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Mining protein interactomes to improve their reliability and support the advancement of network medicine

机译:挖掘蛋白质相互作用组以提高其可靠性并支持网络医学的发展

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摘要

High-throughput detection of protein interactions has had a major impact in our understanding of the intricate molecular machinery underlying the living cell, and has permitted the construction of very large protein interactomes. The protein networks that are currently available are incomplete and a significant percentage of their interactions are false positives. Fortunately, the structural properties observed in good quality social or technological networks are also present in biological systems. This has encouraged the development of tools, to improve the reliability of protein networks and predict new interactions based merely on the topological characteristics of their components. Since diseases are rarely caused by the malfunction of a single protein, having a more complete and reliable interactome is crucial in order to identify groups of inter-related proteins involved in disease etiology. These system components can then be targeted with minimal collateral damage. In this article, an important number of network mining tools is reviewed, together with resources from which reliable protein interactomes can be constructed. In addition to the review, a few representative examples of how molecular and clinical data can be integrated to deepen our understanding of pathogenesis are discussed.
机译:蛋白质相互作用的高通量检测对我们对活细胞潜在的复杂分子机制的理解产生了重大影响,并允许构建非常大的蛋白质相互作用组。当前可用的蛋白质网络不完整,相互作用的很大一部分是假阳性。幸运的是,在高质量的社会或技术网络中观察到的结构特性也存在于生物系统中。这鼓励了工具的开发,以提高蛋白质网络的可靠性并仅根据其组成部分的拓扑特征预测新的相互作用。由于疾病很少是由单个蛋白质的功能失常引起的,因此,为了鉴定出与疾病病因有关的相互关联的蛋白质组,拥有更完整和可靠的相互作用组至关重要。然后,这些系统组件可以以最小的附带损害作为目标。在本文中,回顾了许多重要的网络挖掘工具,以及可用于构建可靠的蛋白质相互作用组的资源。除了该综述之外,还讨论了一些有关如何整合分子和临床数据以加深我们对发病机理的理解的代表性例子。

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