scholarly journals High-affinity reactions between antigen-specific T-cell receptors and peptides associated with allogeneic and syngeneic major histocompatibility complex class I proteins.

1994 ◽  
Vol 91 (24) ◽  
pp. 11487-11491 ◽  
Author(s):  
Y. Sykulev ◽  
A. Brunmark ◽  
T. J. Tsomides ◽  
S. Kageyama ◽  
M. Jackson ◽  
...  
2002 ◽  
Vol 76 (6) ◽  
pp. 2796-2803 ◽  
Author(s):  
Y. Y. Lawrence Yu ◽  
Michael R. Harris ◽  
Lonnie Lybarger ◽  
Lisa A. Kimpler ◽  
Nancy B. Myers ◽  
...  

ABSTRACT To persist in the presence of an active immune system, viruses encode proteins that decrease expression of major histocompatibility complex class I molecules by using a variety of mechanisms. For example, murine gamma-2 herpesvirus 68 expresses the K3 protein, which causes the rapid turnover of nascent class I molecules. In this report we show that certain mouse class I alleles are more susceptible than others to K3-mediated down regulation. Prior to their rapid degradation, class I molecules in K3-expressing cells exhibit impaired assembly with β2-microglobulin. Furthermore, K3 is detected predominantly in association with class I molecules lacking assembly with high-affinity peptides, including class I molecules associated with the peptide loading complex TAP/tapasin/calreticulin. The detection of K3 with class I assembly intermediates raises the possibility that molecular chaperones involved in class I assembly are involved in K3-mediated class I regulation.


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