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Predicting peptides that bind to MHC molecules using supervised learning of hidden Markov models.

机译:使用隐马尔可夫模型的监督学习预测结合MHC分子的肽。

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The binding of a major histocompatibility complex (MHC) molecule to a peptide originating in an antigen is essential to recognizing antigens in immune systems, and it has proved to be important to use computers to predict the peptides that will bind to an MHC molecule. The purpose of this paper is twofold: First, we propose to apply supervised learning of hidden Markov models (HMMs) to this problem, which can surpass existing methods for the problem of predicting MHC-binding peptides. Second, we generate peptides that have high probabilities to bind to a certain MHC molecule, based on our proposed method using peptides binding to MHC molecules as a set of training data. From our experiments, in a type of cross-validation test, the discrimination accuracy of our supervised learning method is usually approximately 2-15% better than those of other methods, including backpropagation neural networks, which have been regarded as the most effective approach to this problem. Furthermore, using an HMM trained for HLA-A2, we present new peptide sequences that are provided with high binding probabilities by the HMM and that are thus expected to bind to HLA-A2 proteins. Peptide sequences not shown in this paper but with rather high binding probabilities can be obtained from the author.
机译:主要组织相容性复合物(MHC)分子与起源于抗原的肽的结合对于识别免疫系统中的抗原是必不可少的,并且已证明使用计算机预测将与MHC分子结合的肽非常重要。本文的目的是双重的:首先,我们建议将隐马尔可夫模型(HMM)的监督学习应用于该问题,它可以超越现有的预测MHC结合肽的方法。第二,基于我们提出的使用结合MHC分子的肽作为一组训练数据的方法,我们生成具有高概率结合某些MHC分子的肽。根据我们的实验,在一种交叉验证测试中,我们的监督学习方法的判别准确度通常比其他方法(包括反向传播神经网络)高2-15%,后者被认为是最有效的方法。这个问题。此外,使用受过HLA-A2训练的HMM,我们提出了新的肽序列,这些新的肽序列被HMM提供了很高的结合概率,因此有望与HLA-A2蛋白结合。可以从作者处获得本文未显示但具有较高结合概率的肽序列。

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