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Multiple events on single molecules: Unbiased estimation in single-molecule biophysics

机译:单分子上的多个事件:单分子生物物理学中的无偏估计

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摘要

Most analyses of single-molecule experiments consist of binning experimental outcomes into a histogram and finding the parameters that optimize the fit of this histogram to a given data model. Here we show that such an approach can introduce biases in the estimation of the parameters, thus great care must be taken in the estimation of model parameters from the experimental data. The bias can be particularly large when the observations themselves are not statistically independent and are subjected to global constraints, as, for example, when the iterated steps of a motor protein acting on a single molecule must not exceed the total molecule length. We have developed a maximum-likelihood analysis, respecting the experimental constraints, which allows for a robust and unbiased estimation of the parameters, even when the bias well exceeds 100%. We demonstrate the potential of the method for a number of single-molecule experiments, focusing on the removal of DNA supercoils by topoisomerase IB, and validate the method by numerical simulation of the experiment.
机译:对单分子实验的大多数分析都包括将实验结果合并到直方图中,并找到优化该直方图与给定数据模型的拟合度的参数。在这里我们表明,这种方法会在参数估计中引入偏差,因此在从实验数据估计模型参数时必须格外小心。当观测值本身在统计上不是独立的并且受到全局约束时,例如,当作用于单个分子的运动蛋白的迭代步骤不得超过总分子长度时,偏差可能会特别大。我们已经开发了一种最大似然分析,同时考虑了实验约束,即使偏差超过100%,也可以对参数进行可靠且无偏的估计。我们展示了该方法在许多单分子实验中的潜力,重点在于通过拓扑异构酶IB去除DNA超螺旋,并通过实验的数值模拟验证了该方法。

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