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Analytical derivation of moment equations in stochastic chemical kinetics

机译:随机化学动力学中矩方程的解析推导

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摘要

The master probability equation captures the dynamic behavior of a variety of stochastic phenomena that can be modeled as Markov processes. Analytical solutions to the master equation are hard to come by though because they require the enumeration of all possible states and the determination of the transition probabilities between any two states. These two tasks quickly become intractable for all but the simplest of systems. Instead of determining how the probability distribution changes in time, we can express the master probability distribution as a function of its moments, and, we can then write transient equations for the probability distribution moments. In 1949, Moyal defined the derivative, or jump, moments of the master probability distribution. These are measures of the rate of change in the probability distribution moment values, i.e. what the impact is of any given transition between states on the moment values. In this paper we present a general scheme for deriving analytical moment equations for any N-dimensional Markov process as a function of the jump moments. Importantly, we propose a scheme to derive analytical expressions for the jump moments for any N-dimensional Markov process. To better illustrate the concepts, we focus on stochastic chemical kinetics models for which we derive analytical relations for jump moments of arbitrary order. Chemical kinetics models are widely used to capture the dynamic behavior of biological systems. The elements in the jump moment expressions are a function of the stoichiometric matrix and the reaction propensities, i.e. the probabilistic reaction rates. We use two toy examples, a linear and a non-linear set of reactions, to demonstrate the applicability and limitations of the scheme. Finally, we provide an estimate on the minimum number of moments necessary to obtain statistical significant data that would uniquely determine the dynamics of the underlying stochastic chemical kinetic system. The first two moments only provide limited information, especially when complex, non-linear dynamics are involved.
机译:主概率方程式可捕获各种随机现象的动态行为,这些行为可以建模为马尔可夫过程。尽管很难求出主方程的解析解,因为它们需要枚举所有可能的状态以及确定任何两个状态之间的转换概率。除了最简单的系统,这两个任务很快变得棘手。无需确定概率分布随时间变化的方式,我们可以将主概率分布表示为其矩的函数,然后可以为概率分布矩写瞬态方程。 1949年,Moyal定义了主概率分布的导数或跳跃矩。这些是概率分布矩值的变化率的度量,即状态之间任何给定过渡对矩值的影响。在本文中,我们提出了一个通用方案,用于推导任何N维马尔可夫过程的解析矩方程,并将其作为跳跃矩的函数。重要的是,我们提出了一种方案,可以为任何N维Markov过程推导跳跃矩的解析表达式。为了更好地说明这些概念,我们关注于随机化学动力学模型,通过该模型我们可以得出任意阶跃矩的解析关系。化学动力学模型被广泛用于捕获生物系统的动力学行为。跳跃力矩表达式中的元素是化学计量矩阵和反应倾向即概率反应速率的函数。我们使用两个玩具示例(线性和非线性反应集)来证明该方案的适用性和局限性。最后,我们提供了获得必要的最小矩数的估计,这些统计数据将唯一确定潜在的随机化学动力学系统的动力学。前两个时刻仅提供有限的信息,尤其是在涉及复杂的非线性动力学时。

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