Sadhukhan Priyanka P, Raghunathan Anu
Chemical Engineering Division, National Chemical Laboratory, Dr. Homi Bhabha Road, Pune, 411008, India.
Methods Mol Biol. 2014;1184:523-62. doi: 10.1007/978-1-4939-1115-8_29.
Genome Scale Metabolic Modeling methods represent one way to compute whole cell function starting from the genome sequence of an organism and contribute towards understanding and predicting the genotype-phenotype relationship. About 80 models spanning all the kingdoms of life from archaea to eukaryotes have been built till date and used to interrogate cell phenotype under varying conditions. These models have been used to not only understand the flux distribution in evolutionary conserved pathways like glycolysis and the Krebs cycle but also in applications ranging from value added product formation in Escherichia coli to predicting inborn errors of Homo sapiens metabolism. This chapter describes a protocol that delineates the process of genome scale metabolic modeling for analysing host-pathogen behavior and interaction using flux balance analysis (FBA). The steps discussed in the process include (1) reconstruction of a metabolic network from the genome sequence, (2) its representation in a precise mathematical framework, (3) its translation to a model, and (4) the analysis using linear algebra and optimization. The methods for biological interpretations of computed cell phenotypes in the context of individual host and pathogen models and their integration are also discussed.
基因组尺度代谢建模方法是一种从生物体的基因组序列出发计算全细胞功能的方式,有助于理解和预测基因型与表型的关系。迄今为止,已经构建了约80个涵盖从古菌到真核生物所有生命王国的模型,并用于探究不同条件下的细胞表型。这些模型不仅被用于理解糖酵解和三羧酸循环等进化保守途径中的通量分布,还被应用于从大肠杆菌中增值产物的形成到预测人类代谢先天性缺陷等各种领域。本章描述了一种协议,该协议使用通量平衡分析(FBA)描绘了用于分析宿主-病原体行为和相互作用的基因组尺度代谢建模过程。该过程中讨论的步骤包括:(1)从基因组序列重建代谢网络;(2)在精确的数学框架中对其进行表示;(3)将其转化为模型;(4)使用线性代数和优化进行分析。还讨论了在个体宿主和病原体模型背景下对计算出的细胞表型进行生物学解释的方法及其整合。