<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Zhiyuan Chen</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0016392000</full_dataset_link><submitter_email>drchenzy@whu.edu.cn</submitter_email><submitter_affiliation>Renmin Hospital of Wuhan University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Immunoprecipitation-mass spectrometry (IP-MS) of USP15-interacting proteins in 786-O cells</name><description>786-O cells were lysed in IP buffer and processed for immunoprecipitation with anti-USP15 or normal rabbit IgG for 6 h at 4 °C. The immune complexes were incubated with Pierce Protein A/G Magnetic Beads (Thermo Scientific) overnight at 4 °C and washed with IP buffer. After SDS-PAGE and Coomassie brilliant blue staining, the gel was cut into sections and digested with trypsin. For each sample, 2 µg of total peptides were separated and analyzed with a nano-UPLC (nanoElute2) coupled to a timsTOF Pro2 mass spectrometer (Bruker) with a nano-electrospray ion source. Then the raw MS files were processed using PaSER software (Version 2023) and the built-in DDA-ProluCID-GPU search engine.</description><dates><publication>Thu Mar 26 00:00:00 GMT 2026</publication></dates><accession>PXD076226</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>