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首页> 外文期刊>Frontiers in Molecular Biosciences >Delayed Comparison and Apriori Algorithm (DCAA): A Tool for Discovering Protein–Protein Interactions From Time-Series Phosphoproteomic Data
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Delayed Comparison and Apriori Algorithm (DCAA): A Tool for Discovering Protein–Protein Interactions From Time-Series Phosphoproteomic Data

机译:延迟比较和APRIORI算法(DCAA):一种从时间序列磷蛋白数据中发现蛋白质 - 蛋白质相互作用的工具

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Analysis of high-throughput omics data is one of the most important approaches for obtaining information regarding interactions between proteins/genes. Time-series omics data are a series of omics data points indexed in time order and normally contain more abundant information about the interactions between biological macromolecules than static omics data. Additionally, phosphorylation is a key posttranslational modification (PTM) that is indicative of possible protein function changes in cellular processes. Analysis of time-series phosphoproteomic data should provide more meaningful information about protein interactions. However, although many algorithms, databases and websites have been developed to analyze omics data, the tools dedicated to discovering molecular interactions from time-series omics data, especially from time-series phosphoproteomic data, are still scarce. Moreover, most reported tools ignore the lag between functional alterations and the corresponding changes in protein synthesis/PTM and are highly dependent on prior knowledge, resulting in high false-positive rates and difficulties in finding newly discovered protein-protein interactions (PPIs). Therefore, in the present study, we developed a new method to discover protein-protein interactions with the delayed comparison and Apriori algorithm (DCAA) to address the abovementioned problems. DCAA is based on the idea that there is a lag between functional alterations and the corresponding changes in protein synthesis/PTM. The Apriori algorithm was used to mine association rules from the relationships between items in a dataset and find PPIs based on time-series phosphoproteomic data. The advantage of DCAA is that it does not rely on prior knowledge and the PPI database. The analysis of actual time-series phosphoproteomic data showed that more than 68% of the protein interactions/regulatory relationships predicted by DCAA were accurate. As an analytical tool for PPIs that does not rely on a priori knowledge, DCAA should be useful to predict PPIs from time-series omics data, and this approach is not limited to phosphoproteomic data.
机译:高通量OMICS数据的分析是获得关于蛋白质/基因之间的相互作用的最重要的方法之一。时间序列OMICS数据是一系列以时间顺序索引的OMIC数据点,并且通常包含关于生物大分子之间的交互的更多信息,而不是静态常规数据。另外,磷酸化是一种关键的后期改变(PTM),其指示可能的细胞过程中可能的蛋白质功能变化。时间序列磷蛋白质数据的分析应提供有关蛋白质相互作用的更有意义的信息。然而,尽管已经开发了许多算法,数据库和网站来分析OMICS数据,但是专用于发现从时间序列OMIC数据的分子交互的工具,尤其是从时序磷蛋白质数据,仍然稀缺。此外,大多数报道的工具忽略了功能改变和蛋白质合成/ PTM的相应变化之间的滞后,并且高度依赖于先前知识,导致在寻找新发现的蛋白质 - 蛋白质相互作用(PPI)方面具有高的假阳性率和困难。因此,在本研究中,我们开发了一种发现与延迟比较和APRiori算法(DCAA)发现蛋白质 - 蛋白质相互作用以解决上述问题的新方法。 DCAA基于功能改变与蛋白质合成/ PTM的相应变化之间存在滞后。 APRiori算法用于从数据集中项目之间的关系之间的关系挖掘关联规则,并基于时间级磷蛋白蛋白酶数据找到PPI。 DCAA的优势在于它不依赖于先验知识和PPI数据库。对实际时间级磷蛋白酶数据的分析表明,DCAA预测的超过68%的蛋白质相互作用/调节关系是准确的。作为不依赖于先验知识的PPI的分析工具,DCAA应该有助于预测从时间序列OMIC数据的PPI,并且该方法不限于磷蛋白蛋白质数据。

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