SOFI-based 3D superresolution sectioning with a widefield microscope.

Thomas Dertinger, Jianmin Xu, Omeed Foroutan Naini, Robert Vogel, Shimon Weiss
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引用次数: 47

Abstract

Background: Fluorescence-based biological imaging has been revolutionized by the recent introduction of superresolution microscopy methods. 3D superresolution microscopy, however, remains a challenge as its implementation by existing superresolution methods is non-trivial.

Methods: Here we demonstrate a facile and straightforward 3D superresolution imaging and sectioning of the cytoskeletal network of a fixed cell using superresolution optical fluctuation imaging (SOFI) performed on a conventional lamp-based widefield microscope.

Results and conclusion: SOFI's inherent sectioning capability effectively transforms a conventional widefield microscope into a superresolution 'confocal widefield' microscope.

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基于sofi的宽视场显微镜三维超分辨切片。
背景:基于荧光的生物成像已经彻底改变了最近引入的超分辨率显微镜方法。然而,三维超分辨率显微镜仍然是一个挑战,因为现有的超分辨率方法实现它是不平凡的。方法:在这里,我们展示了一个简单和直接的3D超分辨率成像和切片的细胞骨架网络的固定细胞使用超分辨率光学波动成像(SOFI)进行传统的灯基宽视场显微镜。结果与结论:SOFI固有的切片能力有效地将传统的宽视场显微镜转变为超分辨率的“共焦宽视场”显微镜。
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Active Microscope Stabilization in Three Dimensions Using Image Correlation. Resolving the spatial relationship between intracellular components by dual color super resolution optical fluctuations imaging (SOFI). Blind assessment of localisation microscope image resolution GraspJ: an open source, real-time analysis package for super-resolution imaging SOFI-based 3D superresolution sectioning with a widefield microscope.
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