Savinell J M, Palsson B O
Department of Chemical Engineering, University of Michigan, Ann Arbor 48109-2136.
J Theor Biol. 1992 Mar 21;155(2):215-42. doi: 10.1016/s0022-5193(05)80596-x.
A method of analysis was presented in part I of this series for determining the fluxes in a biochemical network that are the optimal choices for experimental measurement. This algorithm is applied to two important biological models: Escherichia coli and a hybridoma cell line (167.4G5.3). Our results show that potentially poor choices for in vivo measurement of metabolic fluxes exist for both model systems. For the subset of reactions in E. coli that was studied, the condition number of the augmented stoichiometric matrix reveals that a 60-fold amplification of experimental error during computations is possible. The biochemical network of the hybridoma cell is more complex than the E. coli system, and thus results in much larger possible error amplification--up to 100,000-fold. The physiological situations appear to have sensitivities that are less than 1/4 to 1/10 of those estimated by the condition number, and the maximum sensitivities are proportional to the condition number. These maximum sensitivities calculated using estimates of the fluxes and the worst possible error vector are upper bounds on the system's actual sensitivity. By examining the effect of measurement error on the sensitivity, the most probable sensitivity is calculated. These results indicate that an approximate two-fold increase in sensitivity of the E. coli system is likely when the worst set of fluxes are measured rather than the best set. The most likely sensitivity of the hybridoma system can range three orders of magnitude, depending on the set of fluxes that are measured. The propagation of experimental error during computations can be diminished for both systems by increasing the number of flux measurements over and above the minimum number of experimental measurements. The findings from these two model systems indicate that the calculation of the condition number can be a useful method for efficient experimental design, and that the usefulness of this method increases as the order of the system increases.
本系列第一部分介绍了一种分析方法,用于确定生化网络中通量,这些通量是实验测量的最佳选择。该算法应用于两个重要的生物学模型:大肠杆菌和杂交瘤细胞系(167.4G5.3)。我们的结果表明,对于这两个模型系统,体内代谢通量测量都可能存在欠佳的选择。对于所研究的大肠杆菌反应子集,增广化学计量矩阵的条件数表明,计算过程中实验误差可能放大60倍。杂交瘤细胞的生化网络比大肠杆菌系统更复杂,因此导致可能的误差放大倍数更大——高达100,000倍。生理情况的敏感性似乎不到条件数估计值的1/4至1/10,且最大敏感性与条件数成正比。使用通量估计值和最坏可能误差向量计算出的这些最大敏感性是系统实际敏感性的上限。通过检查测量误差对敏感性的影响,计算出最可能的敏感性。这些结果表明,当测量最差的通量集而非最佳通量集时,大肠杆菌系统的敏感性可能会近似增加两倍。杂交瘤系统最可能的敏感性可能相差三个数量级,这取决于所测量的通量集。对于这两个系统,通过增加通量测量次数使其超过最小实验测量次数,可以减少计算过程中实验误差的传播。这两个模型系统的研究结果表明,条件数的计算可以作为一种有效的实验设计方法,并且随着系统阶数的增加,该方法的实用性也会增加。