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Electron-counting MicroED data with the K2 and K3 direct electron detectors

Microcrystal electron diffraction (MicroED) uses electron cryo-microscopy (cryo-EM) to collect diffraction data from small crystals during continuous rotation of the sample. As a result of advances in hardware as well as methods development, the data quality has continuously improved over the past d...

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Autores principales: Clabbers, Max T.B., Martynowycz, Michael W., Hattne, Johan, Nannenga, Brent L., Gonen, Tamir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9999727/
https://www.ncbi.nlm.nih.gov/pubmed/36044956
http://dx.doi.org/10.1016/j.jsb.2022.107886
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author Clabbers, Max T.B.
Martynowycz, Michael W.
Hattne, Johan
Nannenga, Brent L.
Gonen, Tamir
author_facet Clabbers, Max T.B.
Martynowycz, Michael W.
Hattne, Johan
Nannenga, Brent L.
Gonen, Tamir
author_sort Clabbers, Max T.B.
collection PubMed
description Microcrystal electron diffraction (MicroED) uses electron cryo-microscopy (cryo-EM) to collect diffraction data from small crystals during continuous rotation of the sample. As a result of advances in hardware as well as methods development, the data quality has continuously improved over the past decade, to the point where even macromolecular structures can be determined ab initio. Detectors suitable for electron diffraction should ideally have fast readout to record data in movie mode, and high sensitivity at low exposure rates to accurately report the intensities. Direct electron detectors are commonly used in cryo-EM imaging for their sensitivity and speed, but despite their availability are generally not used in diffraction. Primary concerns with diffraction experiments are the dynamic range and coincidence loss, which will corrupt the measurement if the flux exceeds the count rate of the detector. Here, we describe instrument setup and low-exposure MicroED data collection in electron-counting mode using K2 and K3 direct electron detectors and show that the integrated intensities can be effectively used to solve structures of two macromolecules between 1.2 Å and 2.8 Å resolution. Even though a beam stop was not used with the K3 studies we did not observe damage to the camera. As these cameras are already available in many cryo-EM facilities, this provides opportunities for users who do not have access to dedicated facilities for MicroED.
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spelling pubmed-99997272023-03-10 Electron-counting MicroED data with the K2 and K3 direct electron detectors Clabbers, Max T.B. Martynowycz, Michael W. Hattne, Johan Nannenga, Brent L. Gonen, Tamir J Struct Biol Article Microcrystal electron diffraction (MicroED) uses electron cryo-microscopy (cryo-EM) to collect diffraction data from small crystals during continuous rotation of the sample. As a result of advances in hardware as well as methods development, the data quality has continuously improved over the past decade, to the point where even macromolecular structures can be determined ab initio. Detectors suitable for electron diffraction should ideally have fast readout to record data in movie mode, and high sensitivity at low exposure rates to accurately report the intensities. Direct electron detectors are commonly used in cryo-EM imaging for their sensitivity and speed, but despite their availability are generally not used in diffraction. Primary concerns with diffraction experiments are the dynamic range and coincidence loss, which will corrupt the measurement if the flux exceeds the count rate of the detector. Here, we describe instrument setup and low-exposure MicroED data collection in electron-counting mode using K2 and K3 direct electron detectors and show that the integrated intensities can be effectively used to solve structures of two macromolecules between 1.2 Å and 2.8 Å resolution. Even though a beam stop was not used with the K3 studies we did not observe damage to the camera. As these cameras are already available in many cryo-EM facilities, this provides opportunities for users who do not have access to dedicated facilities for MicroED. 2022-12 2022-08-28 /pmc/articles/PMC9999727/ /pubmed/36044956 http://dx.doi.org/10.1016/j.jsb.2022.107886 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Clabbers, Max T.B.
Martynowycz, Michael W.
Hattne, Johan
Nannenga, Brent L.
Gonen, Tamir
Electron-counting MicroED data with the K2 and K3 direct electron detectors
title Electron-counting MicroED data with the K2 and K3 direct electron detectors
title_full Electron-counting MicroED data with the K2 and K3 direct electron detectors
title_fullStr Electron-counting MicroED data with the K2 and K3 direct electron detectors
title_full_unstemmed Electron-counting MicroED data with the K2 and K3 direct electron detectors
title_short Electron-counting MicroED data with the K2 and K3 direct electron detectors
title_sort electron-counting microed data with the k2 and k3 direct electron detectors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9999727/
https://www.ncbi.nlm.nih.gov/pubmed/36044956
http://dx.doi.org/10.1016/j.jsb.2022.107886
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