The final touches make perfect the peptide-MHC class I repertoire

被引:80
作者
Hammer, Gianna Elena [1 ]
Kanaseki, Takayuki [1 ]
Shastri, Nilabh [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Div Immunol, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.immuni.2007.04.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Major histocompatibility complex (MHC) class I molecules present short, perfectly cleaved peptides on the cell surface for immune surveillance by CD8(+) T cells. The pathway for generating these peptides begins in the cytoplasm, and the peptide-MHC I (pMHC I) repertoire is finalized in the endoplasmic reticulum. Recent studies show that the peptides for MHC I are customized by the ER aminopeptidase associated with antigen processing and by dynamic interactions within the MHC peptide-loading complex. Failure to customize the pMHC I repertoire has profound immunological consequences.
引用
收藏
页码:397 / 406
页数:10
相关论文
共 63 条
[1]   MHC class I molecules can direct proteolytic cleavage of antigenic precursors in the endoplasmic reticulum [J].
Brouwenstijn, N ;
Serwold, T ;
Shastri, N .
IMMUNITY, 2001, 15 (01) :95-104
[2]   26S proteasomes and immunoproteasomes produce mainly N-extended versions of an antigenic peptide [J].
Cascio, P ;
Hilton, C ;
Kisselev, AF ;
Rock, KL ;
Goldberg, AL .
EMBO JOURNAL, 2001, 20 (10) :2357-2366
[3]   The ER aminopeptidase, ERAN1, trims precursors to lengths of MHC class I peptides by a "molecular ruler" mechanism [J].
Chang, SC ;
Momburg, F ;
Bhutani, N ;
Goldberg, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (47) :17107-17112
[4]   Two distinct proteolytic processes in the generation of a major histocompatibility complex class I-presented peptide [J].
Craiu, A ;
Akoplan, T ;
Goldberg, A ;
Rock, KL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (20) :10850-10855
[5]   Mechanisms of MHC class I-restricted antigen processing and cross-presentation [J].
Cresswell, P ;
Ackerman, AL ;
Giodini, A ;
Peaper, DR ;
Wearsch, PA .
IMMUNOLOGICAL REVIEWS, 2005, 207 :145-157
[6]   Assembly of MHC class I peptide complexes from the perspective of disulfide bond formation [J].
Dick, TP .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2004, 61 (05) :547-556
[7]   Disulfide bond isomerization and the assembly of MHC class I-Peptide complexes [J].
Dick, TP ;
Bangia, N ;
Peaper, DR ;
Cresswell, P .
IMMUNITY, 2002, 16 (01) :87-98
[8]   The optimization of peptide cargo bound to MHC class I molecules by the peptide-loading complex [J].
Elliott, T ;
Williams, A .
IMMUNOLOGICAL REVIEWS, 2005, 207 :89-99
[9]   CELLULAR PEPTIDE COMPOSITION GOVERNED BY MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I MOLECULES [J].
FALK, K ;
ROTZSCHKE, O ;
RAMMENSEE, HG .
NATURE, 1990, 348 (6298) :248-251
[10]   ALLELE-SPECIFIC MOTIFS REVEALED BY SEQUENCING OF SELF-PEPTIDES ELUTED FROM MHC MOLECULES [J].
FALK, K ;
ROTZSCHKE, O ;
STEVANOVIC, S ;
JUNG, G ;
RAMMENSEE, HG .
NATURE, 1991, 351 (6324) :290-296