Projective oblique plane structured illumination microscopy

Bo-Jui Chang, Douglas Shepherd, Reto Fiolka
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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.

Abstract Image

投射斜面结构照明显微镜
结构照明显微镜(SIM)可将荧光显微镜的空间分辨率提高一倍,二维格式的视频速率活细胞成像也已得到证实。然而,二维结构照明显微镜的快速实施通常只能覆盖紧贴盖玻片的狭小样本切片,大部分细胞体积无法触及。在这里,我们采用投影形式的斜面结构照明显微镜(OPSIM),在二维 SIM 框架内对整个细胞进行快速成像。由于不涉及样品或物镜的机械扫描,该技术具有快速投影成像和加倍分辨率的潜力。我们用荧光纳米球鉴定了空间分辨率,比较了使用 OPSIM 的投影和三维成像,并以高达 2.7 Hz 的速度对整个细胞的线粒体和 ER 动态进行了成像。据我们所知,这是迄今为止最快的全细胞 SIM 成像。
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