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使用连续块面和聚焦离子束扫描电子显微镜的靶向研究

Targeted Studies Using Serial Block Face and Focused Ion Beam Scan Electron Microscopy.

作者信息

Guérin Christopher J, Kremer Anna, Borghgraef Peter, Lippens Saskia

机构信息

VIB Bio Imaging Core; VIB Inflammation Research Center; Department of Molecular Biomedical Research, UGent.

VIB Bio Imaging Core; VIB Inflammation Research Center; Department of Molecular Biomedical Research, UGent;

出版信息

J Vis Exp. 2019 Aug 10(150). doi: 10.3791/59480.

Abstract

This protocol allows for the efficient and effective imaging of cell or tissue samples in three dimensions at the resolution level of electron microscopy. For many years electron microscopy (EM) has remained an inherently two-dimensional technique. With the advent of serial scanning electron microscope imaging techniques (volume EM), using either an integrated microtome or focused ion beam to slice then view embedded tissues, the third dimension becomes easily accessible. Serial block face scanning electron microscopy (SBF-SEM) uses an ultramicrotome enclosed in the SEM chamber. It has the capability to handle large specimens (1,000 µm x 1,000 µm) and image large fields of view at small X,Y pixel size, but is limited in the Z dimension by the diamond knife. Focused ion beam SEM (FIB-SEM) is not limited in 3D resolution, (isotropic voxels of ≤5 nm are achievable), but the field of view is much more limited. This protocol demonstrates a workflow for combining the two techniques to allow for finding individual regions of interest (ROIs) in a large field and then imaging the subsequent targeted volume at high isotropic voxel resolution. Preparing fixed cells or tissues is more demanding for volume EM techniques due to the extra contrasting needed for efficient signal generation in SEM imaging. Such protocols are time consuming and labor intensive. This protocol also incorporates microwave assisted tissue processing facilitating the penetration of reagents, which reduces the time needed for the processing protocol from days to hours.

摘要

该方案能够以电子显微镜的分辨率水平对细胞或组织样本进行高效的三维成像。多年来,电子显微镜(EM)一直是一种固有的二维技术。随着连续扫描电子显微镜成像技术(容积电子显微镜)的出现,使用集成切片机或聚焦离子束对包埋组织进行切片然后观察,第三维变得易于获取。连续块面扫描电子显微镜(SBF-SEM)使用封闭在扫描电子显微镜腔室内的超薄切片机。它能够处理大尺寸样本(1000 µm×1000 µm),并以小的X、Y像素尺寸对大视野进行成像,但在Z维度上受金刚石刀的限制。聚焦离子束扫描电子显微镜(FIB-SEM)在三维分辨率上不受限制(可实现≤5 nm的各向同性体素),但其视野要小得多。该方案展示了一种将两种技术结合的工作流程,以便在大视野中找到单个感兴趣区域(ROI),然后以高各向同性体素分辨率对后续目标体积进行成像。由于扫描电子显微镜成像中有效信号生成需要额外的对比,对于容积电子显微镜技术来说,制备固定细胞或组织的要求更高。此类方案既耗时又费力。该方案还纳入了微波辅助组织处理,促进试剂渗透,从而将处理方案所需时间从数天缩短至数小时。

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