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囊泡运输和细胞骨架的空间建模:走对路的挑战。

Spatial modeling of vesicle transport and the cytoskeleton: the challenge of hitting the right road.

机构信息

Automatic Control Laboratory, Swiss Federal Institute of Technology Zurich, Zurich, Switzerland.

出版信息

PLoS One. 2012;7(1):e29645. doi: 10.1371/journal.pone.0029645. Epub 2012 Jan 12.

DOI:10.1371/journal.pone.0029645
PMID:22253752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3257240/
Abstract

The membrane trafficking machinery provides a transport and sorting system for many cellular proteins. We propose a mechanistic agent-based computer simulation to integrate and test the hypothesis of vesicle transport embedded into a detailed model cell. The method tracks both the number and location of the vesicles. Thus both the stochastic properties due to the low numbers and the spatial aspects are preserved. The underlying molecular interactions that control the vesicle actions are included in a multi-scale manner based on the model of Heinrich and Rapoport (2005). By adding motor proteins we can improve the recycling process of SNAREs and model cell polarization. Our model also predicts that coat molecules should have a high turnover at the compartment membranes, while the turnover of motor proteins has to be slow. The modular structure of the underlying model keeps it tractable despite the overall complexity of the vesicle system. We apply our model to receptor-mediated endocytosis and show how a polarized cytoskeleton structure leads to polarized distributions in the plasma membrane both of SNAREs and the Ste2p receptor in yeast. In addition, we can couple signal transduction and membrane trafficking steps in one simulation, which enables analyzing the effect of receptor-mediated endocytosis on signaling.

摘要

膜运输机制为许多细胞蛋白提供了运输和分拣系统。我们提出了一种基于机制的基于代理的计算机模拟,以整合和测试嵌入详细模型细胞中的囊泡运输假说。该方法不仅可以跟踪囊泡的数量,还可以跟踪其位置。因此,既保留了由于数量低而导致的随机性,又保留了空间方面。基于 Heinrich 和 Rapoport(2005)的模型,以多尺度的方式包含了控制囊泡作用的基本分子相互作用。通过添加马达蛋白,我们可以改善 SNARE 的回收过程并模拟细胞极化。我们的模型还预测,外壳分子在隔室膜上应该具有高周转率,而马达蛋白的周转率必须很慢。尽管囊泡系统的整体复杂性很高,但基础模型的模块化结构使其易于处理。我们将模型应用于受体介导的内吞作用,并展示了极化细胞骨架结构如何导致质膜中 SNARE 和酵母中 Ste2p 受体的极化分布。此外,我们可以在一次模拟中耦合信号转导和膜运输步骤,从而能够分析受体介导的内吞作用对信号转导的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fbf/3257240/08395724600e/pone.0029645.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fbf/3257240/f30cbe01bf3c/pone.0029645.g001.jpg
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