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首页> 外文期刊>The Journal of Chemical Physics >Multivariate moment closure techniques for stochastic kinetic models
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Multivariate moment closure techniques for stochastic kinetic models

机译:随机动力学模型的多元矩闭合技术

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Stochastic effects dominate many chemical and biochemical processes. Their analysis, however, can be computationally prohibitively expensive and a range of approximation schemes have been proposed to lighten the computational burden. These, notably the increasingly popular linear noise approximation and the more general moment expansion methods, perform well for many dynamical regimes, especially linear systems. At higher levels of nonlinearity, it comes to an interplay between the nonlinearities and the stochastic dynamics, which is much harder to capture correctly by such approximations to the true stochastic processes. Moment-closure approaches promise to address this problem by capturing higher-order terms of the temporally evolving probability distribution. Here, we develop a set of multivariate moment-closures that allows us to describe the stochastic dynamics of nonlinear systems. Multivariate closure captures the way that correlations between different molecular species, induced by the reaction dynamics, interact with stochastic effects. We use multivariate Gaussian, gamma, and lognormal closure and illustrate their use in the context of two models that have proved challenging to the previous attempts at approximating stochastic dynamics: oscillations in p53 and Hes1. In addition, we consider a larger system, Erk-mediated mitogen-activated protein kinases signalling, where conventional stochastic simulation approaches incur unacceptably high computational costs. (C) 2015 AIP Publishing LLC.
机译:随机效应主导着许多化学和生化过程。然而,他们的分析可能在计算上过于昂贵,并且提出了一系列近似方案以减轻计算负担。这些,尤其是越来越流行的线性噪声逼近和更通用的矩扩展方法,在许多动态范围,尤其是线性系统中表现良好。在较高的非线性水平下,它涉及到非线性和随机动力学之间的相互作用,而要通过这种近似真实的随机过程来正确地捕获它就很难了。矩闭合法有望通过捕获时间演化概率分布的高阶项来解决此问题。在这里,我们开发了一组多元矩闭合,使我们能够描述非线性系统的随机动力学。多变量闭合描述了由反应动力学引起的不同分子种类之间的相关性与随机效应相互作用的方式。我们使用多元高斯,伽玛和对数正态闭合,并说明了它们在两个模型中的使用情况,这两个模型已证明对先前尝试近似随机动力学具有挑战性:p53和Hes1中的振荡。此外,我们考虑了一个较大的系统,即Erk介导的丝裂原活化蛋白激酶信号传导,其中传统的随机模拟方法会导致无法接受的高计算成本。 (C)2015 AIP Publishing LLC。

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