薄层荧光显微镜
显微镜
显微镜
荧光显微镜
各向同性
光学
生物成像
生物标本
材料科学
人工智能
计算机科学
扫描共焦电子显微镜
荧光
物理
作者
Fang Zhao,Lanxin Zhu,Chunyu Fang,Tingting Yu,Dan Zhu,Peng Fei
摘要
Isotropic 3D histological imaging of large biological specimens is highly desired but remains highly challenging to current fluorescence microscopy technique. Here we present a new method, termed deep-learning super-resolution light-sheet add-on microscopy (Deep-SLAM), to enable fast, isotropic light-sheet fluorescence imaging on a conventional wide-field microscope. After integrating a minimized add-on device that transforms an inverted microscope into a 3D light-sheet microscope, we further integrate a deep neural network (DNN) procedure to quickly restore the ambiguous z-reconstructed planes that suffer from still insufficient axial resolution of light-sheet illumination, thereby achieving isotropic 3D imaging of thick biological specimens at single-cell resolution. We apply this easy and cost-effective Deep-SLAM approach to the anatomical imaging of single neurons in a meso-scale mouse brain, demonstrating its potential for readily converting commonly-used commercialized 2D microscopes to high-throughput 3D imaging, which is previously exclusive for high-end microscopy implementations.
科研通智能强力驱动
Strongly Powered by AbleSci AI