The inhibition of early N-glycan processing targets TRP-2 to degradation in B16 melanoma cells

J Biol Chem. 2003 Jul 18;278(29):27035-42. doi: 10.1074/jbc.M303167200. Epub 2003 Apr 28.


Tyrosinase-related protein-2 (TRP-2) is a DOPAchrome tautomerase catalyzing a distal step in the melanin synthesis pathway. Similar to the other two melanogenic enzymes belonging to the TRP gene family, tyrosinase and TRP-1, TRP-2 is expressed in melanocytes and melanoma cells. Despite the increasing evidence of its efficiency as a melanoma antigen, little is known about the maturation and intracellular trafficking of TRP-2. Here we show that TRP-2 is mainly distributed in the TGN of melanoma cells instead of being confined solely to melanosomes. This, together with the plasma membrane occasional localization observed by immunofluorescence, suggest the TRP-2 participation in a recycling pathway, which could include or not the melanosomes. Using pulse-chase experiments we show that the TRP-2 polypeptide folds in the endoplasmic reticulum (ER) in the presence of calnexin, until it reaches a dithiothreitol-resistant conformation enabling its ER exit to the Golgi. If N-glycosylation inhibitors prevent the association with calnexin, the TRP-2 nascent chain undergoes an accelerated degradation process. This process is delayed in the presence of proteasomal inhibitors, indicating that the misfolded chain is retro-translocated from the ER into the cytosol and degraded in proteasomes. This is a rare example in which calnexin although indispensable for the nascent chain folding is not required for its targeting to degradation. Therefore TRP-2 may prove to be a good model to document the calnexin-independent retro-translocation process of proteasomally degraded proteins. Clearly, TRP-2 has a distinct maturation pathway from tyrosinase and TRP-1 and possibly a second regulatory function within the cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport, Active
  • Calnexin / metabolism
  • Calreticulin / metabolism
  • Cysteine Endopeptidases / metabolism
  • Endoplasmic Reticulum / metabolism
  • Golgi Apparatus / metabolism
  • Intramolecular Oxidoreductases / chemistry
  • Intramolecular Oxidoreductases / metabolism*
  • Melanoma, Experimental / metabolism*
  • Melanosomes / metabolism
  • Mice
  • Multienzyme Complexes / metabolism
  • Polysaccharides / metabolism*
  • Proteasome Endopeptidase Complex
  • Protein Conformation
  • Protein Folding
  • Protein Processing, Post-Translational
  • Subcellular Fractions / metabolism
  • Tumor Cells, Cultured
  • trans-Golgi Network / metabolism


  • Calreticulin
  • Multienzyme Complexes
  • Polysaccharides
  • Calnexin
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex
  • Intramolecular Oxidoreductases
  • dopachrome isomerase