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