Antigen degradation or presentation by MHC class I molecules via classical and non-classical pathways.

Abstract:

:Major histocompatibility complex (MHC) class I molecules usually present endogenous peptides at the cell surface. This is the result of a cascade of events involving various dedicated proteins like the peptide transporter associated with antigen processing (TAP) and the ER chaperone tapasin. However, alternative ways for class I peptide loading exist which may be highly relevant in a process called cross-priming. Both pathways are described here in detail. One major difference between these pathways is that the proteases involved in the generation of peptides are different. How proteases and peptidases influence peptide generation and degradation will be discussed. These processes determine the amount of peptides available for TAP translocation and class I binding and ultimately the immune response.

journal_name

Mol Immunol

journal_title

Molecular immunology

authors

Grommé M,Neefjes J

doi

10.1016/s0161-5890(02)00101-3

subject

Has Abstract

pub_date

2002-10-01 00:00:00

pages

181-202

issue

3-4

eissn

0161-5890

issn

1872-9142

pii

S0161589002001013

journal_volume

39

pub_type

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