Competition for Access to the Rat Major Histocompatibility Complex Class I Peptide-loading Complex Reveals Optimization of Peptide Cargo in the Absence of Transporter Associated with Antigen Processing (TAP) Association
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference45 articles.
1. Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules
2. Selective and ATP-Dependent Translocation of Peptides by the MHC-Encoded Transporter
3. Proteasome subunits encoded by the major histocompatibility complex are not essential for antigen presentation
4. Assembly and export of MHC class I peptide ligands
5. The N-terminal region of tapasin is required to stabilize the MHC class I loading complex
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1. Measuring Synthesis and Degradation of MHC Class I Molecules;Antigen Processing;2019
2. Plasticity of empty major histocompatibility complex class I molecules determines peptide-selector function;Molecular Immunology;2015-12
3. F pocket flexibility influences the tapasin dependence of two differentially disease-associated MHC Class I proteins;European Journal of Immunology;2015-02-14
4. Measuring Synthesis and Degradation of MHC Class I Molecules;Antigen Processing;2012-10-29
5. N-Linked Glycosylation Selectively Regulates the Generic Folding of HLA-Cw1;Journal of Biological Chemistry;2008-06
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