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Selective export of MHC class I molecules from the ER after their dissociation from TAP.

Authors
  • Et, Spiliotis
  • H, Manley
  • M, Osorio
  • Mc, Zúñiga
  • M, Edidin
Type
Published Article
Journal
Immunity
Publisher
Elsevier
Volume
13
Issue
6
Pages
841–851
Source
UCSC Cancer biomedical-ucsc
License
Unknown

Abstract

It has been assumed that upon dissociation from TAP, MHC class I molecules exit the ER by nonselective bulk flow. We now show that exit must occur by association with cargo receptors. Inconsistent with exit by bulk flow, loading of MHC class I molecules with high-affinity peptides triggers dissociation from TAP but has no effect on rates of ER-to-Golgi transport. Moreover, peptide-loaded MHC class I molecules accumulate at ER exit sites from which TAP molecules are excluded. Consistent with receptor-mediated exit, ER-to-Golgi transport of MHC class I molecules is independent of their cytoplasmic tails, which themselves lack ER export motifs. In addition, we show that MHC class I molecules associate with the putative cargo receptor BAP31.

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