Protein Plasticity and Peptide Editing in the MHC I Antigen Processing Pathway
Author(s) -
Tim Elliott,
Andy van Hateren
Publication year - 2018
Publication title -
biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.43
H-Index - 253
eISSN - 1520-4995
pISSN - 0006-2960
DOI - 10.1021/acs.biochem.7b01307
Subject(s) - antigen processing , major histocompatibility complex , peptide , antigen , microbiology and biotechnology , computational biology , chemistry , biology , computer science , biochemistry , mhc class i , genetics
Cytotoxic T lymphocytes (CTL) of the vertebrate immune system can eliminate pathogeninfected or malignantly transformed cells offering protection from infectious and noninfectious diseases. This protection is afforded by receptors expressed on the cell surface of CTLs, with each T cell receptor recognising a specific complex of an MHC I molecule bound to a particular peptide. In humans six MHC I allotypes can be expressed, each of which may bind a variety of peptides. Thus, thousands of different pMHC complexes are present on antigen presenting cells, where they are scanned by CTL, which may be activated if a cognate ligand is encountered.
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