Irreversible inactivation of ISG15 by a viral leader protease enables alternative infection detection strategies

In response to viral infection, cells mount a potent inflammatory response that relies on ISG15 and ubiquitin posttranslational modifications. Many viruses use deubiquitinases and deISGylases that reverse these modifications and antagonize host signaling processes. We here reveal that the leader pro...

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Vydané v:Proceedings of the National Academy of Sciences - PNAS Ročník 115; číslo 10; s. 2371
Hlavní autori: Swatek, Kirby N, Aumayr, Martina, Pruneda, Jonathan N, Visser, Linda J, Berryman, Stephen, Kueck, Anja F, Geurink, Paul P, Ovaa, Huib, van Kuppeveld, Frank J M, Tuthill, Tobias J, Skern, Tim, Komander, David
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 06.03.2018
Predmet:
Crystallography
Cytokines - chemistry
Cytokines - metabolism
Endopeptidases - chemistry
Endopeptidases - metabolism
HeLa Cells
Host-Pathogen Interactions
Humans
Models, Molecular
Protein Binding
Substrate Specificity
Ubiquitin - metabolism
Ubiquitins - chemistry
Ubiquitins - metabolism
FMDV
viral signaling
ISG15
structure
ubiquitin
ISSN:1091-6490, 1091-6490
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Shrnutí:In response to viral infection, cells mount a potent inflammatory response that relies on ISG15 and ubiquitin posttranslational modifications. Many viruses use deubiquitinases and deISGylases that reverse these modifications and antagonize host signaling processes. We here reveal that the leader protease, Lb , from foot-and-mouth disease virus (FMDV) targets ISG15 and to a lesser extent, ubiquitin in an unprecedented manner. Unlike canonical deISGylases that hydrolyze the isopeptide linkage after the C-terminal GlyGly motif, Lb cleaves the peptide bond preceding the GlyGly motif. Consequently, the GlyGly dipeptide remains attached to the substrate Lys, and cleaved ISG15 is rendered incompetent for reconjugation. A crystal structure of Lb bound to an engineered ISG15 suicide probe revealed the molecular basis for ISG15 proteolysis. Importantly, anti-GlyGly antibodies, developed for ubiquitin proteomics, are able to detect Lb cleavage products during viral infection. This opens avenues for infection detection of FMDV based on an immutable, host-derived epitope.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:1091-6490
1091-6490
DOI:10.1073/pnas.1710617115