Interaction of murine MHC class I molecules with tapasin and TAP enhances peptide loading and involves the heavy chain alpha3 domain

• Published in: The Journal of immunology (1950) Vol. 162; no. 3; pp. 1530 - 1540
• Main Authors: Suh, W K, Derby, M A, Cohen-Doyle, M F, Schoenhals, G J, Früh, K, Berzofsky, J A, Williams, D B
• Format: Journal Article
• Language: English
• Published: United States 01-02-1999
• Subjects: Amino Acid Sequence; Animals; Antigen Presentation; Antiporters - metabolism; ATP-Binding Cassette Sub-Family B Member 2; ATP-Binding Cassette Transporters - metabolism; Binding Sites - genetics; Biological Transport, Active; Cell Line; Cell Membrane - immunology; Endoplasmic Reticulum - immunology; Endoplasmic Reticulum - metabolism; H-2 Antigens - genetics; H-2 Antigens - metabolism; Histocompatibility Antigen H-2D; Humans; Immunoglobulins; Kinetics; Macromolecular Substances; Membrane Transport Proteins; Mice; Molecular Sequence Data; Point Mutation; T-Lymphocytes, Cytotoxic - immunology
• ISSN: 0022-1767

In human cells the association of MHC class I molecules with TAP is thought to be mediated by a third protein termed tapasin. We now show that tapasin is present in murine TAP-class I complexes as well. Furthermore, we demonstrate that a mutant H-2Dd molecule that does not interact with TAP due to a Glu to Lys mutation at residue 222 of the H chain (Dd(E222K)) also fails to bind to tapasin. This finding supports the view that tapasin bridges the association between class I and TAP and implicates residue 222 as a site of contact with tapasin. The inability of Dd(E222K) to interact with tapasin and TAP results in impaired peptide loading within the endoplasmic reticulum. However, significant acquisition of peptides can still be detected as assessed by the decay kinetics of cell surface Dd(E222K) molecules and by the finding that prolonged viral infection accumulates sufficient target structures to stimulate T cells at 50% the level observed with wild-type Dd. Thus, although interaction with tapasin and TAP enhances peptide loading, it is not essential. Finally, a cohort of Dd(E222K) molecules decays more rapidly on the cell surface compared with wild-type Dd molecules but much more slowly than peptide-deficient molecules. This suggests that some of the peptides obtained in the absence of an interaction with tapasin and TAP are suboptimal, suggesting a peptide-editing function for tapasin/TAP in addition to their role in enhancing peptide loading.