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Combining X-Ray Crystallography and Electron Microscopy

The combination of cryo-electron microscopy to study large biological assemblies at low resolution with crystallography to determine near atomic structures of assembly fragments is quickly expanding the horizon of structural biology. This technique can be used to advantage in the study of large stru...

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Detalles Bibliográficos
Autores principales: Rossmann, Michael G., Morais, Marc C., Leiman, Petr G., Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173138/
https://www.ncbi.nlm.nih.gov/pubmed/15766536
http://dx.doi.org/10.1016/j.str.2005.01.005
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author Rossmann, Michael G.
Morais, Marc C.
Leiman, Petr G.
Zhang, Wei
author_facet Rossmann, Michael G.
Morais, Marc C.
Leiman, Petr G.
Zhang, Wei
author_sort Rossmann, Michael G.
collection PubMed
description The combination of cryo-electron microscopy to study large biological assemblies at low resolution with crystallography to determine near atomic structures of assembly fragments is quickly expanding the horizon of structural biology. This technique can be used to advantage in the study of large structures that cannot be crystallized, to follow dynamic processes, and to “purify” samples by visual selection of particles. Factors affecting the quality of cryo-electron microscopy maps and limits of accuracy in fitting known structural fragments are discussed.
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spelling pubmed-71731382020-04-22 Combining X-Ray Crystallography and Electron Microscopy Rossmann, Michael G. Morais, Marc C. Leiman, Petr G. Zhang, Wei Structure Review The combination of cryo-electron microscopy to study large biological assemblies at low resolution with crystallography to determine near atomic structures of assembly fragments is quickly expanding the horizon of structural biology. This technique can be used to advantage in the study of large structures that cannot be crystallized, to follow dynamic processes, and to “purify” samples by visual selection of particles. Factors affecting the quality of cryo-electron microscopy maps and limits of accuracy in fitting known structural fragments are discussed. Elsevier Ltd. 2005-03 2005-03-09 /pmc/articles/PMC7173138/ /pubmed/15766536 http://dx.doi.org/10.1016/j.str.2005.01.005 Text en Copyright © 2005 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review
Rossmann, Michael G.
Morais, Marc C.
Leiman, Petr G.
Zhang, Wei
Combining X-Ray Crystallography and Electron Microscopy
title Combining X-Ray Crystallography and Electron Microscopy
title_full Combining X-Ray Crystallography and Electron Microscopy
title_fullStr Combining X-Ray Crystallography and Electron Microscopy
title_full_unstemmed Combining X-Ray Crystallography and Electron Microscopy
title_short Combining X-Ray Crystallography and Electron Microscopy
title_sort combining x-ray crystallography and electron microscopy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173138/
https://www.ncbi.nlm.nih.gov/pubmed/15766536
http://dx.doi.org/10.1016/j.str.2005.01.005
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