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.

Highlights

  • None of the approaches described above have been used to model the interaction between a large bath of particles modeled by a continuous dynamic and a stochastic dynamic induced by rare events where few particles bind to small targets to trigger a response

  • Synchronous and asynchronous synaptic release might depend on calcium dynamics and we provide here several predictions using the present hybrid stochastic model of chemical reactions, that we compare to Gillespie simulations

  • The proposed mechanism of asynchronous vesicular release that we found here clarifies the role of calcium ions during short-term synaptic plasticity[9]

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Summary

Introduction

None of the approaches described above have been used to model the interaction between a large bath of particles modeled by a continuous dynamic and a stochastic dynamic induced by rare events where few particles bind to small targets to trigger a response. The goal of this report is to introduce a novel hybrid model and to provide an application to synaptic physiology for computing the probability of vesicular release following calcium influx. Calcium ions induce vesicular release when few of them accumulate underneath a vesicle. This accumulation can follow the direct influx at a short time scale or can be due to ions originating from the pre-synaptic terminal with a longer time scale. In all cases, triggering a vesicle release is a rare molecular event described as the accumulation of few ions at a single protein location[8]. Synchronous and asynchronous synaptic release might depend on calcium dynamics and we provide here several predictions using the present hybrid stochastic model of chemical reactions, that we compare to Gillespie simulations. The proposed mechanism of asynchronous vesicular release that we found here clarifies the role of calcium ions during short-term synaptic plasticity[9]

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