具有可逆反应的非结构网格反应-漂移-扩散主方程。

IF 2 4区 数学 Q2 BIOLOGY Bulletin of Mathematical Biology Pub Date : 2024-12-09 DOI:10.1007/s11538-024-01392-z
Samuel A Isaacson, Ying Zhang
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引用次数: 0

摘要

我们建立了一个收敛的反应-漂移-扩散主方程(CRDDME),以方便研究在一般区域几何中由于一体势场而引起的空间输运受漂移影响的反应过程。通过两个步骤得到广义的CRDDME。我们首先推导了可逆扩散的非结构化网格跳跃过程近似,从而能够模拟漂移-扩散过程,其中漂移是由于偏颇粒子运动的保守场引起的。利用边缘平均有限元方法,我们的方法保留了平衡状态下漂移扩散通量的详细平衡,并保留了在非结构化网格上经历漂移扩散的粒子的平衡吉布斯-玻尔兹曼分布。接下来,我们为形式为a + B↔C的可逆反应建立了一个基于粒子的空间连续体积反应性反应-漂移-扩散模型。采用有限体积离散法对模型中的反应项进行了跳跃过程逼近。离散化是为了确保反应-漂移-扩散组合跳跃过程近似与保持在平衡状态的反应通量的详细平衡相一致,同时支持连续平衡状态的离散版本。新的CRDDME模型是对基础体积反应性模型的连续时间离散空间跳跃过程近似。我们通过一些数值例子证明了新的CRDDME的收敛性和准确性,并说明了它在T细胞信号传导中膜蛋白受体动力学的理想模型中的应用。
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An Unstructured Mesh Reaction-Drift-Diffusion Master Equation with Reversible Reactions.

We develop a convergent reaction-drift-diffusion master equation (CRDDME) to facilitate the study of reaction processes in which spatial transport is influenced by drift due to one-body potential fields within general domain geometries. The generalized CRDDME is obtained through two steps. We first derive an unstructured grid jump process approximation for reversible diffusions, enabling the simulation of drift-diffusion processes where the drift arises due to a conservative field that biases particle motion. Leveraging the Edge-Averaged Finite Element method, our approach preserves detailed balance of drift-diffusion fluxes at equilibrium, and preserves an equilibrium Gibbs-Boltzmann distribution for particles undergoing drift-diffusion on the unstructured mesh. We next formulate a spatially-continuous volume reactivity particle-based reaction-drift-diffusion model for reversible reactions of the form A + B C . A finite volume discretization is used to generate jump process approximations to reaction terms in this model. The discretization is developed to ensure the combined reaction-drift-diffusion jump process approximation is consistent with detailed balance of reaction fluxes holding at equilibrium, along with supporting a discrete version of the continuous equilibrium state. The new CRDDME model represents a continuous-time discrete-space jump process approximation to the underlying volume reactivity model. We demonstrate the convergence and accuracy of the new CRDDME through a number of numerical examples, and illustrate its use on an idealized model for membrane protein receptor dynamics in T cell signaling.

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来源期刊
CiteScore
3.90
自引率
8.60%
发文量
123
审稿时长
7.5 months
期刊介绍: The Bulletin of Mathematical Biology, the official journal of the Society for Mathematical Biology, disseminates original research findings and other information relevant to the interface of biology and the mathematical sciences. Contributions should have relevance to both fields. In order to accommodate the broad scope of new developments, the journal accepts a variety of contributions, including: Original research articles focused on new biological insights gained with the help of tools from the mathematical sciences or new mathematical tools and methods with demonstrated applicability to biological investigations Research in mathematical biology education Reviews Commentaries Perspectives, and contributions that discuss issues important to the profession All contributions are peer-reviewed.
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