PXD044405 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Identification of a direct interaction between the Fab domains of IgG antibodies and human FcRn upon IgG-FcRn complex formation |
Description | Chemical cross-linking coupled to mass spectrometry was used to study the interaction between IgG-type antibodies and the neonatal Fc receptor (FcRn). Different cross-linking chemistries were used, including disuccinimidyl suberate (DSS); a combination of pimelic dihydrazide (PDH) in combination with the zero-length cross-linking reagent, DMTMM; and the Xplex method using hexanediamine and N-hydroxybenzotriazole. |
HostingRepository | PRIDE |
AnnounceDate | 2024-12-03 |
AnnouncementXML | Submission_2024-12-03_01:41:24.261.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Alexander Leitner |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | iodoacetamide derivatized residue |
Instrument | LTQ Orbitrap Elite |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2023-08-07 01:21:12 | ID requested | |
⏵ 1 | 2024-12-03 01:41:24 | announced | |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: Chemical cross-linking |
DSS |
PDH |
DMTMM |
XPlex |
structural proteomics |
antibody – receptor interactions |
Contact List
Alexander Leitner |
contact affiliation | ETH Zurich, Institute of Molecular Systems Biology, Zurich, Switzerland |
contact email | leitner@imsb.biol.ethz.ch |
lab head | |
Alexander Leitner |
contact affiliation | ETH Zurich, Institute of Molecular Systems Biology |
contact email | leitner@imsb.biol.ethz.ch |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD044405
- Label: PRIDE project
- Name: Identification of a direct interaction between the Fab domains of IgG antibodies and human FcRn upon IgG-FcRn complex formation