<HashMap><database>MassIVE</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://massive-ftp.ucsd.edu/v12/MSV000100665/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><submitter>Aykut Uren</submitter><full_dataset_link>https://massive.ucsd.edu/ProteoSAFe/dataset.jsp?task=21a00fd9ba4f4690b94c7e07f99b0f83</full_dataset_link><submitter_email>au26@georgetown.edu</submitter_email><sample_protocol></sample_protocol><repository>MassIVE</repository><file_size>10</file_size><ptm_modification>MS:1002864 - No post-translational-modifications are included in the identified peptides of this dataset</ptm_modification><data_protocol></data_protocol><omics_type>Proteomics</omics_type><instrument_platform>Orbitrap Fusion Lumos</instrument_platform><instrument_platform>nanoACQUITY UPLC</instrument_platform><species>Homo Sapiens (ncbitaxon:9606)</species><submitter_affiliation>Georgetown University Medical Center</submitter_affiliation><additional_accession>PXD073850</additional_accession></additional><is_claimable>false</is_claimable><name>ROME BioID2 raw proteomics data from ROME KO manuscript</name><description>For proteomics, samples were heated for 10 min at 95 degrees. After cooling down to room temperature, 4 uL of 500 mM IAA in 5%SDS was added to a final concentration of 40 mM and incubated in the dark for 30 min. Undissolved matter was centrifuged for 8 min at 13,000 x g. The supernatant was saved and used for downstream processing using a S-Trap column (ProtiFi, LLC).  Proteins were digested with sequencing-grade Lys-C/trypsin (Promega) by incubation at 37 degrees overnight.  Peptides were analyzed with a nanoAcquity UPLC system coupled with Orbitrap Fusion Lumos mass spectrometer (ThermoFisher) as previously described.</description><dates><publication>Fri Jan 30 10:01:00 GMT 2026</publication></dates><accession>MSV000100665</accession><cross_references/></HashMap>