PXD049182 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Proximity labeling of host factor ANXA3 in HCV infection reveals a novel LARP1 function in viral entry |
Description | Hepatitis C virus (HCV) infection is tightly connected to the lipid metabolism with lipid droplets (LDs) serving as assembly sites for progeny virions. A previous LD proteome analysis identified annexin A3 (ANXA3) as an important HCV host factor that is enriched at LDs in infected cells and required for HCV morphogenesis. To further characterize ANXA3 function in HCV, we performed proximity labeling using ANXA3-BioID2 as bait in HCV-infected cells. Two of the top proteins identified proximal to ANXA3 during HCV infection were the La-related protein 1 (LARP1) and the ADP ribosylation factor-like protein 8B (ARL8B), both of which have been previously described to act in HCV particle production. In follow-up experiments ARL8B functioned as a pro-viral HCV host factor without localizing to LDs und thus likely independent of ANXA3. In contrast, LARP1 interacts with HCV core protein in an RNA-dependent manner and is translocated to LDs by core. Knockdown of LARP1 decreased HCV spreading without altering HCV RNA replication or viral titers. Unexpectedly, entry of HCV particles and E1/E2-pseudotyped lentiviral particles was reduced by LARP1 depletion, whereas particle production was not altered. Using a recombinant vesicular stomatitis virus (VSV)ΔG entry assay, we showed that LARP1 depletion also decreased entry of VSV with VSV, MERS, and CHIKV glycoproteins. Therefore, our data expand the role of LARP1 as an HCV host factor that is most prominently involved in the early steps of infection, likely contributing to endocytosis of viral particles through the pleiotropic effect LARP1 has on the cellular translatome. |
HostingRepository | PRIDE |
AnnounceDate | 2024-04-17 |
AnnouncementXML | Submission_2024-04-17_04:54:44.091.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Bente Siebels |
SpeciesList | scientific name: Hepacivirus; NCBI TaxID: 11102; scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | iodoacetamide derivatized residue |
Instrument | Q Exactive |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2024-02-05 07:55:52 | ID requested | |
⏵ 1 | 2024-04-17 04:54:44 | announced | |
Publication List
Keyword List
submitter keyword: proteomics, virus entry, proximity labeling, host-pathogen interaction, lipid droplets,Hepatitis C virus (HCV) |
Contact List
Eva Herker |
contact affiliation | Institute of Virology, Philipps-University Marburg, Marburg, Germany |
contact email | eva.herker@uni-marburg.de |
lab head | |
Bente Siebels |
contact affiliation | Section for Mass spectrometry and Proteomics, University Medical Center Hamburg-Eppendorf |
contact email | b.siebels@uke.de |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD049182
- Label: PRIDE project
- Name: Proximity labeling of host factor ANXA3 in HCV infection reveals a novel LARP1 function in viral entry