spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


Right arrow Help viewing high resolution images
Right arrow Return to article
(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)



Fig. 7. Di-leucine-based motifs are important for the intracellular localization and trafficking of syntaxins 7 and 8. A putative di-leucine-based motif is present in the cytoplasmic domains of syntaxin 7 (amino acids 162-168) and syntaxin 8 (amino acids 77-83). Mutations in these motifs were made as indicated by underlining. Clone 9 cells were transfected with syn7-mut (a,b) or syn8-mut (d,e), each of which was fused to an N-terminal HA tag. For intracellular localization analysis, the cells were incubated for 12 hours (a,d) or 24 hours (b,e) and stained with anti-HA antibody. For antibody uptake experiments, Clone 9 cells were transfected with mutants in which the C-termini were fused to three c-myc tags (c,f). After 24 hours incubation, the cells were incubated for 3 hours in the presence of mouse anti-c-myc antibody before fixing. The cells were fixed and stained with FITC-conjugated anti-mouse IgG. (a-c) Syn7-mut was localized to endosomes and at the plasma membrane. In antibody uptake experiments, labeling was found only at the plasma membrane. (d-f) Syn8-mut was localized to the perinuclear Golgi region. No staining was observed in antibody uptake experiments.





Right arrow Return to article