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PXD017570-1

PXD017570 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleAn Approach to Spatiotemporally Resolve Protein Interaction Networks in Living Cells - B2AR_DOR
DescriptionSRM assays were generated for selected interactors of B2AR and DOR(MSV000084857), as well as for localization controls and ribosomal proteins (RPL18A, RPL28, RPL3, RPL35A, RPL6) as internal controls for normalization (Table S5 in publication). SRM assay generation was performed using Skyline. For all targeted proteins, proteotypic peptides and optimal transitions for identification and quantification were selected based on a spectral library generated from the shotgun MS experiments. The Skyline spectral library was used to extract optimal coordinates for the SRM assays, e.g., peptide fragments and peptide retention times. For each protein 1-4 peptides were selected based on intensity, peptide length as well as chromatographic performance. For each peptide the 4 best SRM transitions were selected based on intensity and peak shape. Digested peptide mixtures were analyzed by LC-SRM on a Thermo Scientific TSQ Quantiva MS system equipped with a Proxeon Easy nLC 1200 ultra high-pressure liquid chromatography and autosampler system. Samples were injected onto a C18 column (25 cm x 75 mm I.D. packed with ReproSil Pur C18 AQ 1.9 mm particles) in 0.1% formic acid and then separated with an 80 min gradient from 5% to 40% Buffer B (90% ACN/10% water/0.1% formic acid) at a flow rate of 300 nl/min. SRM acquisition was performed operating Q1 and Q3 at 0.7 unit mass resolution. For each peptide the best 4 transitions were monitored in a scheduled fashion with a retention time window of 4 min and a cycle time fixed to 2s. Argon was used as the collision gas at a nominal pressure of 1.5 mTorr. Collision energies were calculated by, CE = 0.0348 * (m/z) + 0.4551 and CE = 0.0271 * (m/z) + 1.5910 (CE, collision en- ergy and m/z, mass to charge ratio) for doubly and triply charged precursor ions, respectively. RF lens voltages were calculated by, RF= 0.1088 * (m/z) + 21.029 and RF= 0.1157 * (m/z) + 0.1157 (RF, RF lens voltage andm/z, mass to charge ratio) for doubly and triply charged precursor ions, respectively. SRM data were processed using Skyline. Protein significance analysis for the different time points was performed using MSstats. Normalization across samples was conducted based on selected global standard proteins (RPL18A, RPL28, RPL3, RPL35A, RPL6). Each protein was tested for abundance differences comparing DOR-APEX2 time points to the spatial references, PM-APEX2 and ENDO-APEX2. Proteins with an adjusted p-value < 0.05 were considered significant.
HostingRepositoryMassIVE
AnnounceDate2020-02-17
AnnouncementXMLSubmission_2020-02-17_18:57:35.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterMeena Choi
SpeciesList scientific name: Homo sapiens; common name: human; NCBI TaxID: 9606;
ModificationListNo PTMs are included in the dataset
InstrumentTSQ Quantiva
Dataset History
RevisionDatetimeStatusChangeLog Entry
02020-02-17 18:50:51ID requested
12020-02-17 18:57:36announced
Publication List
Lobingier BT, H, ΓΌ, ttenhain R, Eichel K, Miller KB, Ting AY, von Zastrow M, Krogan NJ, An Approach to Spatiotemporally Resolve Protein Interaction Networks in Living Cells. Cell, 169(2):350-360.e12(2017) [pubmed]
Keyword List
submitter keyword: GPCR, APEX, proximity biotinylation, protein-protein interactions
Contact List
Ruth Huttenhain
contact affiliationDepartment of Molecular and Cellular Pharmacology, UCSF
contact emailRuth.huttenhain@ucsf.edu
lab head
Meena Choi
contact affiliationNortheastern University
contact emailmnchoi67@gmail.com
dataset submitter
Full Dataset Link List
MassIVE dataset URI
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://massive.ucsd.edu/MSV000084966/