Ideally, these additional constraints render the system
fully resolvable. Two main approaches exist for the interpretation of the determined 13C data and the calculation of intracellular flux distributions: Global isotopomer balancing [6,12,13,14] and metabolic flux ratio Selleck Cisplatin analysis [10,15]. Both approaches have their advantages and disadvantages as follows: In the global isotopomer ((mass) isotope isomer) balancing approach, metabolic fluxes are estimated from the isotopomer measurements by iteratively generating candidate flux distributions until they fit well to the experimental 13C labeling [6,12,13,14]. Inhibitors,research,lifescience,medical The challenge of this nonlinear optimization problem is to find the global optimum, which make this approach Inhibitors,research,lifescience,medical demanding in computation (time) and requires data of equally high accuracy as often all data are used unweighted. Existing software applying this approach include 13C-FLUX(2) [7,8] and OpenFLUX [6]. 13C-FLUX is a comprehensive tool enabling the analysis of different models Inhibitors,research,lifescience,medical and isotopic tracers. Besides the calculation of the flux distribution it offers a statistical analysis of the determined fluxes. Drawbacks of the software are its restriction to Linux or Unix OS, the requirement
of the user to specify free fluxes and initial guesses of the flux distribution, the manual initiation and termination of simulation runs and the demanding computation power and time. The Inhibitors,research,lifescience,medical updated version 13C-FLUX2 features several improvements such as reduced computation times, improved data exchange and flux distribution visualization. OpenFLUX, a completely open source MATLAB-based software, features facilitated model generation and short computation times applying the Elementary Metabolite Unit
algorithm. Inhibitors,research,lifescience,medical [15], also implemented in 13C-FLUX2. For both software packages 13C data have to be preprocessed externally. Metabolic flux ratio analysis, coined by Sauer as METAFoR [15], relies on the local interpretation of labeling data using probabilistic equations that constrain the ratios of fluxes producing the same metabolite. The approach is mainly independent of the global flux distribution in the entire metabolic network [15,17,18], MRIP with the consequence that flux ratios can be calculated without knowing the uptake and production rates of external metabolites and the biomass composition of the cell. If enough independent flux ratios can be identified, it is possible to use them to constrain the metabolic network equation system and to calculate the full flux distribution of the network [19]. In contrast to the global isotopomer approach, no exchange fluxes in reversible reactions can be calculated: one major disadvantage of this approach.