Combining Metabolic Pulse Labeling and Quantitative Proteomics to Monitor Protein Synthesis Upon Viral Infection.

BONCAT Influenza A virus Orthogonal labeling Quantitative proteomics Shutoff Species barrier Translation

Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2023
Historique:
entrez: 19 12 2022
pubmed: 20 12 2022
medline: 22 12 2022
Statut: ppublish

Résumé

Viruses like influenza A virus (IAV) hijack host cells in order to replicate. To actively and abundantly synthesize viral proteins, they reprogram the cellular transcriptional and translational landscape. Here, we present a proteomic approach that allows us to quantify the differences in host and viral protein synthesis comparatively for different strains of IAV. The method is based on combining quantitative proteomics using stable isotope labelling by amino acids in cell culture (SILAC) and bioorthogonal labeling with methionine analogs. This methodology accurately quantifies synthesis of host and viral proteins with high temporal resolution and faithfully detects global changes in cellular translation capacity. It thus provides unique insights into the dynamics of protein synthesis as the infection progresses.

Identifiants

pubmed: 36534289
doi: 10.1007/978-1-0716-2895-9_13
doi:

Substances chimiques

Viral Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

149-165

Informations de copyright

© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Boris Bogdanow (B)

Research group "Structural Interactomics", Department of Structural Biology, Leibniz-Institute for Molecular Pharmacology, Berlin, Germany. bogdanow@fmp-berlin.de.

Niki Katsimani (N)

Research group "Structural Interactomics", Department of Structural Biology, Leibniz-Institute for Molecular Pharmacology, Berlin, Germany.

Fan Liu (F)

Research group "Structural Interactomics", Department of Structural Biology, Leibniz-Institute for Molecular Pharmacology, Berlin, Germany.

Matthias Selbach (M)

Research group "Proteome Dynamics", Max-Delbrück Center for Molecular Medicine, Berlin, Germany.

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