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About:
Phosphoproteomic-based kinase profiling early in influenza virus infection identifies GRK2 as antiviral drug target
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Phosphoproteomic-based kinase profiling early in influenza virus infection identifies GRK2 as antiviral drug target
Creator
Dijkman, Ronald
Schmolke, Mirco
Yángüez, Emilio
Elshina, Elizaveta
Gehrig, Peter
Grossmann, Jonas
Hunziker, Annika
Karakus, Umut
Schading, Simon
Stertz, Silke
Yildiz, Soner
Dobay, Maria
Source
PMC
abstract
Although annual influenza epidemics affect around 10% of the global population, current treatment options are limited and development of new antivirals is needed. Here, using quantitative phosphoproteomics, we reveal the unique phosphoproteome dynamics that occur in the host cell within minutes of influenza A virus (IAV) infection. We uncover cellular kinases required for the observed signaling pattern and find that inhibition of selected candidates, such as the G protein-coupled receptor kinase 2 (GRK2), leads to decreased IAV replication. As GRK2 has emerged as drug target in heart disease, we focus on its role in IAV infection and show that it is required for viral uncoating. Replication of seasonal and pandemic IAVs is severely decreased by specific GRK2 inhibitors in primary human airway cultures and in mice. Our study reveals the IAV-induced changes to the cellular phosphoproteome and identifies GRK2 as crucial node of the kinase network that enables IAV replication.
has issue date
2018-09-11
(
xsd:dateTime
)
bibo:doi
10.1038/s41467-018-06119-y
bibo:pmid
30206219
has license
cc-by
sha1sum (hex)
554d4209692f1b384ec738f3c74b110ccf5e8dbb
schema:url
https://doi.org/10.1038/s41467-018-06119-y
resource representing a document's title
Phosphoproteomic-based kinase profiling early in influenza virus infection identifies GRK2 as antiviral drug target
has PubMed Central identifier
PMC6133941
has PubMed identifier
30206219
schema:publication
Nat Commun
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covid:554d4209692f1b384ec738f3c74b110ccf5e8dbb#body_text
is
schema:about
of
named entity 'cellular'
named entity 'host'
named entity 'kinase'
named entity 'antiviral drug'
named entity 'EARLY'
named entity 'DRUG TARGET'
named entity 'HEART DISEASE'
named entity 'G PROTEIN-COUPLED RECEPTOR KINASE 2'
named entity 'PRIMARY'
named entity 'AIRWAY'
named entity '10%'
named entity 'STUDY'
named entity 'DEVELOPMENT'
named entity 'INFLUENZA A VIRUS'
named entity 'MINUTES'
named entity 'KINASE'
named entity 'ANTIVIRALS'
named entity 'QUANTITATIVE'
named entity 'INHIBITORS'
named entity 'HERE'
named entity 'INHIBITION'
named entity 'REVEAL'
named entity 'GRK2'
named entity 'DYNAMICS'
named entity 'VIRAL UNCOATING'
named entity 'DRUG TARGET'
named entity 'REQUIRED'
named entity 'INFECTION'
named entity 'LIMITED'
named entity 'OUR'
named entity 'EPIDEMICS'
named entity 'HUMAN'
named entity 'INDUCED'
named entity 'ENABLES'
named entity 'PATTERN'
named entity 'ROLE'
named entity 'PANDEMIC'
named entity 'NEEDED'
named entity 'PHOSPHOPROTEOMICS'
named entity 'PHOSPHOPROTEOME'
named entity 'ANTIVIRAL DRUG'
named entity 'INFLUENZA VIRUS'
named entity 'TREATMENT OPTIONS'
named entity 'BASED'
named entity 'KINASE'
named entity 'VIRUS INFECTION'
named entity 'SELECTED'
named entity 'SPECIFIC'
named entity 'CHANGES'
named entity 'INFLUENZA'
named entity 'POPULATION'
named entity 'CURRENT TREATMENT'
named entity 'AFFECT'
named entity 'OCCUR'
named entity 'NETWORK'
named entity 'NEW'
named entity 'LEADS'
named entity 'FOCUS'
named entity 'CULTURES'
named entity 'CELLULAR'
named entity 'NODE'
named entity 'ANNUAL'
named entity 'UNIQUE'
named entity 'HOST CELL'
named entity 'DECREASED'
named entity 'ITS'
named entity 'GRK2'
named entity 'SIGNALING'
named entity 'REPLICATION'
named entity 'OBSERVED'
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