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Untitled - D Ank Unlimited

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antigen presentation 53 antigen presentation<br />

C<br />

Presentation of MHC histocompatibility antigen HLA-B270S complexes<br />

with nonapeptide ARG-ARG-ILE-LYS-ALA-ILE-THR-LEU-LYS. The<br />

C terminal amino acid of the antigen-binding domain is protected by an<br />

N-methyl group. Three water molecules bridge the binding of the peptide<br />

to the histocompatibility protein.<br />

endoplasmic reticulum. Following cleavage of the invariant<br />

chain, DM molecules remove a tiny piece of invariant<br />

chain from the MHC molecules’ peptide-binding grooves.<br />

Following complexing of extracellular-derived peptide with<br />

Class I<br />

TGN<br />

Golgi<br />

Endoplasmic<br />

reticulum<br />

N<br />

C<br />

N<br />

αβli<br />

the class II MHC molecule, the MHC–peptide complex<br />

is transported to the cell surface where presentation to<br />

CD4 + cells occurs. Proteins in the cytosol, such as those<br />

derived from viruses, may be processed through the class<br />

I MHC route of antigen presentation. The multiprotein<br />

complex in the cytoplasm, known as the proteasome, leads<br />

to proteolytic degradation of proteins in the cytoplasm<br />

to yield many of the peptides that are presented by class<br />

I MHC molecules. TAP molecules transport peptides<br />

from the cytoplasm to the endoplasmic reticulum where<br />

they interact and bind to class I MHC dimeric molecules.<br />

Once the class I MHC molecules have become stabilized<br />

through peptide binding, the complex leaves the endoplasmic<br />

reticulum, entering the Golgi apparatus en route to the<br />

surface of the cell. Thus, mechanisms are provided through<br />

MHC-restricted antigen presentation to guarantee that<br />

peptides derived from extracellular microbial proteins can<br />

be presented by class II MHC molecules to CD4 + helper T<br />

cells and that peptides derived from intracellular microbes<br />

can be presented by class I MHC molecules to CD8 + cytotoxic<br />

T lymphocytes. The generation of microbial peptides<br />

produced through antigen processing to combine with self<br />

Class II<br />

LFA-3<br />

Early<br />

endosome<br />

Processing pathways for class II-restricted antigen presentation.<br />

MHC<br />

Class II<br />

APC<br />

(macrophage or dendritic cell)<br />

αβ<br />

ICAM-1<br />

Ag<br />

peptide<br />

Late<br />

endosome<br />

Lysosome<br />

LFA-1<br />

Antigen presentation.<br />

TCR<br />

CD4 CD2<br />

T cell<br />

A

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