Virtual nanoscopy: Generation of ultra-large high resolution electron microscopy maps

被引:108
作者
Faas, Frank G. A. [1 ]
Avramut, M. Cristina [1 ]
van den Berg, Bernard M. [2 ]
Mommaas, A. Mieke [1 ]
Koster, Abraham J. [1 ]
Ravelli, Raimond B. G. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Mol Cell Biol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Nephrol, NL-2300 RC Leiden, Netherlands
关键词
CRYOELECTRON TOMOGRAPHY; CORRELATIVE MICROSCOPY; ENDOPLASMIC-RETICULUM; LIGHT-MICROSCOPY; CELL BIOLOGY; AUTOPHAGY; MEMBRANE; MITOCHONDRIA; FLUORESCENCE; COMPARTMENTS;
D O I
10.1083/jcb.201201140
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A key obstacle in uncovering the orchestration between molecular and cellular events is the vastly different length scales on which they occur. We describe here a methodology for ultrastructurally mapping regions of cells and tissue as large as 1 mm(2) at nanometer resolution. Our approach employs standard transmission electron microscopy, rapid automated data collection, and stitching to create large virtual slides. It greatly facilitates correlative light-electron microscopy studies to relate structure and function and provides a genuine representation of ultrastructural events. The method is scalable as illustrated by slides up to 281 gigapixels in size. Here, we applied virtual nanoscopy in a correlative light-electron microscopy study to address the role of the endothelial glycocalyx in protein leakage over the glomerular filtration barrier, in an immunogold labeling study of internalization of oncolytic reovirus in human dendritic cells, in a cryo-electron microscopy study of intact vitrified mouse embryonic cells, and in an ultrastructural mapping of a complete zebrafish embryo slice.
引用
收藏
页码:457 / 469
页数:13
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