<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Steinmetz TD</submitter><funding>Universit?t zu K?ln</funding><funding>Deutsche Forschungsgemeinschaft</funding><pagination>1615-1633</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11077586</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(5)</volume><pubmed_abstract>Autophagy supervises the proteostasis and survival of B lymphocytic cells. &lt;i>Trk-fused gene&lt;/i> (TFG) promotes autophagosome-lysosome flux in murine CH12 B cells, as well as their survival. Hence, quantitative proteomics of CH12&lt;i>tfg&lt;/i>KO and WT B cells in combination with lysosomal inhibition should identify proteins that are prone to lysosomal degradation and contribute to autophagy and B cell survival. Lysosome inhibition via NH&lt;sub>4&lt;/sub>Cl unexpectedly reduced a number of proteins but increased a large cluster of translational, ribosomal, and mitochondrial proteins, independent of TFG. Hence, we propose a role for lysosomes in ribophagy in B cells. TFG-regulated proteins include CD74, BCL10, or the immunoglobulin JCHAIN. Gene ontology (GO) analysis reveals that proteins regulated </pubmed_abstract><journal>Journal of proteome research</journal><pubmed_title>Identification of TFG- and Autophagy-Regulated Proteins and Glycerophospholipids in B Cells.</pubmed_title><pmcid>PMC11077586</pmcid><funding_grant_id>EXC-2189  390939984</funding_grant_id><funding_grant_id>GK1660</funding_grant_id><funding_grant_id>939/6-1</funding_grant_id><funding_grant_id>TRR130</funding_grant_id><funding_grant_id>403222702 - SFB 1381</funding_grant_id><pubmed_authors>Castiglione K</pubmed_authors><pubmed_authors>Jack HM</pubmed_authors><pubmed_authors>Himmelreich AK</pubmed_authors><pubmed_authors>Brodesser S</pubmed_authors><pubmed_authors>Mielenz D</pubmed_authors><pubmed_authors>Steinmetz TD</pubmed_authors><pubmed_authors>Schulz SR</pubmed_authors><pubmed_authors>Thomas J</pubmed_authors><pubmed_authors>Warscheid B</pubmed_authors><pubmed_authors>Reimann L</pubmed_authors><pubmed_authors>Golombek F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of TFG- and Autophagy-Regulated Proteins and Glycerophospholipids in B Cells.</name><description>Autophagy supervises the proteostasis and survival of B lymphocytic cells. &lt;i>Trk-fused gene&lt;/i> (TFG) promotes autophagosome-lysosome flux in murine CH12 B cells, as well as their survival. Hence, quantitative proteomics of CH12&lt;i>tfg&lt;/i>KO and WT B cells in combination with lysosomal inhibition should identify proteins that are prone to lysosomal degradation and contribute to autophagy and B cell survival. Lysosome inhibition via NH&lt;sub>4&lt;/sub>Cl unexpectedly reduced a number of proteins but increased a large cluster of translational, ribosomal, and mitochondrial proteins, independent of TFG. Hence, we propose a role for lysosomes in ribophagy in B cells. TFG-regulated proteins include CD74, BCL10, or the immunoglobulin JCHAIN. Gene ontology (GO) analysis reveals that proteins regulated </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-06-02T06:54:37.736Z</modification><creation>2026-04-15T03:15:35.033Z</creation></dates><accession>S-EPMC11077586</accession><cross_references><pubmed>38649144</pubmed><doi>10.1021/acs.jproteome.3c00713</doi></cross_references></HashMap>