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SPDM - Single Molecule Superresolution of Cellular Nanostructures

机译:SPDM-细胞纳米结构的单分子超分辨率

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Novel methods of visible light microscopy have overcome the limits of resolution hitherto thought to be insurmountable. The localization microscopy technique presented here based on the principles of Spectral Precision Distance Microscopy (SPDM) with conventional fluorophores under special physical conditions allows to measure the spatial distribution of single fluorescence labeled molecules in entire cells with macromolecular precision which is comparable to a macromolecular effective optical resolution. Based on detection of single molecules, in a novel combination of SPDM and Spatially Modulated Illumination (SMI) microscopy, a lateral (2D) effective optical resolution of cellular nanostructures around 10-20 nm (about 1/50th of the exciting wavelength) and a three dimensional (3D) effective optical resolution in the range of 40 - 50 nm are achieved.
机译:可见光显微镜的新方法已经克服了迄今为止认为不可克服的分辨率限制。此处介绍的基于光谱精确距离显微镜(SPDM)原理的定位显微镜技术与常规荧光团在特殊的物理条件下结合使用,能够以大分子精度测量整个细胞中单个荧光标记分子的空间分布,这与大分子有效光学技术相当解析度。基于对单个分子的检测,在SPDM和空间调制照明(SMI)显微镜的新颖结合中,细胞纳米结构的横向(2D)有效光学分辨率约为10-20 nm(激发波长的1/50左右),并且实现了40-50 nm范围内的三维(3D)有效光学分辨率。

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