manner. In this work we use APE-Gen to model over 150,000 pHLA structures, the largest dataset of its kind, which were used to train a structure-based pan-allele model. We extract simple, homogenous features based on residue-residue distances between peptide and HLA, and build a random forest model for predicting stable pHLA binding. Our model achieves competitive AUROC values on leave-one-allele-out validation tests using significantly less data when compared to popular sequence-based methods. Additionally, our model offers an interpretation analysis that can reveal how the model composes the features to arrive at any given prediction. This interpretation analysis can be used to check if the model is in line with chemical intuition, and we showcase particular examples. Our work is a significant step towards using structure to achieve generalizable and more interpretable prediction for stable pHLA binding." @default.
• W3044163929 created "2020-07-29" @default.
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• W3044163929 date "2020-07-22" @default.
• W3044163929 modified "2023-10-17" @default.
• W3044163929 title "Large-Scale Structure-Based Prediction of Stable Peptide Binding to Class I HLAs Using Random Forests" @default.
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• W3044163929 doi "https://doi.org/10.3389/fimmu.2020.01583" @default.
• W3044163929 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7387700" @default.
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