<?xml version="1.0" encoding="UTF-8" ?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-11T11:59:21Z</responseDate><request identifier="10.58160/DXXuylafJAhzRoUV" metadataPrefix="oai_dc" verb="GetRecord">https://www.radar-service.eu/oai/OAIHandler</request><GetRecord><record><header><identifier>10.58160/DXXuylafJAhzRoUV</identifier><datestamp>2026-04-24T07:51:56Z</datestamp></header><metadata><oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/"
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   <dc:identifier>https://dx.doi.org/10.58160/DXXuylafJAhzRoUV</dc:identifier>
   <dc:creator>Schöl, Marie</dc:creator>
   <dc:title>Proteomic data _ Identification of neutral sphingomyelinase-2 (NSM2) proximal proteins by APEX2-mediated proximity labeling in Jurkat cells</dc:title>
   <dc:publisher>University of Würzburg</dc:publisher>
   <dc:date>2024</dc:date>
   <dc:subject>Biology</dc:subject>
   <dc:subject>Other</dc:subject>
   <dc:subject>Immunology</dc:subject>
   <dc:subject>Other</dc:subject>
   <dc:subject>Sphingolipids </dc:subject>
   <dc:type>dataset</dc:type>
   <dc:subject>Dataset</dc:subject>
   <dc:source>Mass spectrometry based proteomics</dc:source>
   <dc:source>Trial</dc:source>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:rights>https://creativecommons.org/licenses/by/4.0/legalcode</dc:rights>
   <dc:contributor>Dölken, Lars</dc:contributor>
   <dc:description>Proteomic mass spectrometry data supplementing the data published in the thesis: Identification of NSM2 proximal proteins by APEX2-mediated proximity labeling in Jurkat cells. </dc:description>
   <dc:description>The csv files contain tables that list proteins identified by label free LC-MS and their Log2 Fold Changes (Log2FC) and p values. Information about the individual csv files can be found in the "readme.txt”.</dc:description>
   <dc:description>A proximity labeling strategy was used based on the engineered ascorbate peroxidase 2 (APEX2) to explore the neutral sphingomyelinase 2 (NSM2) proximitome, specifically in Jurkat cells. For this purpose, cell lines stably expressing NSM2 fused to APEX2 at the C-terminus were generated. NSM2-APEX2 proximal proteins covalently labeled with biotin were purified using streptavidin-coated beads and identified by mass spectrometry (MS). The first analysis of NSM2-APEX2 labeling by MS accurately identified proteins under steady-state conditions (published in 10.3390/ijms25063247).   Further, I applied the proximity labeling protocol to elucidate TNFα-induced alterations in the NSM2 proximitome within the first 5 minutes of stimulation (published in  10.3389/fimmu.2024.1435701).  The NSM2 proximal network and its TNFα-induced changes provide a valuable resource for further investigations into the involvement of NSM2 in the early signaling pathways triggered by TNFα.</dc:description>
   <dc:subject>Neutrale sphingomyelinase 2</dc:subject>
   <dc:subject>APEX2</dc:subject>
   <dc:subject>Sphingolipide</dc:subject>
   <dc:subject>Proximity labeling</dc:subject>
   <dc:subject>Protein network</dc:subject>
   <dc:contributor>Dölken, Lars</dc:contributor>
   <dc:language>eng</dc:language>
   <dc:relation>10.3389/fimmu.2024.1435701</dc:relation>
   <dc:relation>https://ror.org/018mejw64</dc:relation>
   <dc:format>application/x-tar</dc:format>
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