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A comparative study of high resolution microscopy imaging modalities using a three-dimensional resolution measure

机译:使用三维分辨率测量的高分辨率显微镜成像模态的比较研究

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摘要

From an acquired image, single molecule microscopy makes possible the determination of the distance separating two closely spaced biomolecules in three-dimensional (3D) space. Such distance information can be an important indicator of the nature of the biomolecular interaction. Distance determination, however, is especially difficult when, for example, the imaged point sources are very close to each other or are located near the focal plane of the imaging setup. In the context of such challenges, we compare the limits of the distance estimation accuracy for several high resolution 3D imaging modalities. The comparisons are made using a Cramer-Rao lower bound-based 3D resolution measure which predicts the best possible accuracy with which a given distance can be estimated. Modalities which separate the detection of individual point sources (e.g., using photoactivatable fluorophores) are shown to provide the best accuracy limits when the two point sources are very close to each other and/or are oriented near parallel to the optical axis. Meanwhile, modalities which implement the simultaneous imaging of the point sources from multiple focal planes perform best when given a near-focus point source pair. We also demonstrate that the maximum likelihood estimator is capable of attaining the limit of the accuracy predicted for each modality.
机译:从获取的图像中,单分子显微镜可以确定在三维(3D)空间中分隔两个紧密间隔的生物分子的距离。这样的距离信息可以是生物分子相互作用的性质的重要指标。然而,例如当成像的点源彼此非常接近或位于成像装置的焦平面附近时,距离确定尤其困难。在此类挑战的背景下,我们比较了几种高分辨率3D成像模态的距离估计精度的局限性。使用基于Cramer-Rao下界的3D分辨率度量进行比较,该度量可预测可估计给定距离的最佳精度。当两个点源彼此非常靠近和/或平行于光轴取向时,示出了分离检测单个点源的方式(例如,使用可光激活的荧光团)提供了最佳的精度极限。同时,在给定近焦点点源对时,实现从多个焦平面对点源进行同时成像的模态效果最佳。我们还证明了最大似然估计器能够达到每种模态预测的准确性极限。

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