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通过受大脑启发的网络自动机理论对复杂网络中的自组织进行建模,可提高蛋白质互作组中的链接可靠性。

Modelling Self-Organization in Complex Networks Via a Brain-Inspired Network Automata Theory Improves Link Reliability in Protein Interactomes.

机构信息

Biomedical Cybernetics Group, Biotechnology Center (BIOTEC), Center for Molecular and Cellular Bioengineering (CMCB), Center for Systems Biology Dresden (CSBD), Department of Physics, Technische Universität Dresden, Tatzberg 47/49, 01307, Dresden, Germany.

Brain bio-inspired computing (BBC) lab, IRCCS Centro Neurolesi "Bonino Pulejo", Messina, Italy.

出版信息

Sci Rep. 2018 Oct 25;8(1):15760. doi: 10.1038/s41598-018-33576-8.

Abstract

Protein interactomes are epitomes of incomplete and noisy networks. Methods for assessing link-reliability using exclusively topology are valuable in network biology, and their investigation facilitates the general understanding of topological mechanisms and models to draw and correct complex network connectivity. Here, I revise and extend the local-community-paradigm (LCP). Initially detected in brain-network topological self-organization and afterward generalized to any complex network, the LCP is a theory to model local-topology-dependent link-growth in complex networks using network automata. Four novel LCP-models are compared versus baseline local-topology-models. It emerges that the reliability of an interaction between two proteins is higher: (i) if their common neighbours are isolated in a complex (local-community) that has low tendency to interact with other external proteins; (ii) if they have a low propensity to link with other proteins external to the local-community. These two rules are mathematically combined in C1*: a proposed mechanistic model that, in fact, outperforms the others. This theoretical study elucidates basic topological rules behind self-organization principia of protein interactomes and offers the conceptual basis to extend this theory to any class of complex networks. The link-reliability improvement, based on the mere topology, can impact many applied domains such as systems biology and network medicine.

摘要

蛋白质相互作用组是不完整和嘈杂网络的缩影。仅使用拓扑结构评估链路可靠性的方法在网络生物学中具有重要价值,对其研究有助于全面了解拓扑机制和模型,以绘制和纠正复杂网络的连通性。在这里,我修改并扩展了局部社区范式(LCP)。LCP 最初在大脑网络拓扑自组织中被检测到,后来被推广到任何复杂网络,它是一种使用网络自动机来模拟复杂网络中局部拓扑依赖链路增长的理论。将四个新的 LCP 模型与基线局部拓扑模型进行了比较。结果表明,如果两个蛋白质之间的相互作用具有以下特征,则其可靠性更高:(i)如果它们的共同邻居在一个具有低与其他外部蛋白质相互作用倾向的复杂(局部社区)中被隔离;(ii)如果它们与局部社区外的其他蛋白质连接的倾向较低。这两个规则在 C1*中被数学组合在一起:一个被提议的机制模型,实际上,它的性能优于其他模型。这项理论研究阐明了蛋白质相互作用组自组织原理背后的基本拓扑规则,并为将该理论扩展到任何复杂网络类别提供了概念基础。基于拓扑结构的链路可靠性改进,可以影响系统生物学和网络医学等许多应用领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68aa/6202355/d06ae56b95ad/41598_2018_33576_Fig1_HTML.jpg

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