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An introduction to sample preparation and imaging by cryo-electron microscopy for structural biology

Transmission electron microscopy (EM) is a versatile technique that can be used to image biological specimens ranging from intact eukaryotic cells to individual proteins >150 kDa. There are several strategies for preparing samples for imaging by EM, including negative staining and cryogenic freez...

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Detalles Bibliográficos
Autores principales: Thompson, Rebecca F., Walker, Matt, Siebert, C. Alistair, Muench, Stephen P., Ranson, Neil A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854231/
https://www.ncbi.nlm.nih.gov/pubmed/26931652
http://dx.doi.org/10.1016/j.ymeth.2016.02.017
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author Thompson, Rebecca F.
Walker, Matt
Siebert, C. Alistair
Muench, Stephen P.
Ranson, Neil A.
author_facet Thompson, Rebecca F.
Walker, Matt
Siebert, C. Alistair
Muench, Stephen P.
Ranson, Neil A.
author_sort Thompson, Rebecca F.
collection PubMed
description Transmission electron microscopy (EM) is a versatile technique that can be used to image biological specimens ranging from intact eukaryotic cells to individual proteins >150 kDa. There are several strategies for preparing samples for imaging by EM, including negative staining and cryogenic freezing. In the last few years, cryo-EM has undergone a ‘resolution revolution’, owing to both advances in imaging hardware, image processing software, and improvements in sample preparation, leading to growing number of researchers using cryo-EM as a research tool. However, cryo-EM is still a rapidly growing field, with unique challenges. Here, we summarise considerations for imaging of a range of specimens from macromolecular complexes to cells using EM.
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spelling pubmed-48542312016-05-10 An introduction to sample preparation and imaging by cryo-electron microscopy for structural biology Thompson, Rebecca F. Walker, Matt Siebert, C. Alistair Muench, Stephen P. Ranson, Neil A. Methods Article Transmission electron microscopy (EM) is a versatile technique that can be used to image biological specimens ranging from intact eukaryotic cells to individual proteins >150 kDa. There are several strategies for preparing samples for imaging by EM, including negative staining and cryogenic freezing. In the last few years, cryo-EM has undergone a ‘resolution revolution’, owing to both advances in imaging hardware, image processing software, and improvements in sample preparation, leading to growing number of researchers using cryo-EM as a research tool. However, cryo-EM is still a rapidly growing field, with unique challenges. Here, we summarise considerations for imaging of a range of specimens from macromolecular complexes to cells using EM. Academic Press 2016-05-01 /pmc/articles/PMC4854231/ /pubmed/26931652 http://dx.doi.org/10.1016/j.ymeth.2016.02.017 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Thompson, Rebecca F.
Walker, Matt
Siebert, C. Alistair
Muench, Stephen P.
Ranson, Neil A.
An introduction to sample preparation and imaging by cryo-electron microscopy for structural biology
title An introduction to sample preparation and imaging by cryo-electron microscopy for structural biology
title_full An introduction to sample preparation and imaging by cryo-electron microscopy for structural biology
title_fullStr An introduction to sample preparation and imaging by cryo-electron microscopy for structural biology
title_full_unstemmed An introduction to sample preparation and imaging by cryo-electron microscopy for structural biology
title_short An introduction to sample preparation and imaging by cryo-electron microscopy for structural biology
title_sort introduction to sample preparation and imaging by cryo-electron microscopy for structural biology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854231/
https://www.ncbi.nlm.nih.gov/pubmed/26931652
http://dx.doi.org/10.1016/j.ymeth.2016.02.017
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