生物网络的模块化控制

David Murrugarra, Alan Veliz-Cuba, Elena Dimitrova, Claus Kadelka, Matthew Wheeler, Reinhard Laubenbacher
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引用次数: 0

摘要

控制的概念是理解和应用生物网络模型的核心。它们的一些关键结构特征与控制功能有关,如基因调控、信号传导或代谢机制,而计算模型需要对这些功能进行编码。模型的应用通常侧重于基于模型的控制,如在生物医学或代谢工程中的应用。本文介绍了一种基于模型的控制方法,它利用了生物网络的两个共同特征,即模块化结构和调控机制的渠化特征。本文的重点是以布尔网络模型为代表的细胞内调控网络。本文的一个主要结果是,可以通过一次只关注一个模块来确定控制策略。本文还提出了一种基于调控规则渠化特征的标准,用于识别无助于网络控制并可被排除的模块。即使对于中等规模的网络,寻找全局控制输入在计算上也非常具有挑战性。本文介绍的模块化方法是解决这一问题的高效方法。本文将这种方法应用于已发表的血癌大颗粒淋巴细胞(T-LGL)白血病布尔网络模型,以确定能实现预期控制目标的最小控制集。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modular Control of Biological Networks
The concept of control is central to understanding and applications of biological network models. Some of their key structural features relate to control functions, through gene regulation, signaling, or metabolic mechanisms, and computational models need to encode these. Applications of models often focus on model-based control, such as in biomedicine or metabolic engineering. This paper presents an approach to model-based control that exploits two common features of biological networks, namely their modular structure and canalizing features of their regulatory mechanisms. The paper focuses on intracellular regulatory networks, represented by Boolean network models. A main result of this paper is that control strategies can be identified by focusing on one module at a time. This paper also presents a criterion based on canalizing features of the regulatory rules to identify modules that do not contribute to network control and can be excluded. For even moderately sized networks, finding global control inputs is computationally very challenging. The modular approach presented here leads to a highly efficient approach to solving this problem. This approach is applied to a published Boolean network model of blood cancer large granular lymphocyte (T-LGL) leukemia to identify a minimal control set that achieves a desired control objective.
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