Broeken Jordi, Johnson Hannah, Lidke Diane S, Liu Sheng, Nieuwenhuizen Robert P J, Stallinga Sjoerd, Lidke Keith A, Rieger Bernd
Quantitative Imaging Group, Department of Imaging Physics, Delft University of Technology, Lorentzweg 1, 2628 RE Delft, The Netherlands.
Department of Pathology, University of New Mexico, Albuquerque, NM 87106, USA.
Methods Appl Fluoresc. 2015 Mar;3(1):014003. doi: 10.1088/2050-6120/3/1/014003.
Inspired by recent developments in localization microscopy that applied averaging of identical particles in 2D for increasing the resolution even further, we discuss considerations for alignment (registration) methods for particles in general and for 3D in particular. We detail that traditional techniques for particle registration from cryo electron microscopy based on cross-correlation are not suitable, as the underlying image formation process is fundamentally different. We argue that only localizations, i.e. a set of coordinates with associated uncertainties, are recorded and not a continuous intensity distribution. We present a method that owes to this fact and that is inspired by the field of statistical pattern recognition. In particular we suggest to use an adapted version of the Bhattacharyya distance as a merit function for registration. We evaluate the method in simulations and demonstrate it on three-dimensional super-resolution data of Alexa 647 labelled to the Nup133 protein in the nuclear pore complex of Hela cells. From the simulations we find suggestions that for successful registration the localization uncertainty must be smaller than the distance between labeling sites on a particle. These suggestions are supported by theoretical considerations concerning the attainable resolution in localization microscopy and its scaling behavior as a function of labeling density and localization precision.
受近期定位显微镜技术发展的启发,该技术通过对二维中相同粒子进行平均以进一步提高分辨率,我们讨论了一般粒子尤其是三维粒子的对齐(配准)方法的相关考量。我们详细说明,基于互相关的传统冷冻电子显微镜粒子配准技术并不适用,因为其潜在的图像形成过程存在根本差异。我们认为记录的只是定位,即一组带有相关不确定性的坐标,而非连续的强度分布。基于这一事实,我们提出了一种受统计模式识别领域启发的方法。特别是,我们建议使用Bhattacharyya距离的适配版本作为配准的优值函数。我们在模拟中评估了该方法,并在HeLa细胞核孔复合体中用Alexa 647标记的Nup133蛋白的三维超分辨率数据上进行了演示。从模拟中我们发现,对于成功配准而言,定位不确定性必须小于粒子上标记位点之间的距离。这些建议得到了关于定位显微镜可达到的分辨率及其作为标记密度和定位精度函数的缩放行为的理论考量的支持。