Department of Chemical and Biomolecular Engineering, Rice University, Houston, TX 77005, USA.
Metab Eng. 2010 Sep;12(5):429-45. doi: 10.1016/j.ymben.2010.05.003. Epub 2010 May 27.
The current state of the art for linear optimization in Flux Balance Analysis has been limited to single objective functions. Since mammalian systems perform various functions, a multiobjective approach is needed when seeking optimal flux distributions in these systems. In most of the available multiobjective optimization methods, there is a lack of understanding of when to use a particular objective, and how to combine and/or prioritize mutually competing objectives to achieve a truly optimal solution. To address these limitations we developed a soft constraints based linear physical programming-based flux balance analysis (LPPFBA) framework to obtain a multiobjective optimal solutions. The developed framework was first applied to compute a set of multiobjective optimal solutions for various pairs of objectives relevant to hepatocyte function (urea secretion, albumin, NADPH, and glutathione syntheses) in bioartificial liver systems. Next, simultaneous analysis of the optimal solutions for three objectives was carried out. Further, this framework was utilized to obtain true optimal conditions to improve the hepatic functions in a simulated bioartificial liver system. The combined quantitative and visualization framework of LPPFBA is applicable to any large-scale metabolic network system, including those derived by genomic analyses.
通量平衡分析中线性优化的最新技术一直局限于单目标函数。由于哺乳动物系统执行各种功能,因此在寻求这些系统中的最佳通量分布时需要采用多目标方法。在大多数可用的多目标优化方法中,缺乏对何时使用特定目标以及如何组合和/或优先考虑相互竞争的目标以实现真正的最优解的理解。为了解决这些限制,我们开发了一种基于软约束的线性物理规划通量平衡分析(LPPFBA)框架来获得多目标最优解。首先,将开发的框架应用于计算生物人工肝系统中与肝细胞功能(尿素分泌、白蛋白、NADPH 和谷胱甘肽合成)相关的各种目标对的一组多目标最优解。接下来,对三个目标的最优解进行了同时分析。此外,该框架还用于获得真实的最优条件,以改善模拟生物人工肝系统中的肝功能。LPPFBA 的综合定量和可视化框架适用于任何大规模代谢网络系统,包括通过基因组分析得出的系统。