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Iteration method for predicting essential proteins based on orthology and protein-protein interaction networks

机译:基于正交学和蛋白质-蛋白质相互作用网络的基本蛋白质迭代预测方法

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Background Identification of essential proteins plays a significant role in understanding minimal requirements for the cellular survival and development. Many computational methods have been proposed for predicting essential proteins by using the topological features of protein-protein interaction (PPI) networks. However, most of these methods ignored intrinsic biological meaning of proteins. Moreover, PPI data contains many false positives and false negatives. To overcome these limitations, recently many research groups have started to focus on identification of essential proteins by integrating PPI networks with other biological information. However, none of their methods has widely been acknowledged. Results By considering the facts that essential proteins are more evolutionarily conserved than nonessential proteins and essential proteins frequently bind each other, we propose an iteration method for predicting essential proteins by integrating the orthology with PPI networks, named by ION. Differently from other methods, ION identifies essential proteins depending on not only the connections between proteins but also their orthologous properties and features of their neighbors. ION is implemented to predict essential proteins in S. cerevisiae. Experimental results show that ION can achieve higher identification accuracy than eight other existing centrality methods in terms of area under the curve (AUC). Moreover, ION identifies a large amount of essential proteins which have been ignored by eight other existing centrality methods because of their low-connectivity. Many proteins ranked in top 100 by ION are both essential and belong to the complexes with certain biological functions. Furthermore, no matter how many reference organisms were selected, ION outperforms all eight other existing centrality methods. While using as many as possible reference organisms can improve the performance of ION. Additionally, ION also shows good prediction performance in E. coli K-12. Conclusions The accuracy of predicting essential proteins can be improved by integrating the orthology with PPI networks.
机译:背景必需蛋白质的鉴定在理解细胞存活和发育的最低要求方面起着重要作用。已经提出了许多利用蛋白质-蛋白质相互作用(PPI)网络的拓扑特征预测必需蛋白质的计算方法。但是,这些方法大多数都忽略了蛋白质的内在生物学意义。此外,PPI数据包含许多假阳性和假阴性。为了克服这些局限性,最近许多研究小组已开始通过将PPI网络与其他生物学信息相结合来专注于鉴定必需蛋白。但是,没有一种方法被广泛认可。结果通过考虑基本蛋白比非必需蛋白和基本蛋白经常结合的事实,我们提出了一种迭代方法,通过将正畸学与PPI网络集成在一起来预测基本蛋白,该方法被称为ION。与其他方法不同,ION不仅根据蛋白质之间的联系,还取决于其直系同源特性和邻居特征来鉴定必需蛋白质。实施ION可以预测酿酒酵母中的必需蛋白质。实验结果表明,就曲线下面积(AUC)而言,ION可以比其他八种现有的中心方法获得更高的识别精度。此外,ION识别出大量必需蛋白质,这些蛋白质由于其低连接性而被其他八种现有的中心化方法所忽略。 ION排在前100位的许多蛋白质都是必不可少的,属于具有某些生物学功能的复合物。此外,无论选择了多少参考生物,ION的性能都优于其他所有八个现有的中心化方法。在使用尽可能多的参考生物的同时,可以提高ION的性能。此外,ION在大肠杆菌K-12中也显示出良好的预测性能。结论通过将正畸学与PPI网络集成,可以提高预测必需蛋白质的准确性。

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