挖掘蛋白质相互作用组网络测量相互作用可靠性和选择枢纽蛋白

Young-Rae Cho, A. Zhang
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引用次数: 10

摘要

高通量技术涉及蛋白质-蛋白质相互作用的大规模检测。从基因组尺度的角度来看,这些相互作用数据集被构建成一个相互作用组网络。由于相互作用证据代表功能联系,各种图论计算方法已被应用于相互作用组网络的功能表征。然而,这些数据通常是不可靠的,并且典型的全基因组相互作用组网络具有复杂的连通性。本文对蛋白质相互作用组网络进行了系统分析,提出了一种$k$圆信号流仿真算法,从相互作用组网络的连接模式来衡量相互作用的可靠性。该算法通过模拟信息信号在复杂连接中的传播,定量表征蛋白质之间的功能联系。在这方面,该算法有效地估计了每个交互的备选路径的强度。作者还提出了一种挖掘复杂交互体网络结构的算法。该算法通过节点的分层排序对网络进行重构,这种结构重构过程揭示了相互作用体网络中的枢纽蛋白。本文论证了两轮仿真从本体相关性和功能一致性两个方面对交互可靠性进行了准确评分。最后,作者验证了所选择的结构枢纽代表功能核心蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mining Protein Interactome Networks to Measure Interaction Reliability and Select Hub Proteins
High-throughput techniques involve large-scale detection of protein-protein interactions. This interaction data set from the genome-scale perspective is structured into an interactome network. Since the interaction evidence represents functional linkage, various graph-theoretic computational approaches have been applied to the interactome networks for functional characterization. However, this data is generally unreliable, and the typical genome-wide interactome networks have a complex connectivity. In this paper, the authors explore systematic analysis of protein interactome networks, and propose a $k$-round signal flow simulation algorithm to measure interaction reliability from connection patterns of the interactome networks. This algorithm quantitatively characterizes functional links between proteins by simulating the propagation of information signals through complex connections. In this regard, the algorithm efficiently estimates the strength of alternative paths for each interaction. The authors also present an algorithm for mining the complex interactome network structure. The algorithm restructures the network by hierarchical ordering of nodes, and this structure re-formatting process reveals hub proteins in the interactome networks. This paper demonstrates that two rounds of simulation accurately scores interaction reliability in terms of ontological correlation and functional consistency. Finally, the authors validate that the selected structural hubs represent functional core proteins.
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