Preparation of filamentous proteins for electron microscopy visualization and reconstruction.
Cryo-EM
Filaments
Fusion tags
Negative stain EM
Sample preparation
Journal
Methods in enzymology
ISSN: 1557-7988
Titre abrégé: Methods Enzymol
Pays: United States
ID NLM: 0212271
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
29
8
2019
pubmed:
29
8
2019
medline:
9
6
2020
Statut:
ppublish
Résumé
Cryo electron microscopy (cryo-EM) has become a mainstream tool for determining the structures of macromolecular complexes at the atomic resolution. It has many advantages over other techniques such as X-ray crystallography and nuclear magnetic resonance (NMR). However, it also entails several challenges, a major one being preparation of an ideal sample. Recent studies have identified that DNA sensors and inflammasomes often assemble into filamentous oligomers, which poses a unique set of challenges in preparing ideal samples for high-resolution reconstruction using cryo-EM. This chapter will discuss how to overcome several major issues in cryo-EM sample preparation including construct design, screening using negative stain (ns) EM, and tips on working with filamentous proteins.
Identifiants
pubmed: 31455526
pii: S0076-6879(19)30246-0
doi: 10.1016/bs.mie.2019.06.007
pii:
doi:
Substances chimiques
Macromolecular Substances
0
Proteins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
167-176Subventions
Organisme : NIGMS NIH HHS
ID : R01 GM129342
Pays : United States
Informations de copyright
© 2019 Elsevier Inc. All rights reserved.