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An HMM-based algorithm for evaluating rates of receptor–ligand binding kinetics from thermal fluctuation data

机译:基于HMM的算法可根据热波动数据评估受体-配体结合动力学的速率

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摘要

>Motivation: Abrupt reduction/resumption of thermal fluctuations of a force probe has been used to identify association/dissociation events of protein–ligand bonds. We show that off-rate of molecular dissociation can be estimated by the analysis of the bond lifetime, while the on-rate of molecular association can be estimated by the analysis of the waiting time between two neighboring bond events. However, the analysis relies heavily on subjective judgments and is time-consuming. To automate the process of mapping out bond events from thermal fluctuation data, we develop a hidden Markov model (HMM)-based method.>Results: The HMM method represents the bond state by a hidden variable with two values: bound and unbound. The bond association/dissociation is visualized and pinpointed. We apply the method to analyze a key receptor–ligand interaction in the early stage of hemostasis and thrombosis: the von Willebrand factor (VWF) binding to platelet glycoprotein Ibα (GPIbα). The numbers of bond lifetime and waiting time events estimated by the HMM are much more than those estimated by a descriptive statistical method from the same set of raw data. The kinetic parameters estimated by the HMM are in excellent agreement with those by a descriptive statistical analysis, but have much smaller errors for both wild-type and two mutant VWF-A1 domains. Thus, the computerized analysis allows us to speed up the analysis and improve the quality of estimates of receptor–ligand binding kinetics.>Contact: or
机译:>动机:力探针的热波动突然减少/恢复已经用于识别蛋白质-配体键的缔合/解离事件。我们表明,可以通过对键寿命的分析来估计分子解离的速率,而可以通过对两个相邻键事件之间的等待时间的分析来估计分子缔合的速率。但是,分析在很大程度上依赖于主观判断并且很费时间。为了自动化从热波动数据中映射键事件的过程,我们开发了一种基于隐马尔可夫模型(HMM)的方法。>结果: HMM方法通过具有两个值的隐藏变量表示键状态。 :绑定和未绑定。可视化并查明了键的关联/解离。我们应用该方法来分析止血和血栓形成早期的关键受体-配体相互作用:von Willebrand因子(VWF)与血小板糖蛋白Ibα(GPIbα)结合。 HMM估计的债券寿命和等待时间事件的数量远远多于通过描述性统计方法从同一组原始数据估计的数量。由HMM估算的动力学参数与描述性统计分析的动力学参数非常吻合,但对于野生型和两个突变VWF-A1域而言,误差都小得多。因此,计算机化的分析使我们能够加快分析速度并提高受体-配体结合动力学估计的质量。>联系方式

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