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Figure 5


Fig. 5. Constructs used in this study. The ORF from hFBNRG3 was cloned in-frame with a myc epitope at the C-terminus of the protein (a) or an HA epitope in the N-terminal domain (b). Amino acids 3 to 55 were deleted in the myc-tagged construct (c). The ORF of hFBNRG3 was cloned in-frame after CFP (d). Extracellular and transmembrane (e) intracellular (f) or N-terminal domains (g) were deleted from the CFP-hFBNRG3 construct. A construct bearing the N-terminal domain and part of the EGF-like domain attached to CFP was also produced (h). Synaptotagmin I with a myc-epitope at the C-terminus (i) and a chimeric protein containing the 1-92 N-terminal aa of hFBNRG3 fused to synaptotagmin I myc (j) were also used.





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