Wintermute Edwin H, Lieberman Tami D, Silver Pamela A
Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
BMC Syst Biol. 2013 Oct 3;7:98. doi: 10.1186/1752-0509-7-98.
Flux Balance Analysis is a theoretically elegant, computationally efficient, genome-scale approach to predicting biochemical reaction fluxes. Yet FBA models exhibit persistent mathematical degeneracy that generally limits their predictive power.
We propose a novel objective function for cellular metabolism that accounts for and exploits degeneracy in the metabolic network to improve flux predictions. In our model, regulation drives metabolism toward a region of flux space that allows nearly optimal growth. Metabolic mutants deviate minimally from this region, a function represented mathematically as a convex cone. Near-optimal flux configurations within this region are considered equally plausible and not subject to further optimizing regulation. Consistent with relaxed regulation near optimality, we find that the size of the near-optimal region predicts flux variability under experimental perturbation.
Accounting for suboptimal solutions can improve the predictive power of metabolic FBA models. Because fluctuations of enzyme and metabolite levels are inevitable, tolerance for suboptimality may support a functionally robust metabolic network.
通量平衡分析是一种理论上优雅、计算高效的全基因组规模方法,用于预测生化反应通量。然而,通量平衡分析模型表现出持续的数学退化,这通常限制了它们的预测能力。
我们提出了一种用于细胞代谢的新型目标函数,该函数考虑并利用代谢网络中的退化来改进通量预测。在我们的模型中,调控将代谢导向通量空间的一个区域,该区域允许近乎最优的生长。代谢突变体与该区域的偏差最小,该函数在数学上表示为一个凸锥。该区域内的近乎最优通量配置被认为同样合理,并且不受进一步的优化调控。与最优性附近的宽松调控一致,我们发现近乎最优区域的大小可预测实验扰动下的通量变异性。
考虑次优解可以提高代谢通量平衡分析模型的预测能力。由于酶和代谢物水平的波动是不可避免的,对次优性的耐受性可能支持功能稳健的代谢网络。