Defective ribosomal products are the major source of antigenic peptides endogenously generated from influenza A virus neuraminidase.

TitleDefective ribosomal products are the major source of antigenic peptides endogenously generated from influenza A virus neuraminidase.
Publication TypeJournal Article
Year of Publication2010
AuthorsDolan BP, Li L, Takeda K, Bennink JR, Yewdell JW
JournalJournal of immunology (Baltimore, Md. : 1950)
Volume184
Issue3
Pagination1419-24
Date Published2010 Feb 1
ISSN1550-6606
KeywordsAmino Acid Sequence, Animals, Antigen Presentation, Antigens, Viral, Cell Line, Dendritic Cells, Dogs, Enzyme Activation, Enzyme Stability, Epitopes, Fibroblasts, H-2 Antigens, Influenza A Virus, H1N1 Subtype, L Cells (Cell Line), Mice, Molecular Sequence Data, Monocytes, Neuraminidase, Orthomyxoviridae Infections, Ovalbumin, Peptide Fragments, Protein Biosynthesis, Protein Folding, Protein Transport, Ribosomal Proteins
Abstract

The defective ribosomal product (DRiP) hypothesis of endogenous Ag processing posits that rapidly degraded forms of nascent proteins are a major source of peptide ligands for MHC class I molecules. Although there is broad experimental support for the DRiP hypothesis, careful kinetic analysis of the generation of defined peptide class I complexes has been limited to studies of recombinant vaccinia viruses expressing genes derived from other organisms. In this study, we show that insertion of the SIINFEKL peptide into the stalk of influenza A virus neuraminidase (NA) does not detectably modify NA folding, degradation, transport, or sp. act. when expressed in its natural context of influenza A virus infection. Using the 25-D1.16 mAb specific for K(b)-SIINFEKL to precisely quantitate cell surface complexes by flow cytometry, we demonstrate that SIINFEKL is generated in complete lockstep with initiation and abrogation of NA biosynthesis in both L-K(b) fibroblast cells and DC2.4 dendritic/monocyte cells. SIINFEKL presentation requires active proteasomes and TAP, consistent with its generation from a cytosolic DRiP pool. From the difference in the shutoff kinetics of K(b)-SIINFEKL complex expression following protein synthesis versus proteasome inhibition, we estimate that the t(1/2) of the biosynthetic source of NA peptide is approximately 5 min. These observations extend the relevance of the DRiP hypothesis to viral proteins generated in their natural context.

DOI10.4049/jimmunol.0901907
Alternate JournalJ. Immunol.