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首页> 外文期刊>Computational Biology and Bioinformatics, IEEE/ACM Transactions on >Identification of Protein Complexes from Tandem Affinity Purification/Mass Spectrometry Data via Biased Random Walk
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Identification of Protein Complexes from Tandem Affinity Purification/Mass Spectrometry Data via Biased Random Walk

机译:通过偏向随机游走从串联亲和纯化/质谱数据中鉴定蛋白质复合物

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摘要

Systematic identification of protein complexes from protein-protein interaction networks (PPIs) is an important application of data mining in life science. Over the past decades, various new clustering techniques have been developed based on modelling PPIs as binary relations. Non-binary information of co-complex relations (prey/bait) in PPIs data derived from tandem affinity purification/mass spectrometry (TAP-MS) experiments has been unfairly disregarded. In this paper, we propose a Biased Random Walk based algorithm for detecting protein complexes from TAP-MS data, resulting in the random walk with restarting baits (RWRB). RWRB is developed based on Random walk with restart. The main contribution of RWRB is the incorporation of co-complex relations in TAP-MS PPI networks into the clustering process, by implementing a new restarting strategy during the process of random walk. Through experimentation on un-weighted and weighted TAP-MS data sets, we validated biological significance of our results by mapping them to manually curated complexes. Results showed that, by incorporating non-binary, co-membership information, significant improvement has been achieved in terms of both statistical measurements and biological relevance. Better accuracy demonstrates that the proposed method outperformed several state-of-the-art clustering algorithms for the detection of protein complexes in TAP-MS data.
机译:从蛋白质-蛋白质相互作用网络(PPI)进行蛋白质复合物的系统鉴定是生命科学中数据挖掘的重要应用。在过去的几十年中,基于将PPI建模为二进制关系,已经开发了各种新的聚类技术。源自串联亲和纯化/质谱(TAP-MS)实验的PPI数据中共复杂关系(猎物/诱饵)的非二进制信息已被不公平地忽视。在本文中,我们提出了一种基于偏向随机游走的算法,用于从TAP-MS数据中检测蛋白质复合物,从而导致带有重新启动诱饵(RWRB)的随机游走。 RWRB是基于随机游走并重新启动而开发的。 RWRB的主要贡献在于,通过在随机游走过程中实施新的重启策略,将TAP-MS PPI网络中的复杂问题纳入了集群过程。通过对未加权和加权的TAP-MS数据集进行实验,我们通过将结果映射到手动处理的复合物中来验证结果的生物学意义。结果表明,通过合并非二进制共同成员身份信息,在统计度量和生物学相关性方面都取得了显着改善。更好的准确性表明,该方法优于用于检测TAP-MS数据中蛋白质复合物的几种最新聚类算法。

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