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Towards an Integrated Protein-Protein Interaction Network

机译:迈向整合的蛋白质-蛋白质相互作用网络

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Protein-protein interactions play a major role in most cellular processes. Thus, the challenge of identifying the full repertoire of interacting proteins in the cell is of great importance, and has been addressed both experimentally and computationally. Today, large scale experimental studies of interacting proteins, while partial and noisy, allow us to characterize properties of interacting proteins and develop predictive algorithms. Most existing algorithms, however, ignore possible dependencies between interacting pairs, and predict them independently of one another. In this study, we present a computational approach that overcomes this drawback by predicting protein-protein interactions simultaneously. In addition, our approach allows us to integrate various protein attributes and explicitly account for uncertainty of assay measurements. Using the language of relational Markov Random Fields, we build a unified probabilistic model that includes all of these elements. We show how we can learn our model properties efficiently and then use it to predict all unobserved interactions simultaneously. Our results show that by modeling dependencies between interactions, as well as by taking into account protein attributes and measurement noise, we achieve a more accurate description of the protein interaction network. Furthermore, our approach allows us to gain new insights into the properties of interacting proteins.
机译:蛋白质-蛋白质相互作用在大多数细胞过程中起主要作用。因此,鉴定细胞中相互作用蛋白的全部组成的挑战非常重要,并且已经在实验和计算上得到解决。如今,对相互作用蛋白的大规模实验研究虽然部分且嘈杂,但使我们能够表征相互作用蛋白的特性并开发预测算法。但是,大多数现有算法都忽略了交互对之间可能的依赖关系,并相互独立地进行预测。在这项研究中,我们提出了一种计算方法,可以通过同时预测蛋白质与蛋白质的相互作用来克服这一缺点。此外,我们的方法使我们能够整合各种蛋白质属性,并明确说明测定方法的不确定性。使用关系马尔可夫随机场的语言,我们建立了一个包含所有这些要素的统一概率模型。我们展示了如何有效地学习模型属性,然后使用它来同时预测所有未观察到的交互。我们的结果表明,通过对相互作用之间的依赖性进行建模,并考虑到蛋白质属性和测量噪声,我们可以更准确地描述蛋白质相互作用网络。此外,我们的方法使我们对相互作用蛋白的性质有了新的认识。

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