Riley D, Koutsoukos X, Riley K
Vanderbilt University, ISIS/EECS, Nashville, USA.
IET Syst Biol. 2009 May;3(3):137-54. doi: 10.1049/iet-syb.2008.0101.
Modelling and analysis of biochemical systems such as sugar cataract development (SCD) are critical because they can provide new insights into systems, which cannot be easily tested with experiments; however, they are challenging problems due to the highly coupled chemical reactions that are involved. The authors present a stochastic hybrid system (SHS) framework for modelling biochemical systems and demonstrate the approach for the SCD process. A novel feature of the framework is that it allows modelling the effect of drug treatment on the system dynamics. The authors validate the three sugar cataract models by comparing trajectories computed by two simulation algorithms. Further, the authors present a probabilistic verification method for computing the probability of sugar cataract formation for different chemical concentrations using safety and reachability analysis methods for SHSs. The verification method employs dynamic programming based on a discretisation of the state space and therefore suffers from the curse of dimensionality. To analyse the SCD process, a parallel dynamic programming implementation that can handle large, realistic systems was developed. Although scalability is a limiting factor, this work demonstrates that the proposed method is feasible for realistic biochemical systems.
对诸如糖性白内障发展(SCD)等生化系统进行建模和分析至关重要,因为它们能为那些难以通过实验轻易测试的系统提供新的见解;然而,由于所涉及的化学反应高度耦合,这些都是具有挑战性的问题。作者提出了一种用于生化系统建模的随机混合系统(SHS)框架,并展示了针对SCD过程的方法。该框架的一个新颖之处在于它允许对药物治疗对系统动力学的影响进行建模。作者通过比较两种模拟算法计算出的轨迹,对三种糖性白内障模型进行了验证。此外,作者提出了一种概率验证方法,使用SHS的安全性和可达性分析方法来计算不同化学浓度下糖性白内障形成的概率。该验证方法基于状态空间离散化采用动态规划,因此受到维度诅咒的困扰。为了分析SCD过程,开发了一种能够处理大型实际系统的并行动态规划实现。尽管可扩展性是一个限制因素,但这项工作表明所提出的方法对于实际生化系统是可行的。