The Evolution and the Advantages of MicroED
MicroED is a method which combines cryo-EM sample preparation and instrumentation, with electron and X-ray crystallography data analysis, and it has been employed to solve many protein crystal structures at high resolution. Initially, the main doubts of this method for structure determination were t...
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doaj-7d826fbad97245268e720191c02687312020-11-24T21:26:49ZengFrontiers Media S.A.Frontiers in Molecular Biosciences2296-889X2018-12-01510.3389/fmolb.2018.00114413867The Evolution and the Advantages of MicroEDBrent L. Nannenga0Guanhong Bu1Dan Shi2School for Engineering of Matter, Transport and Energy, Arizona State University, Tempe, AZ, United StatesSchool for Engineering of Matter, Transport and Energy, Arizona State University, Tempe, AZ, United StatesStructural Biophysics Laboratory, National Frederick Laboratory for Cancer Research, National Cancer Institute, Frederick, MD, United StatesMicroED is a method which combines cryo-EM sample preparation and instrumentation, with electron and X-ray crystallography data analysis, and it has been employed to solve many protein crystal structures at high resolution. Initially, the main doubts of this method for structure determination were the dynamic scattering of electrons, which would cause severe inaccuracies in the measured intensities. In this paper, we will review the evolution of MicroED data collection and processing, the major differences of multiple scattering effects in protein crystals and inorganic material, and the advantages of continuous rotation data collection. Additionally, because of the periodic nature of the crystalline sample, radiation doses can be kept significantly lower than those used in single particle data collection. We review the work where this was used to assess the radiation damage of a high-energy electron beam on the protein molecules at much lower dose ranges compared to imaging.https://www.frontiersin.org/article/10.3389/fmolb.2018.00114/fullCryo-EMcrystallographyMicroEDdynamic scatteringradiation damage |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Brent L. Nannenga Guanhong Bu Dan Shi |
spellingShingle |
Brent L. Nannenga Guanhong Bu Dan Shi The Evolution and the Advantages of MicroED Frontiers in Molecular Biosciences Cryo-EM crystallography MicroED dynamic scattering radiation damage |
author_facet |
Brent L. Nannenga Guanhong Bu Dan Shi |
author_sort |
Brent L. Nannenga |
title |
The Evolution and the Advantages of MicroED |
title_short |
The Evolution and the Advantages of MicroED |
title_full |
The Evolution and the Advantages of MicroED |
title_fullStr |
The Evolution and the Advantages of MicroED |
title_full_unstemmed |
The Evolution and the Advantages of MicroED |
title_sort |
evolution and the advantages of microed |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Molecular Biosciences |
issn |
2296-889X |
publishDate |
2018-12-01 |
description |
MicroED is a method which combines cryo-EM sample preparation and instrumentation, with electron and X-ray crystallography data analysis, and it has been employed to solve many protein crystal structures at high resolution. Initially, the main doubts of this method for structure determination were the dynamic scattering of electrons, which would cause severe inaccuracies in the measured intensities. In this paper, we will review the evolution of MicroED data collection and processing, the major differences of multiple scattering effects in protein crystals and inorganic material, and the advantages of continuous rotation data collection. Additionally, because of the periodic nature of the crystalline sample, radiation doses can be kept significantly lower than those used in single particle data collection. We review the work where this was used to assess the radiation damage of a high-energy electron beam on the protein molecules at much lower dose ranges compared to imaging. |
topic |
Cryo-EM crystallography MicroED dynamic scattering radiation damage |
url |
https://www.frontiersin.org/article/10.3389/fmolb.2018.00114/full |
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