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PROBING BIOLOGICAL CELL NETWORKS USING MATHEMATICAL MODELS

机译:使用数学模型探测生物细胞网络

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Mathematical methods that we have used to analyze and help to identify the Planar Cell Polarity (PCP) signaling mechanism in fly wings are described. Often, in modeling biological signaling circuits such as this, only incomplete abstracted hypotheses exist to explain observed complex patterning. Thus, the development of mathematical models usually proceeds in iterative fashion, in which the structure of the model is chosen to represent certain hypotheses about how the system operates, and then parameters for this model are selected. In protein regulatory networks, the number of states to model is typically large and depends on the number of proteins of interest, the parameter spaces are large, and the most appropriate models are nonlinear. Therefore it is becoming increasingly important to develop fast, efficient, scalable methods for modeling in systems biology. In this paper, we present an overview of the biological questions being asked about PCP, a review of our earlier results in building models for PCP, as well as an algorithm for performing automatic parameter identification on differential equation models of biological systems. In the conference talk, we will additionally present new biological results and we will show how this model can be used to test a developmental hypothesis about the relationship between cell geometry and polarity.
机译:描述了我们用于分析和帮助在飞行翼中识别平面细胞极性(PCP)信号传导机制的数学方法。通常,在诸如此类的模拟生物信号电路中,仅存在不完整的抽象假设来解释观察到的复杂图案。因此,数学模型的发展通常以迭代方式进行,其中选择模型的结构来表示关于系统如何操作的某些假设,然后选择用于该模型的参数。在蛋白质调节网络中,模型的状态的数量通常很大并且取决于感兴趣的蛋白质的数量,参数空间很大,最合适的模型是非线性的。因此,开发用于在系统生物学建模的快速,高效,可扩展的方法越来越重要。在本文中,我们概述了关于PCP的生物学问题,对我们之前的结果进行了审查,该审查在构建PCP的模型中,以及用于在生物系统的微分方程模型上执行自动参数识别的算法。在会议谈话中,我们将另外提出新的生物学结果,我们将展示该模型如何用于测试关于细胞几何和极性之间关系的发展假设。

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