Millard Pierre, Portais Jean-Charles, Mendes Pedro
MCISB, Manchester Institute of Biotechnology, University of Manchester, Manchester, UK.
School of Computer Science, University of Manchester, Manchester, UK.
BMC Syst Biol. 2015 Sep 26;9:64. doi: 10.1186/s12918-015-0213-8.
Isotope labeling experiments (ILEs) are increasingly used to investigate the functioning of metabolic systems. Some enzymes are subject to kinetic isotope effects (KIEs) which modulate reaction rates depending on the isotopic composition of their substrate(s). KIEs may therefore affect both the propagation of isotopes through metabolic networks and their operation, and ultimately jeopardize the biological value of ILEs. However, the actual impact of KIEs on metabolism has never been investigated at the system level.
First, we developed a framework which integrates KIEs into kinetic and isotopic models of metabolism, thereby accounting for their system-wide effects on metabolite concentrations, metabolic fluxes, and isotopic patterns. Then, we applied this framework to assess the impact of KIEs on the central carbon metabolism of Escherichia coli in the context of (13)C-ILEs, under different situations commonly encountered in laboratories. Results showed that the impact of KIEs strongly depends on the label input and on the variable considered but is significantly lower than expected intuitively from measurements on isolated enzymes. The global robustness of both the metabolic operation and isotopic patterns largely emerge from intrinsic properties of metabolic networks, such as the distribution of control across the network and bidirectional isotope exchange.
These results demonstrate the necessity of investigating the impact of KIEs at the level of the entire system, contradict previous hypotheses that KIEs would have a strong effect on isotopic distributions and on flux determination, and strengthen the biological value of (13)C-ILEs. The proposed modeling framework is generic and can be used to investigate the impact of all the isotopic tracers ((2)H, (13)C, (15)N, (18)O, etc.) on different isotopic datasets and metabolic systems. By allowing the integration of isotopic and metabolomics data collected under stationary and/or non-stationary conditions, it may also assist interpretations of ILEs and facilitate the development of more accurate kinetic models with improved explicative and predictive capabilities.
同位素标记实验(ILEs)越来越多地用于研究代谢系统的功能。一些酶会受到动力学同位素效应(KIEs)的影响,这些效应会根据其底物的同位素组成来调节反应速率。因此,KIEs可能会影响同位素在代谢网络中的传播及其运作,并最终危及ILEs的生物学价值。然而,KIEs对代谢的实际影响从未在系统层面进行过研究。
首先,我们开发了一个框架,将KIEs整合到代谢的动力学和同位素模型中,从而考虑其对代谢物浓度、代谢通量和同位素模式的全系统影响。然后,我们应用这个框架,在实验室常见的不同情况下,评估KIEs对大肠杆菌中心碳代谢在(13)C-ILEs背景下的影响。结果表明,KIEs的影响强烈依赖于标记输入和所考虑的变量,但明显低于从对分离酶的测量中直观预期的值。代谢运作和同位素模式的整体稳健性很大程度上源于代谢网络的内在特性,如网络中控制的分布和双向同位素交换。
这些结果证明了在整个系统层面研究KIEs影响的必要性,与之前认为KIEs会对同位素分布和通量测定有强烈影响的假设相矛盾,并强化了(13)C-ILEs的生物学价值。所提出的建模框架具有通用性,可用于研究所有同位素示踪剂((2)H、(13)C、(15)N、(18)O等)对不同同位素数据集和代谢系统的影响。通过允许整合在稳态和/或非稳态条件下收集到的同位素和代谢组学数据,它还可能有助于ILEs的解释,并促进具有更高解释和预测能力的更精确动力学模型的开发。