dc.contributor.author
Gadalla, Mohamed Rasheed
dc.contributor.author
Morrison, Eliot
dc.contributor.author
Serebryakova, Marina V.
dc.contributor.author
Han, Xueijiao
dc.contributor.author
Wolff, Thorsten
dc.contributor.author
Freund, Christian
dc.contributor.author
Kordyukova, Larisa
dc.contributor.author
Veit, Michael
dc.date.accessioned
2021-05-12T07:47:08Z
dc.date.available
2021-05-12T07:47:08Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/30572
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-30312
dc.description.abstract
Influenza A viruses contain two S-acylated proteins, the ion channel M2 and the glycoprotein hemagglutinin (HA). Acylation of the latter is essential for virus replication. Here we analysed the expression of each of the 23 members of the family of ZDHHC acyltransferases in human airway cells, the site of virus replication. RT-PCR revealed that every ZDHHC acyltransferase (except ZDHHC19) is expressed in A549 and Calu cells. Interestingly, expression of one ZDHHC, ZDHHC22, is upregulated in virus-infected cells; this effect is more pronounced after infection with an avian compared to a human virus strain. The viral protein NS1 triggers ZDHHC22 expression in transfected cells, whereas recombinant viruses lacking a functional NS1 gene did not cause ZDHHC22 upregulation. CRISPR/Cas9 technology was then used to knock-out the ZDHHC22 gene in A549 cells. However, acylation of M2 and HA was not reduced, as analysed for intracellular HA and M2 and the stoichiometry of S-acylation of HA incorporated into virus particles did not change according to MALDI-TOF mass spectrometry analysis. Comparative mass spectrometry of palmitoylated proteins in wt and Delta ZDHHC22 cells identified 25 potential substrates of ZDHHC22 which might be involved in virus replication.
en
dc.format.extent
17 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
Hemagglutinin
en
dc.subject
mass spectrometry
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::570 Biowissenschaften; Biologie
dc.title
NS1‐mediated upregulation of ZDHHC22 acyltransferase in influenza a virus infected cells
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
e13322
dcterms.bibliographicCitation.doi
10.1111/cmi.13322
dcterms.bibliographicCitation.journaltitle
Cellular Microbiology
dcterms.bibliographicCitation.number
6
dcterms.bibliographicCitation.volume
23
dcterms.bibliographicCitation.url
https://doi.org/10.1111/cmi.13322
refubium.affiliation
Veterinärmedizin
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Virologie
refubium.affiliation.other
Institut für Chemie und Biochemie
refubium.funding
DEAL Wiley
refubium.note.author
Die Publikation wurde aus Open Access Publikationsgeldern der Freien Universität Berlin gefördert.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1462-5822
refubium.resourceType.provider
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