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ColorEM:用于元素引导的生命基本组成部分识别与成像的分析电子显微镜。

ColorEM: analytical electron microscopy for element-guided identification and imaging of the building blocks of life.

作者信息

Pirozzi Nicole M, Hoogenboom Jacob P, Giepmans Ben N G

机构信息

Department of Cell Biology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Department of Imaging Physics, Delft University of Technology, Delft, The Netherlands.

出版信息

Histochem Cell Biol. 2018 Nov;150(5):509-520. doi: 10.1007/s00418-018-1707-4. Epub 2018 Aug 17.

DOI:10.1007/s00418-018-1707-4
PMID:30120552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6182685/
Abstract

Nanometer-scale identification of multiple targets is crucial to understand how biomolecules regulate life. Markers, or probes, of specific biomolecules help to visualize and to identify. Electron microscopy (EM), the highest resolution imaging modality, provides ultrastructural information where several subcellular structures can be readily identified. For precise tagging of (macro)molecules, electron-dense probes, distinguishable in gray-scale EM, are being used. However, practically these genetically-encoded or immune-targeted probes are limited to three targets. In correlated microscopy, fluorescent signals are overlaid on the EM image, but typically without the nanometer-scale resolution and limited to visualization of few targets. Recently, analytical methods have become more sensitive, which has led to a renewed interest to explore these for imaging of elements and molecules in cells and tissues in EM. Here, we present the current state of nanoscale imaging of cells and tissues using energy dispersive X-ray analysis (EDX), electron energy loss spectroscopy (EELS), cathodoluminescence (CL), and touch upon secondary ion mass spectroscopy at the nanoscale (NanoSIMS). ColorEM is the term encompassing these analytical techniques the results of which are then displayed as false-color at the EM scale. We highlight how ColorEM will become a strong analytical nano-imaging tool in life science microscopy.

摘要

对多个目标进行纳米级识别对于理解生物分子如何调节生命至关重要。特定生物分子的标记物或探针有助于可视化和识别。电子显微镜(EM)是分辨率最高的成像方式,可提供超微结构信息,通过它可以轻松识别几种亚细胞结构。为了对(大)分子进行精确标记,人们正在使用在灰度EM中可区分的电子致密探针。然而,实际上,这些基因编码或免疫靶向的探针仅限于三个目标。在相关显微镜中,荧光信号叠加在EM图像上,但通常没有纳米级分辨率,并且仅限于少数目标的可视化。最近,分析方法变得更加灵敏,这引发了人们重新探索这些方法用于在EM中对细胞和组织中的元素和分子进行成像的兴趣。在这里,我们介绍了使用能量色散X射线分析(EDX)、电子能量损失谱(EELS)、阴极发光(CL)以及涉及纳米级二次离子质谱(NanoSIMS)对细胞和组织进行纳米级成像的现状。ColorEM是一个涵盖这些分析技术的术语,其结果随后在EM尺度上显示为假彩色。我们强调ColorEM将如何成为生命科学显微镜中一种强大的分析纳米成像工具。

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