PXD011690 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | A study into the ADP-ribosylome of IFN--stimulated THP-1 human macrophage-like cells identifies ARTD8/PARP14 and ARTD9/PARP9 ADP-ribosylation |
Description | ADP-ribosylation is a post-translational modification that, until recently, has remained elusive to study at the cellular level. Previously dependent on radioactive tracers to identify ADP-ribosylation targets, several advances in mass spectrometric workflows now permit global identification of ADP-ribosylated substrates. In this study, we capitalized on two ADP-ribosylation enrichment strategies, and multiple activation methods performed on the Orbitrap Fusion Lumos, to identify IFN--induced ADP-ribosylation substrates in macrophages. The ADP-ribosyl binding protein, Af1521, was used to enrich ADP-ribosylated peptides, and the anti-poly-ADP-ribosyl antibody, 10H, was used to enrich ADP-ribosylated proteins. ADP-ribosyl-specific mass spectra were further enriched by an ADP-ribose product ion triggered EThcD and HCD activation strategy, in combination with multiple acquisitions that segmented the survey scan into smaller ranges. HCD and EThcD resulted in overlapping and unique ADP-ribosyl peptide identifications, with HCD providing more peptide identifications but EThcD providing more reliable ADP-ribosyl acceptor sites. Our acquisition strategies also resulted in the first ever characterization of ADP-ribosyl on three poly-ADP-ribose polymerases, ARTD9/PARP9, ARTD10/PARP10, and ARTD8/PARP14. IFN- increased the ADP-ribosylation status of ARTD9/PARP9, ARTD8/PARP14, and proteins involved in RNA processes. This study therefore summarizes specific molecular pathways at the intersection of IFN- and ADP-ribosylation signaling pathways. |
HostingRepository | PRIDE |
AnnounceDate | 2020-01-27 |
AnnouncementXML | Submission_2020-01-27_03:57:49.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Sasha Singh |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | adenosine diphosphoribosyl (ADP-ribosyl) modified residue |
Instrument | Orbitrap Fusion Lumos |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2018-11-13 08:16:16 | ID requested | |
1 | 2019-08-22 07:12:02 | announced | |
2 | 2019-08-26 23:43:45 | announced | Updated publication reference for PubMed record(s): 30848916. |
⏵ 3 | 2020-01-27 03:57:51 | announced | 2020-01-27: Updated publication reference for PubMed record(s): 30848916. |
Publication List
Higashi H, Maejima T, Lee LH, Yamazaki Y, Hottiger MO, Singh SA, Aikawa M, -Stimulated THP-1 Human Macrophage-like Cells Identifies ARTD8/PARP14 and ARTD9/PARP9 ADP-Ribosylation. J Proteome Res, 18(4):1607-1622(2019) [pubmed] |
Keyword List
submitter keyword: higher-energy collision dissociation (HCD), electron transfer higher-energy collision dissociation (EThcD), Orbitrap Fusion Lumos, gas phase segmentation, parallel reaction monitoring (PRM), proteomics, post-translational modification (PTM) |
Contact List
SASHA SINGH |
contact affiliation | BRIGHAM AND WOMEN'S HOSPITAL, HARVARD MEDICAL SCHOOL |
contact email | SASINGH@BWH.HARVARD.EDU |
lab head | |
Sasha Singh |
contact affiliation | Brigham and Women's Hospital, Harvard Medical School |
contact email | sasingh@partners.org |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
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[ - ]
- PRIDE
- PXD011690
- Label: PRIDE project
- Name: A study into the ADP-ribosylome of IFN--stimulated THP-1 human macrophage-like cells identifies ARTD8/PARP14 and ARTD9/PARP9 ADP-ribosylation