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利用共聚焦激光和电子显微镜对少量单细胞真核生物进行快速特征描述的工作流程。

A rapid workflow for the characterization of small numbers of unicellular eukaryotes by using correlative light and electron microscopy.

机构信息

Institute of Immunology and Microbiology, First Faculty of Medicine, Charles University, Prague, Czech Republic.

Institute of Immunology and Microbiology, First Faculty of Medicine, Charles University, Prague, Czech Republic.

出版信息

J Microbiol Methods. 2020 May;172:105888. doi: 10.1016/j.mimet.2020.105888. Epub 2020 Mar 10.

Abstract

The limited availability of biological samples hinders phylogenetic efforts to define structural differences among various biological groups. A novel workflow enabling the analysis of protists in low cell numbers by electron microscopy (EM) is described with cysts of Giardia intestinalis, a single-celled eukaryotic parasite. Correlative light and electron microscopy (CLEM) allows for the selection of individual cells and is economical in terms of time and cost. We describe a cyst purification protocol in combination with an adhesive coating for fixation and ultrathin embedding that results in excellent preservation of cell morphology. The application of advanced structural and analytical EM methods, such as high-resolution field emission scanning electron microscopy (FESEM), focused ion beam tomography (FIB/SEM), and energy-dispersive X-ray spectroscopy (EDX) analysis, is demonstrated. The workflow represents a new approach for studying the cellular and organelle architecture of rare and "difficult to culture" microorganisms.

摘要

生物样本的有限可用性阻碍了对不同生物群体结构差异进行系统发育分析的努力。本文描述了一种通过电子显微镜(EM)分析低细胞数量原生生物的新工作流程,以肠道贾第虫的包囊为例,这是一种单细胞真核寄生虫。相关的光和电子显微镜(CLEM)允许选择单个细胞,并且在时间和成本方面具有经济性。我们描述了一种囊泡纯化方案,结合了用于固定和超薄包埋的粘附涂层,可实现出色的细胞形态保存。本文展示了高级结构和分析 EM 方法的应用,例如高分辨率场发射扫描电子显微镜(FESEM)、聚焦离子束断层扫描(FIB/SEM)和能谱分析(EDX)。该工作流程代表了一种研究稀有和“难以培养”微生物的细胞和细胞器结构的新方法。

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