...
首页> 外文期刊>Progress in Biophysics and Molecular Biology: An International Review Journal >Rule-based modeling and simulations of the inner kinetochore structure
【24h】

Rule-based modeling and simulations of the inner kinetochore structure

机译:基于规则的内部动粒结构建模和仿真

获取原文
获取原文并翻译 | 示例
           

摘要

Background: Combinatorial complexity is a central problem when modeling biochemical reaction networks, since the association of a few components can give rise to a large variation of protein complexes. Available classical modeling approaches are often insufficient for the analysis of very large and complex networks in detail. Recently, we developed a new rule-based modeling approach that facilitates the analysis of spatial and combinatorially complex problems. Here, we explore for the first time how this approach can be applied to a specific biological system, the human kinetochore, which is a multi-protein complex involving over 100 proteins. Results: Applying our freely available SRSim software to a large data set on kinetochore proteins in human cells, we construct a spatial rule-based simulation model of the human inner kinetochore. The model generates an estimation of the probability distribution of the inner kinetochore 3D architecture and we show how to analyze this distribution using information theory. In our model, the formation of a bridge between CenpA and an H3 containing nucleosome only occurs efficiently for higher protein concentration realized during S-phase but may be not in G1. Above a certain nucleosome distance the protein bridge barely formed pointing towards the importance of chromatin structure for kinetochore complex formation. We define a metric for the distance between structures that allow us to identify structural clusters. Using this modeling technique, we explore different hypothetical chromatin layouts. Conclusions: Applying a rule-based network analysis to the spatial kinetochore complex geometry allowed us to integrate experimental data on kinetochore proteins, suggesting a 3D model of the human inner kinetochore architecture that is governed by a combinatorial algebraic reaction network. This reaction network can serve as bridge between multiple scales of modeling. Our approach can be applied to other systems beyond kinetochores
机译:背景:在对生化反应网络进行建模时,组合复杂性是一个中心问题,因为少数组分的结合会引起蛋白质复合物的巨大变化。现有的经典建模方法通常不足以详细分析非常大和复杂的网络。最近,我们开发了一种新的基于规则的建模方法,该方法有助于对空间和组合复杂问题进行分析。在这里,我们首次探索了该方法如何应用于特定的生物系统,即人的线粒体,它是一种包含100多种蛋白质的多蛋白质复合物。结果:将我们免费提供的SRSim软件应用于人类细胞中线粒体蛋白的大量数据集,我们构建了基于空间规则的人体内线粒体模拟模型。该模型生成内部动线3D架构的概率分布的估计,并且我们展示了如何使用信息论来分析这种分布。在我们的模型中,CenpA和含有H3的核小体之间仅在S期实现较高的蛋白质浓度时才有效地形成桥,而在G1中可能没有。在一定的核小体距离以上,几乎没有形成蛋白质桥,这表明染色质结构对于动粒复合物形成的重要性。我们为结构之间的距离定义了一个度量标准,以使我们能够识别结构簇。使用这种建模技术,我们探索了不同的假设染色质布局。结论:将基于规则的网络分析应用于空间线粒体的复杂几何结构,使我们能够整合线粒体蛋白质的实验数据,从而提出了由组合代数反应网络控制的人类内部线粒体结构的3D模型。该反应网络可以充当多个建模规模之间的桥梁。我们的方法可以应用于动植物之外的其他系统

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号