<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Zonggen Peng</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0016554000</full_dataset_link><submitter_email>pumcpzg@126.com</submitter_email><submitter_affiliation>Chinese Academy of Medical Sciences &amp;amp; Peking Union Medical College</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>SARS-CoV-2 FSE RNA pull down combined with LC-MS/MS analysis</name><description>To identify potential cellular RNA-binding proteins (RBPs) that interact with the FSE RNA of SARS-CoV-2, biotinylated in vitro transcription (IVT) FSE RNA from the SARS-CoV-2 genome was incubated with lysates of H460 cells infected with human coronavirus OC43 (HCoV-OC43) and Huh7 cells infected with human coronavirus 229E (HCoV-229E). To exclude non-specific binders, a non-related RNA was used as a control.</description><dates><publication>Tue Apr 07 00:00:00 BST 2026</publication></dates><accession>PXD076663</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>