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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...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Springer Netherlands
2009
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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. |
format | Text |
id | pubmed-2777225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT boekemaegbertj singleparticleelectronmicroscopy AT foleamihaela singleparticleelectronmicroscopy AT kourilroman singleparticleelectronmicroscopy |