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投影斜平面结构照明显微镜

Projective oblique plane structured illumination microscopy.

作者信息

Chang Bo-Jui, Shepherd Douglas, Fiolka Reto

机构信息

Lyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.

Center for Biological Physics and Department of Physics, Arizona State University, Tempe, AZ, 82587, USA.

出版信息

Npj Imaging. 2023 Nov 28;1(1):2. doi: 10.1038/s44303-023-00002-2.

Abstract

Structured illumination microscopy (SIM) can double the spatial resolution of a fluorescence microscope and video rate live cell imaging in a two-dimensional format has been demonstrated. However, rapid implementations of 2D SIM typically only cover a narrow slice of the sample immediately at the coverslip, with most of the cellular volume out of reach. Here, we implement oblique plane structured illumination microscopy (OPSIM) in a projection format to rapidly image an entire cell in a 2D SIM framework. As no mechanical scanning of the sample or objective is involved, this technique has the potential for rapid projection imaging with doubled resolution. We characterize the spatial resolution with fluorescent nanospheres, compare projection and 3D imaging using OPSIM and image mitochondria and ER dynamics across an entire cell at up to 2.7 Hz. To our knowledge, this represents the fastest whole cell SIM imaging to date.

摘要

结构照明显微镜(SIM)可以将荧光显微镜的空间分辨率提高一倍,并且已经证明了以二维格式进行视频速率的活细胞成像。然而,二维SIM的快速实现通常仅覆盖盖玻片处紧邻的样品窄切片,大部分细胞体积无法触及。在这里,我们以投影格式实现斜平面结构照明显微镜(OPSIM),以便在二维SIM框架中快速对整个细胞进行成像。由于不涉及样品或物镜的机械扫描,该技术具有以两倍分辨率进行快速投影成像的潜力。我们用荧光纳米球表征空间分辨率,使用OPSIM比较投影成像和三维成像,并以高达2.7Hz的频率对整个细胞中的线粒体和内质网动态进行成像。据我们所知,这代表了迄今为止最快的全细胞SIM成像。

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