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Quantitative Proteomics Identified TTC4 as a TBK1 Interactor and a Positive Regulator of SeV-Induced Innate Immunity.
- Source :
-
Proteomics [Proteomics] 2018 Jan; Vol. 18 (2). - Publication Year :
- 2018
-
Abstract
- TBK1, STING, and MDA5 are important players within the antiviral innate immune response network. We mapped the interactome of endogenous TBK1, STING, and MDA5 by affinity enrichment MS in virally infected or uninfected THP-1 cells. Based on quantitative data of more than 2000 proteins and stringent statistical analysis, 58 proteins were identified as high-confidence interactors for at least one of three bait proteins. Our data indicated that TBK1 and MDA5 mostly interacted within preexisting protein networks, while STING interacted with different proteins with different viral infections. Functional analysis was performed on 17 interactors, and six were found to have functions in innate immune responses. We identified TTC4 as a TBK1 interactor and positive regulator of sendai virus-induced innate immunity.<br /> (© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)
- Subjects :
- HEK293 Cells
Humans
Macrophages immunology
Macrophages metabolism
Macrophages virology
Protein Interaction Domains and Motifs
Respirovirus Infections metabolism
Respirovirus Infections virology
Sendai virus isolation & purification
THP-1 Cells
Virus Replication
Immunity, Innate
Protein Serine-Threonine Kinases metabolism
Proteomics methods
Respirovirus Infections immunology
Sendai virus physiology
Tumor Suppressor Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1615-9861
- Volume :
- 18
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Proteomics
- Publication Type :
- Academic Journal
- Accession number :
- 29251827
- Full Text :
- https://doi.org/10.1002/pmic.201700403