Author:
Wu Yejian,Cao Lujing,Wu Zhipeng,Wu Xinyi,Wang Xinqiao,Duan Hongliang
Abstract
AbstractHuman major histocompatibility complex (MHC) proteins are encoded by the human leukocyte antigen (HLA) gene complex. When exogenous peptide fragments form peptide-HLA (pHLA) complexes with HLA molecules on the outer surface of cells, they can be recognized by T cells and trigger an immune response. Therefore, determining whether an HLA molecule can bind to a given peptide can improve the efficiency of vaccine design and facilitate the development of immunotherapy. This paper regards peptide fragments as natural language, we combine textCNN and BiLSTM to build a deep neural network model to encode the sequence features of HLA and peptides. Results on independent and external test datasets demonstrate that our CcBHLA model outperforms the state-of-the-art known methods in detecting HLA class I binding peptides. And the method is not limited by the HLA class I allele and the length of the peptide fragment. Users can download the model for binding peptide screening or retrain the model with private data on github (https://github.com/hongliangduan/CcBHLA-pan-specific-peptide-HLA-class-I-binding-prediction-via-Convolutional-and-BiLSTM-features.git).
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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