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Protein Structure and Folding
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- Protein Structure and FoldingOpen Access
Unconventional Peptide Presentation by Major Histocompatibility Complex (MHC) Class I Allele HLA-A*02:01: BREAKING CONFINEMENT
Journal of Biological ChemistryVol. 292Issue 13p5262–5270Published online: February 8, 2017- Soumya G. Remesh
- Massimo Andreatta
- Ge Ying
- Thomas Kaever
- Morten Nielsen
- Curtis McMurtrey
- and others
Cited in Scopus: 41Peptide antigen presentation by major histocompatibility complex (MHC) class I proteins initiates CD8+ T cell-mediated immunity against pathogens and cancers. MHC I molecules typically bind peptides with 9 amino acids in length with both ends tucked inside the major A and F binding pockets. It has been known for a while that longer peptides can also bind by either bulging out of the groove in the middle of the peptide or by binding in a zigzag fashion inside the groove. In a recent study, we identified an alternative binding conformation of naturally occurring peptides from Toxoplasma gondii bound by HLA-A*02:01.