The Delft Bioinformatics Lab, Department of Intelligent Systems, Delft University of Technology, Delft, The Netherlands.
PLoS One. 2012;7(7):e39396. doi: 10.1371/journal.pone.0039396. Epub 2012 Jul 9.
Understanding cellular regulation of metabolism is a major challenge in systems biology. Thus far, the main assumption was that enzyme levels are key regulators in metabolic networks. However, regulation analysis recently showed that metabolism is rarely controlled via enzyme levels only, but through non-obvious combinations of hierarchical (gene and enzyme levels) and metabolic regulation (mass action and allosteric interaction). Quantitative analyses relating changes in metabolic fluxes to changes in transcript or protein levels have revealed a remarkable lack of understanding of the regulation of these networks. We study metabolic regulation via feasibility analysis (FA). Inspired by the constraint-based approach of Flux Balance Analysis, FA incorporates a model describing kinetic interactions between molecules. We enlarge the portfolio of objectives for the cell by defining three main physiologically relevant objectives for the cell: function, robustness and temporal responsiveness. We postulate that the cell assumes one or a combination of these objectives and search for enzyme levels necessary to achieve this. We call the subspace of feasible enzyme levels the feasible enzyme space. Once this space is constructed, we can study how different objectives may (if possible) be combined, or evaluate the conditions at which the cells are faced with a trade-off among those. We apply FA to the experimental scenario of long-term carbon limited chemostat cultivation of yeast cells, studying how metabolism evolves optimally. Cells employ a mixed strategy composed of increasing enzyme levels for glucose uptake and hexokinase and decreasing levels of the remaining enzymes. This trade-off renders the cells specialized in this low-carbon flux state to compete for the available glucose and get rid of over-overcapacity. Overall, we show that FA is a powerful tool for systems biologists to study regulation of metabolism, interpret experimental data and evaluate hypotheses.
理解细胞代谢调控是系统生物学的一个主要挑战。到目前为止,主要假设是酶水平是代谢网络的关键调节剂。然而,最近的调控分析表明,代谢很少通过酶水平来控制,而是通过层次(基因和酶水平)和代谢调控(质量作用和变构相互作用)的非明显组合来控制。将代谢通量的变化与转录物或蛋白质水平的变化相关联的定量分析揭示了对这些网络调控的理解的显著缺乏。我们通过可行性分析(FA)来研究代谢调控。受通量平衡分析的约束方法的启发,FA 结合了一个描述分子间动力学相互作用的模型。我们通过定义细胞的三个主要生理相关目标(功能、鲁棒性和时间响应性)来扩大细胞的目标组合。我们假设细胞采用一个或多个这些目标,并寻找实现这些目标所需的酶水平。我们将可行的酶水平的子空间称为可行的酶空间。一旦构建了这个空间,我们就可以研究不同的目标如何(如果可能的话)组合,或者评估细胞在这些目标之间面临权衡的条件。我们将 FA 应用于酵母细胞长期碳限制恒化器培养的实验场景,研究代谢如何最优地进化。细胞采用了一种混合策略,包括增加葡萄糖摄取和己糖激酶的酶水平,以及降低其余酶的水平。这种权衡使细胞专门适应这种低碳通量状态,以竞争可用的葡萄糖并摆脱过度产能。总的来说,我们表明 FA 是系统生物学家研究代谢调控、解释实验数据和评估假设的有力工具。