<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Robin W. Klemm</submitter><journal>The Journal of Cell Biology</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-JCBD-200901145</full_dataset_link><attach_to>JCB</attach_to><legend>sec6-4 cells expressing the immunoisolation bait Gap1GFPLTLM9 and the soluble secreted marker InvRFP from the inducible promoter Gals. Gap1GFPLTLM9 localizes to dot-like structures which is typical for the Golgi apparatus and endosomes in yeast. InvRFP is accumulating intracellularly at the restrictive temperature 37˚C. It is not secreted (shown also biochemically in Fig S3B).</legend><legend>sec6-4 cells expressing the immunoisolation bait FusMidGFPLTLM9 and the soluble secreted marker InvRFP from the inducible promoter Gals. FusMidGFPLTLM9 localizes to the plasma membrane at permissive temperature 24˚C.  InvRFP is not accumulating intracellularly at the permissive temperature 24˚C. Instead it is secreted (also shown biochemically in Fig S3B).</legend><legend>sec6-4 cells expressing the immunoisolation bait FusMidGFPLTLM9 and the soluble secreted marker InvRFP from the inducible promoter Gals. The immunoisolation bait FusMidGFPLTLM9 is accumulating intracellularly at the restrictive temperature 37˚C. &lt;br />InvRFP is accumulating intracellularly at the restrictive temperature 37˚C. It is not secreted (shown also biochemically in Fig S3B).</legend><legend>sec6-4 cells expressing the immunoisolation bait Gap1GFPLTLM9 and the soluble secreted marker InvRFP from the inducible promoter Gals. Gap1GFPLTLM9 localizes to dot-like structures which is typical for the Golgi apparatus and endosomes in yeast. InvRFP is not accumulating intracellularly at the permissive temperature 24˚C. Instead, it is secreted (shown also biochemically in Fig. S3B).</legend><repository>bioimages</repository><figure_sub>Image 1583 (Figure 1 - B)</figure_sub><figure_sub>Image 1582 (Figure 1 - B)</figure_sub><figure_sub>Image 1581 (Figure 1 - A)</figure_sub><figure_sub>Figure 1 - A</figure_sub><figure_sub>Image 1580 (Figure 1 - A)</figure_sub><figure_sub>Figure 1</figure_sub><figure_sub>Figure 1 - B</figure_sub><pubmed_authors>Mathias J. Gerl</pubmed_authors><pubmed_authors>Charles Ferguson</pubmed_authors><pubmed_authors>Andrej Shevchenko</pubmed_authors><pubmed_authors>Christer S. Ejsing</pubmed_authors><pubmed_authors>Tomasz J. Proszynski</pubmed_authors><pubmed_authors>Quentin de Robillard</pubmed_authors><pubmed_authors>Michal A. Surma</pubmed_authors><pubmed_authors>Kai Simons</pubmed_authors><pubmed_authors>Robin W. Klemm</pubmed_authors><pubmed_authors>Julio L. Sampaio</pubmed_authors><pubmed_authors>Hermann-Josef Kaiser</pubmed_authors></additional><is_claimable>false</is_claimable><name>Segregation of sphingolipids and sterols during formation of secretory vesicles at the trans-Golgi network</name><description/><dates><release>2009-05-11T11:17:29Z</release><modification>2018-11-29T11:17:29Z</modification><creation>2018-11-29T11:17:29Z</creation></dates><accession>S-JCBD-200901145</accession><cross_references><doi>10.1083/jcb.200901145</doi></cross_references></HashMap>