Structural identifiability of biomolecular controller motifs with and without flow measurements as model output.

IF 4.3 2区 生物学
PLoS Computational Biology Pub Date : 2023-08-28 eCollection Date: 2023-08-01 DOI:10.1371/journal.pcbi.1011398
Eivind S Haus, Tormod Drengstig, Kristian Thorsen
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引用次数: 0

Abstract

Controller motifs are simple biomolecular reaction networks with negative feedback. They can explain how regulatory function is achieved and are often used as building blocks in mathematical models of biological systems. In this paper we perform an extensive investigation into structural identifiability of controller motifs, specifically the so-called basic and antithetic controller motifs. Structural identifiability analysis is a useful tool in the creation and evaluation of mathematical models: it can be used to ensure that model parameters can be determined uniquely and to examine which measurements are necessary for this purpose. This is especially useful for biological models where parameter estimation can be difficult due to limited availability of measureable outputs. Our aim with this work is to investigate how structural identifiability is affected by controller motif complexity and choice of measurements. To increase the number of potential outputs we propose two methods for including flow measurements and show how this affects structural identifiability in combination with, or in the absence of, concentration measurements. In our investigation, we analyze 128 different controller motif structures using a combination of flow and/or concentration measurements, giving a total of 3648 instances. Among all instances, 34% of the measurement combinations provided structural identifiability. Our main findings for the controller motifs include: i) a single measurement is insufficient for structural identifiability, ii) measurements related to different chemical species are necessary for structural identifiability. Applying these findings result in a reduced subset of 1568 instances, where 80% are structurally identifiable, and more complex/interconnected motifs appear easier to structurally identify. The model structures we have investigated are commonly used in models of biological systems, and our results demonstrate how different model structures and measurement combinations affect structural identifiability of controller motifs.

具有和不具有作为模型输出的流量测量的生物分子控制器基序的结构可识别性。
控制器基序是具有负反馈的简单生物分子反应网络。它们可以解释调节功能是如何实现的,并且经常被用作生物系统数学模型的构建块。在本文中,我们对控制器基元的结构可识别性进行了广泛的研究,特别是所谓的基本和对偶控制器基元。结构可识别性分析是创建和评估数学模型的有用工具:它可以用于确保模型参数可以唯一确定,并检查为此目的需要进行哪些测量。这对于由于可测量输出的可用性有限而难以进行参数估计的生物模型尤其有用。我们这项工作的目的是研究结构可识别性如何受到控制器基序复杂性和测量选择的影响。为了增加潜在输出的数量,我们提出了两种包括流量测量的方法,并展示了这如何影响与浓度测量相结合或在没有浓度测量的情况下的结构可识别性。在我们的研究中,我们使用流量和/或浓度测量的组合分析了128种不同的控制器基序结构,总共给出了3648个实例。在所有实例中,34%的测量组合提供了结构可识别性。我们对控制器基序的主要发现包括:i)单个测量不足以实现结构可识别性,ii)与不同化学物种相关的测量对于结构可识别是必要的。应用这些发现减少了1568个实例的子集,其中80%在结构上是可识别的,并且更复杂/互连的基序似乎更容易在结构上识别。我们研究的模型结构通常用于生物系统的模型,我们的结果证明了不同的模型结构和测量组合如何影响控制器基元的结构可识别性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PLoS Computational Biology
PLoS Computational Biology 生物-生化研究方法
CiteScore
7.10
自引率
4.70%
发文量
820
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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