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Diffusion analysis of single particle trajectories in a Bayesian nonparametrics framework

机译:贝叶斯非参数框架单粒子轨迹的扩散分析

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Single particle tracking (SPT), where individual molecules are fluorescently labelled and followed over time, is an important tool that allows the spatiotemporal dynamics of subcellular biological systems to be studied at very fine temporal and spatial resolution. Mathematical models of particle motion are typically based on Brownian diffusion, reflecting the noisy environment that biomolecules inhabit. In order to study changes in particle behaviour within individual tracks, Hidden Markov models (HMM) featuring multiple diffusive states have been used as a descriptive tool for SPT data. However, such models are typically specified with an a priori defined number of particle states and it has not been clear how such assumptions have affected their outcomes. Here, we propose a method for simultaneously inferring the number of diffusive states alongside the dynamic parameters governing particle motion. Our method is an infinite HMM (iHMM) with the general framework of Bayesian nonparametric models. We directly extend previous applications of these concepts in molecular biophysics to the SPT framework and propose and test an additional constraint with the goal of accelerating convergence and reducing computational time. We test our iHMM using simulated data and apply it to a previously analyzed large SPT dataset for B cell receptor motion on the plasma membrane of B cells of the immune system.
机译:单个粒子跟踪(SPT),其中单个分子被荧光标记并随后随后,是允许在非常精细的时间和空间分辨率下研究亚细胞生物系统的时空动态的重要工具。粒子运动的数学模型通常基于布朗扩散,反映了生物分子居住的嘈杂环境。为了研究单个轨道内的粒子行为的变化,具有多个扩散状态的隐藏的马尔可夫模型(HMM)已被用作SPT数据的描述性工具。然而,这种模型通常用先验定义数量的粒子状态指定,并且尚不清楚这些假设如何影响其结果。在这里,我们提出了一种用于同时推断在控制运动的动态参数旁边的扩散状态的数量。我们的方法是一种无限的嗯(IHMM),具有贝叶斯非参数模型的一般框架。我们直接将这些概念的先前应用在分子生物物理学中扩展到SPT框架,并提出并测试了加速收敛性和减少计算时间的额外约束。我们使用模拟数据测试我们的IHMM并将其应用于先前分析的B细胞受体运动的大型SPT数据集​​,用于免疫系统的B细胞的质膜。

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