EPIC-TRACE: predicting TCR binding to unseen epitopes using attention and contextualized embeddings
EPIC-TRACE: прогнозирование связывания TCR с ранее не встречавшимися эпитопами с использованием механизмов внимания и контекстуализированных эмбеддингов
2023-12-01
SCID: 54.1/m5sm9t3u
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ProtBERT embeddingsTCR binding predictionmulti-head attentionpeptide-MHC complexesunseen epitopes
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Abstract (AI)
MOTIVATION: T cells play an essential role in adaptive immune system to fight pathogens and cancer but may also give rise to autoimmune diseases. The recognition of a peptide-MHC (pMHC) complex by a T cell receptor (TCR) is required to elicit an immune response. Many machine learning models have been developed to predict the binding, but generalizing predictions to pMHCs outside the training data remains challenging. RESULTS: We have developed a new machine learning model that utilizes information about the TCR from both α and β chains, epitope sequence, and MHC. Our method uses ProtBERT embeddings for the amino acid sequences of both chains and the epitope, as well as convolution and multi-head attention architectures. We show the importance of each input feature as well as the benefit of including epitopes with only a few TCRs to the training data. We evaluate our model on existing databases and show that it compares favorably against other state-of-the-art models. AVAILABILITY AND IMPLEMENTATION: https://github.com/DaniTheOrange/EPIC-TRACE.
Key Findings
1
EPIC-TRACE predicts TCR binding to unseen epitopes using information from both TCR α and β chains, epitope sequences, and MHC.
2
Feature analyses demonstrate the importance of the model’s input components for predicting TCR–pMHC binding.
3
Including epitopes associated with only a few TCRs improves training and supports better generalization beyond observed training data.
4
On existing databases, EPIC-TRACE compares favorably with other state-of-the-art TCR-binding prediction models.
5
The model combines ProtBERT contextualized amino-acid embeddings with convolutional and multi-head attention architectures.
Research Object
T-cell receptor (TCR) binding to peptide–MHC (pMHC) complexes, including unseen epitopes
Research Subject
Generalization and prediction of TCR–pMHC binding specificity to unseen epitopes using information from TCR α/β chains, epitope sequences, and MHC
Publication Details
Publication Date
2023-12-01
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