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Dynamic Modelling of Mitochondrial Metabolism ?

机译:线粒体代谢的动态建模

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Mitochondria are cellular organelles that harbour complex biochemical processes ranging from ATP production to calcium signalling, and a purely experimental approach is insufficient to understand the intricate interactions of these processes.In this work, we develop a dynamic model of the mammalian mitochondrial metabolic processes in the form of coupled ordinary differential equations. The model includes the oxidative phosphorylation (OxPhos) complexes, the Krebs cycle, and the metabolites reactions and transport.First, we improved an existing OxPhos model (see Heiske et al. (2017)) by taking into account appropriate enzyme kinetics and thermodynamics, describing each complex by a separate rate equation. These equations are coupled in a mitochondria model context and parameterised using literature data from isolated mitochondria and parameter adjustment of a previous OxPhos data set in Heiske et al. (2017). Then, we coupled the OxPhos model with an adjusted model of metabolites transport and the Krebs cycle similar to Wu et al. (2007).Due to the non-identifiability of some parameters, we propose to use a collinearity-integer optimization workflow presented by Gábor et al. (2017) to find the characteristics of the non-identifiable parameters, thus reformulating and validating the model accordingly.
机译:线粒体是港口细胞器,其港口复杂的生物化学过程从ATP生产到钙信号传导,并且纯粹的实验方法不足以了解这些过程的错综复杂的相互作用。在这项工作中,我们开发了哺乳动物线粒体代谢过程的动态模型耦合常微分方程的形式。该模型包括氧化磷酸化(奥汤膦)复合物,克雷布斯循环和代谢物反应和运输。我们改进了现有的毒物模型(参见希斯克等人。(参见Heiske等人)通过考虑合适的酶动力学和热力学,通过单独的速率方程描述每个复合物。这些等式在线粒体模型上下文中耦合,并使用来自隔离线粒体的文献数据和参数调整在希伊克等人中设置的参数调整。 (2017)。然后,我们通过调整后的代谢物运输模型和类似于Wu等人的Krebs循环耦合奥帕洛斯模型。 (2007)。向某些参数的不可识别性,我们建议使用Gábor等人提供的Conslinity-Integer优化工作流程。 (2017)找到不可识别参数的特征,从而相应地重新重新格式化和验证模型。

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