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Single particle electron microscopy

Electron microscopy (EM) in combination with image analysis is a powerful technique to study protein structures at low, medium, and high resolution. Since electron micrographs of biological objects are very noisy, improvement of the signal-to-noise ratio by image processing is an integral part of EM...

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Detalles Bibliográficos
Autores principales: Boekema, Egbert J., Folea, Mihaela, Kouřil, Roman
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777225/
https://www.ncbi.nlm.nih.gov/pubmed/19513809
http://dx.doi.org/10.1007/s11120-009-9443-1
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author Boekema, Egbert J.
Folea, Mihaela
Kouřil, Roman
author_facet Boekema, Egbert J.
Folea, Mihaela
Kouřil, Roman
author_sort Boekema, Egbert J.
collection PubMed
description Electron microscopy (EM) in combination with image analysis is a powerful technique to study protein structures at low, medium, and high resolution. Since electron micrographs of biological objects are very noisy, improvement of the signal-to-noise ratio by image processing is an integral part of EM, and this is performed by averaging large numbers of individual projections. Averaging procedures can be divided into crystallographic and non-crystallographic methods. The crystallographic averaging method, based on two-dimensional (2D) crystals of (membrane) proteins, yielded in solving atomic protein structures in the last century. More recently, single particle analysis could be extended to solve atomic structures as well. It is a suitable method for large proteins, viruses, and proteins that are difficult to crystallize. Because it is also a fast method to reveal the low-to-medium resolution structures, the impact of its application is growing rapidly. Technical aspects, results, and possibilities are presented.
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spelling pubmed-27772252009-11-17 Single particle electron microscopy Boekema, Egbert J. Folea, Mihaela Kouřil, Roman Photosynth Res Review Electron microscopy (EM) in combination with image analysis is a powerful technique to study protein structures at low, medium, and high resolution. Since electron micrographs of biological objects are very noisy, improvement of the signal-to-noise ratio by image processing is an integral part of EM, and this is performed by averaging large numbers of individual projections. Averaging procedures can be divided into crystallographic and non-crystallographic methods. The crystallographic averaging method, based on two-dimensional (2D) crystals of (membrane) proteins, yielded in solving atomic protein structures in the last century. More recently, single particle analysis could be extended to solve atomic structures as well. It is a suitable method for large proteins, viruses, and proteins that are difficult to crystallize. Because it is also a fast method to reveal the low-to-medium resolution structures, the impact of its application is growing rapidly. Technical aspects, results, and possibilities are presented. Springer Netherlands 2009-06-10 2009 /pmc/articles/PMC2777225/ /pubmed/19513809 http://dx.doi.org/10.1007/s11120-009-9443-1 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Review
Boekema, Egbert J.
Folea, Mihaela
Kouřil, Roman
Single particle electron microscopy
title Single particle electron microscopy
title_full Single particle electron microscopy
title_fullStr Single particle electron microscopy
title_full_unstemmed Single particle electron microscopy
title_short Single particle electron microscopy
title_sort single particle electron microscopy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777225/
https://www.ncbi.nlm.nih.gov/pubmed/19513809
http://dx.doi.org/10.1007/s11120-009-9443-1
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