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Deep convolutional neural networks for pan-specific peptide-MHC class I binding prediction

机译:深卷积神经网络用于泛特异性肽-MHC I类结合预测

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摘要

BackgroundComputational scanning of peptide candidates that bind to a specific major histocompatibility complex (MHC) can speed up the peptide-based vaccine development process and therefore various methods are being actively developed. Recently, machine-learning-based methods have generated successful results by training large amounts of experimental data. However, many machine learning-based methods are generally less sensitive in recognizing locally-clustered interactions, which can synergistically stabilize peptide binding. Deep convolutional neural network (DCNN) is a deep learning method inspired by visual recognition process of animal brain and it is known to be able to capture meaningful local patterns from 2D images. Once the peptide-MHC interactions can be encoded into image-like array(ILA) data, DCNN can be employed to build a predictive model for peptide-MHC binding prediction. In this study, we demonstrated that DCNN is able to not only reliably predict peptide-MHC binding, but also sensitively detect locally-clustered interactions.
机译:背景技术与特定的主要组织相容性复合物(MHC)结合的候选肽的计算扫描可以加快基于肽的疫苗开发过程,因此正在积极开发各种方法。最近,通过训练大量的实验数据,基于机器学习的方法已产生成功的结果。但是,许多基于机器学习的方法通常在识别局部聚类的相互作用时不太敏感,这可以协同稳定肽的结合。深度卷积神经网络(DCNN)是一种受动物大脑视觉识别过程启发的深度学习方法,已知能够从2D图像中捕获有意义的局部模式。一旦可以将肽-MHC相互作用编码为图像样阵列(ILA)数据,就可以将DCNN用于建立肽-MHC结合预测的预测模型。在这项研究中,我们证明了DCNN不仅能够可靠地预测肽与MHC的结合,而且还可以灵敏地检测局部聚集的相互作用。

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