TITAN: T-cell receptor specificity prediction with bimodal attention networks

TITAN: предсказание специфичности T-клеточных рецепторов с помощью бимодальных сетей внимания
Anna Weber, Jannis Born, María Rodríguez Martínez
2021-04-26

Levenshtein-based k-nearest neighborsSMILES sequencesT-cell receptor specificity predictionTCR sequences and epitopesbimodal attention networks
MOTIVATION: The activity of the adaptive immune system is governed by T-cells and their specific T-cell receptors (TCR), which selectively recognize foreign antigens. Recent advances in experimental techniques have enabled sequencing of TCRs and their antigenic targets (epitopes), allowing to research the missing link between TCR sequence and epitope binding specificity. Scarcity of data and a large sequence space make this task challenging, and to date only models limited to a small set of epitopes have achieved good performance. Here, we establish a k-nearest-neighbor (K-NN) classifier as a strong baseline and then propose Tcr epITope bimodal Attention Networks (TITAN), a bimodal neural network that explicitly encodes both TCR sequences and epitopes to enable the independent study of generalization capabilities to unseen TCRs and/or epitopes. RESULTS: By encoding epitopes at the atomic level with SMILES sequences, we leverage transfer learning and data augmentation to enrich the input data space and boost performance. TITAN achieves high performance in the prediction of specificity of unseen TCRs (ROC-AUC 0.87 in 10-fold CV) and surpasses the results of the current state-of-the-art (ImRex) by a large margin. Notably, our Levenshtein-based K-NN classifier also exhibits competitive performance on unseen TCRs. While the generalization to unseen epitopes remains challenging, we report two major breakthroughs. First, by dissecting the attention heatmaps, we demonstrate that the sparsity of available epitope data favors an implicit treatment of epitopes as classes. This may be a general problem that limits unseen epitope performance for sufficiently complex models. Second, we show that TITAN nevertheless exhibits significantly improved performance on unseen epitopes and is capable of focusing attention on chemically meaningful molecular structures. AVAILABILITY AND IMPLEMENTATION: The code as well as the dataset used in this study is publicly available at https://github.com/PaccMann/TITAN. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
1
A Levenshtein-based k-nearest-neighbor classifier provides a strong baseline and remains competitive for predicting specificity of unseen TCRs.
2
Encoding epitopes as atomic-level SMILES sequences enables transfer learning and data augmentation, enriching the input space and improving specificity prediction.
3
Generalization to unseen epitopes remains difficult because sparse epitope data can cause complex models to implicitly treat epitopes as classes; nevertheless, TITAN improves performance and attends to chemically meaningful structures.
4
TITAN achieves ROC-AUC 0.87 in 10-fold cross-validation for unseen TCR specificity prediction and substantially outperforms the state-of-the-art ImRex model.
5
TITAN is a bimodal attention network that explicitly encodes both T-cell receptor sequences and epitopes to assess generalization to unseen receptors and epitopes.

T-cell receptors (TCRs) and their antigenic target epitopes

TCR–epitope binding specificity, including prediction and generalization to unseen TCRs and epitopes

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Publication Date
2021-04-26
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Authors
Anna Weber
Jannis Born
María Rodríguez Martínez
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