Modular Control of Biological Networks

David Murrugarra, Alan Veliz-Cuba, Elena Dimitrova, Claus Kadelka, Matthew Wheeler, Reinhard Laubenbacher
{"title":"Modular Control of Biological Networks","authors":"David Murrugarra, Alan Veliz-Cuba, Elena Dimitrova, Claus Kadelka, Matthew Wheeler, Reinhard Laubenbacher","doi":"arxiv-2401.12477","DOIUrl":null,"url":null,"abstract":"The concept of control is central to understanding and applications of\nbiological network models. Some of their key structural features relate to\ncontrol functions, through gene regulation, signaling, or metabolic mechanisms,\nand computational models need to encode these. Applications of models often\nfocus on model-based control, such as in biomedicine or metabolic engineering.\nThis paper presents an approach to model-based control that exploits two common\nfeatures of biological networks, namely their modular structure and canalizing\nfeatures of their regulatory mechanisms. The paper focuses on intracellular\nregulatory networks, represented by Boolean network models. A main result of\nthis paper is that control strategies can be identified by focusing on one\nmodule at a time. This paper also presents a criterion based on canalizing\nfeatures of the regulatory rules to identify modules that do not contribute to\nnetwork control and can be excluded. For even moderately sized networks,\nfinding global control inputs is computationally very challenging. The modular\napproach presented here leads to a highly efficient approach to solving this\nproblem. This approach is applied to a published Boolean network model of blood\ncancer large granular lymphocyte (T-LGL) leukemia to identify a minimal control\nset that achieves a desired control objective.","PeriodicalId":501325,"journal":{"name":"arXiv - QuanBio - Molecular Networks","volume":"43 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Molecular Networks","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2401.12477","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

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.
生物网络的模块化控制
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。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信