Translating DRiPs: progress in understanding viral and cellular sources of MHC class I peptide ligands
- PMID: 21416150
- PMCID: PMC3393103
- DOI: 10.1007/s00018-011-0656-z
Translating DRiPs: progress in understanding viral and cellular sources of MHC class I peptide ligands
Abstract
It has been 15 years since we proposed the defective ribosomal product (DRiP) hypothesis to explain the rapid presentation of viral peptides by MHC class I molecules on the surface of infected cells. Here, we review the evidence for the contribution of DRiPs to antigen processing, pointing to the uncertainties regarding the physical nature of DRiPs, and emphasizing recent findings suggesting that peptide generation is a specialized process involving compartmentalized translation.
References
-
- Oxenius A, Bachmann MF, Ashton-Rickardt PG, et al. Presentation of endogenous viral proteins in association with major histocompatibility complex class II: on the role of intracellular compartmentalization, invariant chain and the TAP transporter system. Eur J Immunol. 1995;25(12):3402–3411. doi: 10.1002/eji.1830251230. - DOI - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials