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Precise score for the prediction of peptides cleaved by the proteasome
Author(s) -
Ido Ginodi,
Tal ViderShalit,
Lea Tsaban,
Yoram Louzoun
Publication year - 2008
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btm616
Subject(s) - epitope , cleavage (geology) , proteasome , peptide , cytotoxic t cell , mhc class i , context (archaeology) , computational biology , chemistry , biology , in vitro , microbiology and biotechnology , biochemistry , antigen , immunology , paleontology , fracture (geology)
An 8-10mer can become a cytotoxic T lymphocyte epitope only if it is cleaved by the proteasome, transported by TAP and presented by MHC-I molecules. Thus most of the epitopes presented to cytotoxic T cells in the context of MHC-I molecules are products of intracellular proteasomal cleavage. These products are not random, as peptide production is a function of the precise sequence of the proteins processed by the proteasome.

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