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PPI_SVM: Prediction of protein-protein interactions using machine learning domain-domain affinities and frequency tables

机译:PPI_SVM:使用机器学习域-域亲和力和频率表预测蛋白质-蛋白质相互作用

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摘要

Protein-protein interactions (PPI) control most of the biological processes in a living cell. In order to fully understand protein functions, a knowledge of protein-protein interactions is necessary. Prediction of PPI is challenging, especially when the three-dimensional structure of interacting partners is not known. Recently, a novel prediction method was proposed by exploiting physical interactions of constituent domains. We propose here a novel knowledge-based prediction method, namely PPI_SVM, which predicts interactions between two protein sequences by exploiting their domain information. We trained a two-class support vector machine on the benchmarking set of pairs of interacting proteins extracted from the Database of Interacting Proteins (DIP). The method considers all possible combinations of constituent domains between two protein sequences, unlike most of the existing approaches. Moreover, it deals with both single-domain proteins and multi domain proteins; therefore it can be applied to the whole proteome in high-throughput studies. Our machine learning classifier, following a brainstorming approach, achieves accuracy of 86%, with specificity of 95%, and sensitivity of 75%, which are better results than most previous methods that sacrifice recall values in order to boost the overall precision. Our method has on average better sensitivity combined with good selectivity on the benchmarking dataset. The PPI_SVM source code, train/test datasets and supplementary files are available freely in the public domain at: . Electronic Supplementary MaterialThe online version of this article (doi: 10.2478/s11658-011-0008-x contains supplementary material, which is available to authorized users.
机译:蛋白质-蛋白质相互作用(PPI)控制着活细胞中的大多数生物过程。为了充分理解蛋白质功能,必须具备蛋白质相互作用的知识。 PPI的预测具有挑战性,尤其是在未知相互作用伙伴的三维结构的情况下。最近,通过利用组成域的物理相互作用提出了一种新颖的预测方法。我们在这里提出一种新颖的基于知识的预测方法,即PPI_SVM,该方法通过利用两个蛋白质序列的域信息来预测它们之间的相互作用。我们在从相互作用蛋白数据库(DIP)中提取的相互作用蛋白对的基准对上训练了两类支持向量机。与大多数现有方法不同,该方法考虑了两个蛋白质序列之间组成域的所有可能组合。而且,它同时处理单结构域蛋白和多结构域蛋白。因此,它可以应用于高通量研究中的整个蛋白质组。我们的机器学习分类器采用了集思广益的方法,可达到86%的准确性,95%的特异性和75%的灵敏度,这比大多数以前为提高总体精度而牺牲召回率的方法要好。我们的方法在基准数据集上平均具有更好的灵敏度和良好的选择性。 PPI_SVM源代码,训练/测试数据集和补充文件可在公共领域免费获得,网址为:。电子补充材料本文的在线版本(doi:10.2478 / s11658-011-0008-x)包含补充材料,授权用户可以使用。

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