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. Author manuscript; available in PMC: 2015 Apr 21.
Published in final edited form as: Prog Mol Biol Transl Sci. 2012;109:75–112. doi: 10.1016/B978-0-12-397863-9.00003-1

Fig. 3.

Fig. 3

I-proteasome-dependent pathways of protein degradation. I-proteasome-dependent proteolysis in an antigen-presenting cell (APC) generates peptides and polypeptides for MHC class I-restricted antigen presentation, and for functions other than antigen presentation. (A) The antigen-processing pathway for degradation of a cytosolic protein leading to loading of peptides into MHC class I and antigen presentation to the T cell receptor (TCR). (B) Degradation of a protein by i-proteasome resulting in the generation of a spliced peptide candidate for antigen presentation. (C) I-proteasome-mediated endoproteolytic activity generating large, potentially biologically active polypeptides from a precursor protein. Small peptides may also be produced and would be available for antigen presentation. (D) Some of the small peptides produced by i-proteasome activity may have biological activity. PM, plasma membrane; ER, endoplasmic reticulum.