DISMA-Dipartimento di Scienze Matematiche "G.L. Lagrange", Politecnico di Torino, Torino, Italy.
Department of Mathematics, California State University San Marcos, San Marcos, USA.
Math Biosci Eng. 2022 May 24;19(8):7649-7668. doi: 10.3934/mbe.2022359.
Reaction networks are widely used models to describe biochemical processes. Stochastic fluctuations in the counts of biological macromolecules have amplified consequences due to their small population sizes. This makes it necessary to favor stochastic, discrete population, continuous time models. The stationary distributions provide snapshots of the model behavior at the stationary regime, and as such finding their expression in terms of the model parameters is of great interest. The aim of the present paper is to describe when the stationary distributions of the original model, whose state space is potentially infinite, coincide exactly with the stationary distributions of the process truncated to finite subsets of states, up to a normalizing constant. The finite subsets of states we identify are called copies and are inspired by the modular topology of reaction network models. With such a choice we prove a novel graphical characterization of the concept of complex balancing for stochastic models of reaction networks. The results of the paper hold for the commonly used mass-action kinetics but are not restricted to it, and are in fact stated for more general setting.
反应网络被广泛用于描述生化过程。由于生物大分子的数量较少,其计数的随机波动会产生放大的后果。这使得必须优先考虑随机的、离散的种群、连续时间模型。固定分布提供了模型在固定状态下的行为快照,因此,以模型参数的形式找到它们的表达式是非常有意义的。本文的目的是描述当潜在无限状态空间的原始模型的固定分布与固定子集的状态截断过程的固定分布完全一致时,除了一个归一化常数。我们确定的状态的有限子集称为副本,并受到反应网络模型模块化拓扑的启发。通过这样的选择,我们证明了用于反应网络随机模型的复杂平衡概念的一种新的图形特征。本文的结果适用于常用的质量作用动力学,但不仅限于此,实际上是针对更一般的情况提出的。