| Literature DB >> 27432264 |
Benjamin Titze1, Christel Genoud2.
Abstract
Electron microscopy (EM) has been a key imaging method to investigate biological ultrastructure for over six decades. In recent years, novel volume EM techniques have significantly advanced nanometre-scale imaging of cells and tissues in three dimensions. Previously, this had depended on the slow and error-prone manual tasks of cutting and handling large numbers of sections, and imaging them one-by-one with transmission EM. Now, automated volume imaging methods mostly based on scanning EM (SEM) allow faster and more reliable acquisition of serial images through tissue volumes and achieve higher z-resolution. Various software tools have been developed to manipulate the acquired image stacks and facilitate quantitative analysis. Here, we introduce three volume SEM methods: serial block-face electron microscopy (SBEM), focused ion beam SEM (FIB-SEM) and automated tape-collecting ultramicrotome SEM (ATUM-SEM). We discuss and compare their capabilities, provide an overview of the full volume SEM workflow for obtaining 3D datasets and showcase different applications for biological research.Keywords: Brain/nervous system; Cellular imaging; Electron microscopy; Systems biology
Mesh:
Year: 2016 PMID: 27432264 DOI: 10.1111/boc.201600024
Source DB: PubMed Journal: Biol Cell ISSN: 0248-4900 Impact factor: 4.458