| Literature DB >> 28559166 |
Jie He1, Chyongere Hsieh1, Yongping Wu2, Thomas Schmelzer3, Pan Wang4, Ying Lin4, Michael Marko1, Haixin Sui5.
Abstract
Cryo-electron tomography (cryo-ET) is a well-established technique for studying 3D structural details of subcellular macromolecular complexes and organelles in their nearly native context in the cell. A primary limitation of the application of cryo-ET is the accessible specimen thickness, which is less than the diameters of almost all eukaryotic cells. It has been shown that focused ion beam (FIB) milling can be used to prepare thin, distortion-free lamellae of frozen biological material for high-resolution cryo-ET. Commercial cryosystems are available for cryo-FIB specimen preparation, however re-engineering and additional fixtures are often essential for reliable results with a particular cryo-FIB and cryo-transmission electron microscope (cryo-TEM). Here, we describe our optimized protocol and modified instrumentation for cryo-FIB milling to produce thin lamellae and subsequent damage-free cryotransfer of the lamellae into our cartridge-type cryo-TEM. Published by Elsevier Inc.Entities:
Keywords: Alcohol-oxidase; Cryo-ET; Cryo-FIB; Organelles; TEM cartridges; Yeast
Mesh:
Year: 2017 PMID: 28559166 PMCID: PMC5555045 DOI: 10.1016/j.jsb.2017.05.011
Source DB: PubMed Journal: J Struct Biol ISSN: 1047-8477 Impact factor: 2.867