论文标题

通过扩散影响的可逆结合的第一阶段方法:对纳米级信号的见解

A first-passage approach to diffusion-influenced reversible binding: insights into nanoscale signaling at the presynapse

论文作者

Reva, Maria, DiGregorio, David A., Grebenkov, Denis S.

论文摘要

神经元之间的突触传播受一系列随机反应扩散事件的控制,这些事件导致钙诱导的囊泡释放神经递质。由于由于其纳米表和亚毫秒量表的实验测量,该系统的实验性测量很具有挑战性,但尽管计算限制了限制,但数值模拟仍然是研究依赖钙依赖性突触小囊泡融合的主要工具。在本文中,我们开发了一种分析解决方案,以基于第一分时间的时间迅速探索动态随机反应扩散问题。这是第一个同时考虑钙离子扩散,缓冲及其与囊泡传感器的结合/解开反应的相关统计特征的分析模型。特别是,未结合动力学对钙传感器的占用概率具有重大影响,因此不能忽略。使用蒙特卡洛模拟,我们验证了我们的分析溶液,用于瞬时钙涌入,并通过电压门控钙通道进行了验证。总体而言,我们提出了一种快速而严格的分析工具来研究简化的反应扩散系统,该系统允许以分子尺度对生物物理参数进行系统的探索,同时正确地考虑了细胞内分子相互作用的统计性质,这也可以作为更通用的细胞信号模拟器的构建块。

Synaptic transmission between neurons is governed by a cascade of stochastic reaction-diffusion events that lead to calcium-induced vesicle release of neurotransmitter. Since experimental measurements of such systems are challenging due their nanometer and sub-millisecond scale, numerical simulations remain the principal tool for studying calcium dependent synaptic vesicle fusion, despite limitations of time-consuming calculations. In this paper we develop an analytical solution to rapidly explore dynamical stochastic reaction-diffusion problems, based on first-passage times. This is the first analytical model that accounts simultaneously for relevant statistical features of calcium ion diffusion, buffering, and its binding/unbinding reaction with a vesicular sensor. In particular, unbinding kinetics are shown to have a major impact on the calcium sensor's occupancy probability on a millisecond scale and therefore cannot be neglected. Using Monte Carlo simulations we validated our analytical solution for instantaneous calcium influx and that through voltage-gated calcium channels. Overall we present a fast and rigorous analytical tool to study simplified reaction-diffusion systems that allow a systematic exploration of the biophysical parameters at a molecular scale, while correctly accounting for the statistical nature of molecular interactions within cells, that can also serve as a building block for more general cell signaling simulators.

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