Bridging structural and cell biology with cryo-electron microscopy.


Journal

Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462

Informations de publication

Date de publication:
Apr 2024
Historique:
received: 18 07 2023
accepted: 13 02 2024
medline: 4 4 2024
pubmed: 4 4 2024
entrez: 3 4 2024
Statut: ppublish

Résumé

Most life scientists would agree that understanding how cellular processes work requires structural knowledge about the macromolecules involved. For example, deciphering the double-helical nature of DNA revealed essential aspects of how genetic information is stored, copied and repaired. Yet, being reductionist in nature, structural biology requires the purification of large amounts of macromolecules, often trimmed off larger functional units. The advent of cryogenic electron microscopy (cryo-EM) greatly facilitated the study of large, functional complexes and generally of samples that are hard to express, purify and/or crystallize. Nevertheless, cryo-EM still requires purification and thus visualization outside of the natural context in which macromolecules operate and coexist. Conversely, cell biologists have been imaging cells using a number of fast-evolving techniques that keep expanding their spatial and temporal reach, but always far from the resolution at which chemistry can be understood. Thus, structural and cell biology provide complementary, yet unconnected visions of the inner workings of cells. Here we discuss how the interplay between cryo-EM and cryo-electron tomography, as a connecting bridge to visualize macromolecules in situ, holds great promise to create comprehensive structural depictions of macromolecules as they interact in complex mixtures or, ultimately, inside the cell itself.

Identifiants

pubmed: 38570716
doi: 10.1038/s41586-024-07198-2
pii: 10.1038/s41586-024-07198-2
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

47-56

Informations de copyright

© 2024. Springer Nature Limited.

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Auteurs

Eva Nogales (E)

Molecular and Cell Biology Department, Institute for Quantitative Biomedicine, University of California, Berkeley, CA, USA. enogales@lbl.gov.
Molecular Biophysics and Integrated Bioimaging, Lawrence Berkeley National Laboratory, Berkeley, CA, USA. enogales@lbl.gov.
Howard Hughes Medical Institute, Berkeley, CA, USA. enogales@lbl.gov.

Julia Mahamid (J)

Structural and Computational Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany. julia.mahamid@embl.de.
Cell Biology and Biophysics Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany. julia.mahamid@embl.de.

Classifications MeSH