<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Yongliang Zhang</submitter><species>Nicotiana Benthamiana</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0012273000</full_dataset_link><submitter_email>cauzhangyl@cau.edu.cn</submitter_email><submitter_affiliation>China Agricultural University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Proximity Profiling of Chloroplast–Endoplasmic Reticulum Membrane Contact Sites in Nicotiana benthamiana Using Split-TurboID During Viral Infection</name><description>We fused the N-terminus of TurboID to the chloroplast outer membrane protein OEP7 and the C-terminus to the endoplasmic reticulum membrane protein RTNLB2. When the chloroplast and endoplasmic reticulum come into close proximity to form membrane contact sites (MCSs), the split-TurboID is reconstituted into an active proximity-labeling enzyme that biotinylates nearby proteins. In this proteomic study, Barley stripe mosaic virus (BSMV) infection was used as the experimental variable.</description><dates><publication>Fri Jun 13 00:00:00 BST 2025</publication></dates><accession>PXD064967</accession><cross_references><TAXONOMY>4100</TAXONOMY></cross_references></HashMap>