<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Rui Wang</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0007707000</full_dataset_link><submitter_email>wangrui@szbl.ac.cn</submitter_email><submitter_affiliation>Shenzhen Bay Laboratory</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Target identification of dioxygenated amide derivatives interacting proteins</name><description>To identify the direct binding proteins of dioxygenated amide by chemical proteomics, we firstly evaluated the efficiency of optimized probe 6D-PP probe labelling the E. coli bacterial proteomes by in-gel fluorescence. Briefly, the E. coli bacterial lysates were incubated with 100 M probe 6D-PP under 37 °C for 2 h and exposed to 365 nm UV light for 0.5 h to initiate photo-crosslinking. A blank control with only DMSO, a negative control without UV light and a control sample with pretreatment of 500 M D-PP6-C were also included. After conjugation with the TAMRA-N3 by copper-catalyzed azide-alkyne cycloaddition (CuAAC) click chemistry for another 1 h, the probe 6D-PP labelled proteins were separated with 12% SDS-PAGE and imaged by in-gel fluorescence (Fig.3B).  The probe 6D-PP probe showed an efficiently UV-dependent and probe 6D-PP specific labelling, supporting it’s readily applicable in ABPP (activity-based protein profiling) experiment.</description><dates><publication>Fri Dec 08 00:00:00 GMT 2023</publication></dates><accession>PXD047691</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>