Strategies for Optimization of Cryogenic Electron Tomography Data Acquisition.


Journal

Journal of visualized experiments : JoVE
ISSN: 1940-087X
Titre abrégé: J Vis Exp
Pays: United States
ID NLM: 101313252

Informations de publication

Date de publication:
19 03 2021
Historique:
entrez: 5 4 2021
pubmed: 6 4 2021
medline: 13 4 2021
Statut: epublish

Résumé

Cryogenic electron tomography (cryoET) is a powerful method to study the 3D structure of biological samples in a close-to-native state. Current state-of-the-art cryoET combined with subtomogram averaging analysis enables the high-resolution structural determination of macromolecular complexes that are present in multiple copies within tomographic reconstructions. Tomographic experiments usually require a vast amount of tilt series to be acquired by means of high-end transmission electron microscopes with important operational running-costs. Although the throughput and reliability of automated data acquisition routines have constantly improved over the recent years, the process of selecting regions of interest at which a tilt series will be acquired cannot be easily automated and it still relies on the user's manual input. Therefore, the set-up of a large-scale data collection session is a time-consuming procedure that can considerably reduce the remaining microscope time available for tilt series acquisition. Here, the protocol describes the recently developed implementations based on the SerialEM package and the PyEM software that significantly improve the time-efficiency of grid screening and large-scale tilt series data collection. The presented protocol illustrates how to use SerialEM scripting functionalities to fully automate grid mapping, grid square mapping, and tilt series acquisition. Furthermore, the protocol describes how to use PyEM to select additional acquisition targets in off-line mode after automated data collection is initiated. To illustrate this protocol, its application in the context of high-end data collection of Sars-Cov-2 tilt series is described. The presented pipeline is particularly suited to maximizing the time-efficiency of tomography experiments that require a careful selection of acquisition targets and at the same time a large amount of tilt series to be collected.

Identifiants

pubmed: 33818563
doi: 10.3791/62383
doi:

Substances chimiques

Macromolecular Substances 0

Types de publication

Journal Article Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Felix Weis (F)

Structural and Computational Biology Unit, European Molecular Biology Laboratory.

Wim J H Hagen (WJH)

Structural and Computational Biology Unit, European Molecular Biology Laboratory.

Martin Schorb (M)

Electron Microscopy Core Facility, European Molecular Biology Laboratory.

Simone Mattei (S)

Structural and Computational Biology Unit, European Molecular Biology Laboratory; Imaging Centre, European Molecular Biology Laboratory; simone.mattei@embl.de.

Articles similaires

Selecting optimal software code descriptors-The case of Java.

Yegor Bugayenko, Zamira Kholmatova, Artem Kruglov et al.
1.00
Software Algorithms Programming Languages
Photosynthesis Ribulose-Bisphosphate Carboxylase Carbon Dioxide Molecular Dynamics Simulation Cyanobacteria
Humans Multiple Myeloma Male Aged Glomerulosclerosis, Focal Segmental

Classifications MeSH