PXD000244 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | 14-3-3 membrane protein interactome |
Description | To elucidate more details of the interaction between the PM (plasma membrane) H+ ATPase and 14-3-3 and to identify novel interaction partners of this multi-protein complex we developed a strategy for identification of protein-protein interactions using /in vivo/ formaldehyde cross-linking in combination with immunoprecipitation and MS-based protein identification. This method identified numerous proteins which may interact with the PM H+ ATPase to regulate its activity or to transmit environmental signals across the plasma membrane. All tryptic peptides mixtures were analyzed by LC-MS/MS using a nanoflow Easy-nLC System (Thermo Scientific, http://www.thermo.com) and an LTQ-Orbitrap hybrid mass spectrometer(Thermo Scientific) as a mass analyser. Peptides were separated on a 75 µm C18 analytical column (Integrafrit Biobasic, New Objectives, USA) with a linear gradient (10 to 64% acetonitrile) and sprayed directly into the LTQ-Orbitrap mass spectrometer. Data processing: Fragmentation spectra were searched against the NCBI non-redundant protein database (www.ncbi.nlm.nih.gov) with taxonomic restriction to all plant species using the Mascot software (version 2.2, Matrix Science, UK; www.matrixscience.com ) with the following search parameters: trypsin as cleavage enzyme, peptide mass tolerance 300 ppm, MS/MS tolerance 0.8 Da, cysteine carbamidomethylation as fixed modification, methionine oxidation as variable modification. Only peptides longer than 5 amino acids were considered. Peptides were accepted automatically if they displayed a Mascot score higher than 47 which was the Mascot significance score threshold (p < 0.01). False positive rate as estimated from a search against the decoy NCBI database was 1.34%. |
HostingRepository | PRIDE |
AnnounceDate | 2024-10-22 |
AnnouncementXML | Submission_2024-10-22_04:29:25.056.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Waltraud Schulze |
SpeciesList | scientific name: Lilium; NCBI TaxID: 4688; |
ModificationList | monohydroxylated residue; iodoacetamide derivatized residue |
Instrument | LTQ Orbitrap |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2013-05-07 13:35:13 | ID requested | |
1 | 2016-05-10 00:16:51 | announced | |
⏵ 2 | 2024-10-22 04:29:29 | announced | 2024-10-22: Updated project metadata. |
Publication List
10.1016/j.jprot.2014.05.001; |
Pertl-Obermeyer H, Schulze WX, Obermeyer G, In vivo cross-linking combined with mass spectrometry analysis reveals receptor-like kinases and Ca(2+) signalling proteins as putative interaction partners of pollen plasma membrane H(+) ATPases. J Proteomics, 108():17-29(2014) [pubmed] |
Keyword List
curator keyword: Biological |
submitter keyword: plasma membrane proton ATPase, cross linking, interaction partners, 14-3-3 protein, LC-MS/MS |
Contact List
Waltraud Schulze |
contact affiliation | Universität Hohenheim, Department of Plant Systems Biology |
contact email | wschulze@uni-hohenheim.de |
lab head | |
Waltraud Schulze |
contact affiliation | Metabolic Networks |
contact email | wschulze@mpimp-golm.mpg.de |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD000244
- Label: PRIDE project
- Name: 14-3-3 membrane protein interactome