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用于由罕见结合事件引起的细胞激活的混合马尔可夫-质量作用定律模型:应用于神经元突触处钙诱导的囊泡释放

Hybrid Markov-mass action law model for cell activation by rare binding events: Application to calcium induced vesicular release at neuronal synapses.

作者信息

Guerrier Claire, Holcman David

机构信息

Computational Biology and Applied Mathematics, Ecole Normale Supérieure Paris, France.

DAMTP and Churchill College, University of Cambridge, Cambridge CB30DS United Kingdom.

出版信息

Sci Rep. 2016 Oct 18;6:35506. doi: 10.1038/srep35506.

Abstract

Binding of molecules, ions or proteins to small target sites is a generic step of cell activation. This process relies on rare stochastic events where a particle located in a large bulk has to find small and often hidden targets. We present here a hybrid discrete-continuum model that takes into account a stochastic regime governed by rare events and a continuous regime in the bulk. The rare discrete binding events are modeled by a Markov chain for the encounter of small targets by few Brownian particles, for which the arrival time is Poissonian. The large ensemble of particles is described by mass action laws. We use this novel model to predict the time distribution of vesicular release at neuronal synapses. Vesicular release is triggered by the binding of few calcium ions that can originate either from the synaptic bulk or from the entry through calcium channels. We report here that the distribution of release time is bimodal although it is triggered by a single fast action potential. While the first peak follows a stimulation, the second corresponds to the random arrival over much longer time of ions located in the synaptic terminal to small binding vesicular targets. To conclude, the present multiscale stochastic modeling approach allows studying cellular events based on integrating discrete molecular events over several time scales.

摘要

分子、离子或蛋白质与小靶点的结合是细胞激活的一个普遍步骤。这一过程依赖于罕见的随机事件,即位于大量物质中的一个粒子必须找到小的且通常是隐藏的靶点。我们在此提出一种混合离散 - 连续体模型,该模型考虑了由罕见事件主导的随机状态以及大量物质中的连续状态。罕见的离散结合事件通过马尔可夫链进行建模,用于描述少数布朗粒子与小靶点的相遇,其到达时间呈泊松分布。大量粒子的集合则由质量作用定律描述。我们使用这个新模型来预测神经元突触处囊泡释放的时间分布。囊泡释放由少数钙离子的结合触发,这些钙离子可以来自突触大量物质,也可以通过钙通道进入。我们在此报告,尽管释放是由单个快速动作电位触发的,但释放时间的分布是双峰的。第一个峰值跟随刺激出现,第二个峰值则对应于位于突触末端的离子在更长时间内随机到达小的结合囊泡靶点。总之,当前的多尺度随机建模方法允许基于在多个时间尺度上整合离散分子事件来研究细胞事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c18/5067597/804db11b1970/srep35506-f1.jpg

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