Single-Particle Cryo-EM Data Collection with Stage Tilt using Leginon.


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:
01 07 2022
Historique:
entrez: 18 7 2022
pubmed: 19 7 2022
medline: 22 7 2022
Statut: epublish

Résumé

Single-particle analysis (SPA) by cryo-electron microscopy (cryo-EM) is now a mainstream technique for high-resolution structural biology. Structure determination by SPA relies upon obtaining multiple distinct views of a macromolecular object vitrified within a thin layer of ice. Ideally, a collection of uniformly distributed random projection orientations would amount to all possible views of the object, giving rise to reconstructions characterized by isotropic directional resolution. However, in reality, many samples suffer from preferentially oriented particles adhering to the air-water interface. This leads to non-uniform angular orientation distributions in the dataset and inhomogeneous Fourier-space sampling in the reconstruction, translating into maps characterized by anisotropic resolution. Tilting the specimen stage provides a generalizable solution to overcoming resolution anisotropy by virtue of improving the uniformity of orientation distributions, and thus the isotropy of Fourier space sampling. The present protocol describes a tilted-stage automated data collection strategy using Leginon, a software for automated image acquisition. The procedure is simple to implement, does not require any additional equipment or software, and is compatible with most standard transmission electron microscopes (TEMs) used for imaging biological macromolecules.

Identifiants

pubmed: 35848829
doi: 10.3791/64136
pmc: PMC9733953
mid: NIHMS1846518
doi:

Substances chimiques

Macromolecular Substances 0

Types de publication

Journal Article Video-Audio Media Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI136680
Pays : United States
Organisme : NIGMS NIH HHS
ID : F32 GM148049
Pays : United States
Organisme : NIAID NIH HHS
ID : U54 AI170855
Pays : United States
Organisme : NIAID NIH HHS
ID : U54 AI150472
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI136680
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA014195
Pays : United States

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Auteurs

Sriram Aiyer (S)

Laboratory of Genetics, The Salk Institute for Biological Studies.

Timothy S Strutzenberg (TS)

Laboratory of Genetics, The Salk Institute for Biological Studies.

Marianne E Bowman (ME)

Jack H. Skirball Center for Chemical Biology and Proteomics, The Salk Institute for Biological Studies.

Joseph P Noel (JP)

Jack H. Skirball Center for Chemical Biology and Proteomics, The Salk Institute for Biological Studies; Department of Chemistry and Biochemistry, University of California San Diego.

Dmitry Lyumkis (D)

Laboratory of Genetics, The Salk Institute for Biological Studies; Graduate School of Biological Sciences, Section of Molecular Biology, University of California San Diego; Department of Integrative Structural and Computational Biology, The Scripps Research Institute; dlyumkis@salk.edu.

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Classifications MeSH