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Modeling approaches for qualitative and semi-quantitative analysis of cellular signaling networks

机译:蜂窝信号网络定性和半定量分析的建模方法

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A central goal of systems biology is the construction of predictive models of bio-molecular networks. Cellular networks of moderate size have been modeled successfully in a quantitative way based on differential equations. However, in large-scale networks, knowledge of mechanistic details and kinetic parameters is often too limited to allow for the set-up of predictive quantitative models. Here, we review methodologies for qualitative and semi-quantitative modeling of cellular signal transduction networks. In particular, we focus on three different but related formalisms facilitating modeling of signaling processes with different levels of detail: interaction graphs, logical/Boolean networks, and logic-based ordinary differential equations (ODEs). Albeit the simplest models possible, interaction graphs allow the identification of important network properties such as signaling paths, feedback loops, or global interdependencies. Logical or Boolean models can be derived from interaction graphs by constraining the logical combination of edges. Logical models can be used to study the basic input–output behavior of the system under investigation and to analyze its qualitative dynamic properties by discrete simulations. They also provide a suitable framework to identify proper intervention strategies enforcing or repressing certain behaviors. Finally, as a third formalism, Boolean networks can be transformed into logic-based ODEs enabling studies on essential quantitative and dynamic features of a signaling network, where time and states are continuous. We describe and illustrate key methods and applications of the different modeling formalisms and discuss their relationships. In particular, as one important aspect for model reuse, we will show how these three modeling approaches can be combined to a modeling pipeline (or model hierarchy) allowing one to start with the simplest representation of a signaling network (interaction graph), which can later be refined to logical and eventually to logic-based ODE models. Importantly, systems and network properties determined in the rougher representation are conserved during these transformations.
机译:系统生物学的中心目标是构建生物分子网络的预测模型。基于微分方程,已经成功地以定量方式对中等大小的蜂窝网络进行了建模。但是,在大型网络中,对机械细节和动力学参数的了解通常太有限,以至于无法建立预测性定量模型。在这里,我们回顾了细胞信号传导网络的定性和半定量建模方法。特别地,我们关注于三种不同但相关的形式主义,这些模型促进了具有不同详细程度的信令过程的建模:交互图,逻辑/布尔网络和基于逻辑的常微分方程(ODE)。尽管可以使用最简单的模型,但交互图仍可以识别重要的网络属性,例如信令路径,反馈环路或全局相互依存关系。逻辑或布尔模型可以通过约束边的逻辑组合从交互图中得出。逻辑模型可用于研究被调查系统的基本输入输出行为,并通过离散仿真分析其定性动态特性。它们还提供了一个合适的框架,以识别实施或压制某些行为的适当干预策略。最后,作为第三种形式主义,布尔网络可以转换为基于逻辑的ODE,从而可以研究时间和状态连续的信令网络的基本定量和动态特征。我们描述和说明了不同建模形式主义的关键方法和应用,并讨论了它们之间的关系。特别是,作为模型重用的一个重要方面,我们将展示如何将这三种建模方法组合到一个建模管道(或模型层次结构)中,从而允许以最简单的信令网络表示(交互图)开始。后来将其改进为逻辑模型,并最终改进为基于逻辑的ODE模型。重要的是,在这些转换过程中,以粗略表示形式确定的系统和网络属性将得到保留。

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