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利用 VividSTORM 进行相关共聚焦和超分辨率成像。

Correlated confocal and super-resolution imaging by VividSTORM.

机构信息

Momentum Laboratory of Molecular Neurobiology, Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.

School of Ph.D. Studies, Semmelweis University, Budapest, Hungary.

出版信息

Nat Protoc. 2016 Jan;11(1):163-83. doi: 10.1038/nprot.2016.002. Epub 2015 Dec 30.

Abstract

Single-molecule localization microscopy (SMLM) is rapidly gaining popularity in the life sciences as an efficient approach to visualize molecular distribution with nanoscale precision. However, it has been challenging to obtain and analyze such data within a cellular context in tissue preparations. Here we describe a 5-d tissue processing and immunostaining procedure that is optimized for SMLM, and we provide example applications to fixed mouse brain, heart and kidney tissues. We then describe how to perform correlated confocal and 3D-superresolution imaging on these sections, which allows the visualization of nanoscale protein localization within labeled subcellular compartments of identified target cells in a few minutes. Finally, we describe the use of VividSTORM (http://katonalab.hu/index.php/vividstorm), an open-source software for correlated confocal and SMLM image analysis, which facilitates the measurement of molecular abundance, clustering, internalization, surface density and intermolecular distances in a cell-specific and subcellular compartment-restricted manner. The protocol requires only basic skills in tissue staining and microscopy.

摘要

单分子定位显微镜(SMLM)作为一种在纳米尺度上可视化分子分布的有效方法,在生命科学中迅速流行起来。然而,在组织制备中,从细胞环境中获取和分析此类数据一直具有挑战性。在这里,我们描述了一种针对 SMLM 进行了优化的 5D 组织处理和免疫染色程序,并提供了固定的小鼠脑、心脏和肾脏组织的应用示例。然后,我们描述了如何对这些切片进行共聚焦和 3D 超分辨率成像,这允许在几分钟内可视化标记的亚细胞隔室内目标细胞内的纳米级蛋白质定位。最后,我们描述了使用 VividSTORM(http://katonalab.hu/index.php/vividstorm),一种用于共聚焦和 SMLM 图像分析的开源软件,该软件可以以细胞特异性和亚细胞隔室限制的方式方便地测量分子丰度、聚类、内化、表面密度和分子间距离。该方案仅需要组织染色和显微镜的基本技能。

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