Modulation of the antigen transport machinery TAP by friends and enemies

被引:43
作者
Abele, R [1 ]
Tampé, R [1 ]
机构
[1] Goethe Univ Frankfurt, Inst Biochem, Bioctr, D-60439 Frankfurt, Germany
关键词
ABC transporter; antigen presentation; herpes virus; membrane transport; peptide-loading complex; transporter associated with antigen processing; tumor progression; viral escape;
D O I
10.1016/j.febslet.2005.11.048
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transporter associated with antigen processing (TAP) is a key factor of the major histocompatibility complex (MHC) class I antigen presentation pathway. This ABC transporter translocates peptides derived mainly from proteasomal degradation from the cytosol into the ER lumen for loading onto MHC class I molecules. Manifold mechanisms have evolved to regulate TAP activity. During infection, TAP expression is upregulated by interferon-gamma. Furthermore, the assembly and stability of the transport complex is promoted by various auxiliary factors. However, tumors and viruses have developed sophisticated strategies to escape the immune surveillance by suppressing TAP function. The activity of TAP can be impaired on the transcriptional or translational level, by enhanced degradation or by inhibition of peptide translocation. In this review, we briefly summarize existing data concerning the regulation of the TAP complex. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1156 / 1163
页数:8
相关论文
共 100 条
[1]   Function of the transport complex TAP in cellular immune recognition [J].
Abele, R ;
Tampé, R .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1999, 1461 (02) :405-419
[2]   Characterization of the protein encoded by gene UL49A of herpes simplex virus type 1 [J].
Adams, R ;
Cunningham, C ;
Davison, MD ;
MacLean, CA ;
Davison, AJ .
JOURNAL OF GENERAL VIROLOGY, 1998, 79 :813-823
[3]   The ER-luminal domain of the HCMV glycoprotein US6 inhibits peptide translocation by TAP [J].
Ahn, K ;
Gruhler, A ;
Galocha, B ;
Jones, TR ;
Wiertz, EJHJ ;
Ploegh, HL ;
Peterson, PA ;
Yang, Y ;
Fruh, K .
IMMUNITY, 1997, 6 (05) :613-621
[4]   Molecular mechanism and species specificity of TAP inhibition by herpes simplex virus protein ICP47 [J].
Ahn, K ;
Meyer, TH ;
Uebel, S ;
Sempe, P ;
Djaballah, H ;
Yang, Y ;
Peterson, PA ;
Fruh, K ;
Tampe, R .
EMBO JOURNAL, 1996, 15 (13) :3247-3255
[5]   TAP expression provides a general method for improving the recognition of malignant cells in vivo [J].
Alimonti, J ;
Zhang, QJ ;
Gabathuler, R ;
Reid, G ;
Chen, SS ;
Jefferies, WA .
NATURE BIOTECHNOLOGY, 2000, 18 (05) :515-520
[6]   IMPAIRED INTRACELLULAR-TRANSPORT OF CLASS-I MHC ANTIGENS AS A POSSIBLE MEANS FOR ADENOVIRUSES TO EVADE IMMUNE SURVEILLANCE [J].
ANDERSSON, M ;
PAABO, S ;
NILSSON, T ;
PETERSON, PA .
CELL, 1985, 43 (01) :215-222
[7]   EVIDENCE THAT TRANSPORTERS ASSOCIATED WITH ANTIGEN-PROCESSING TRANSLOCATE A MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I-BINDING PEPTIDE INTO THE ENDOPLASMIC-RETICULUM IN AN ATP-DEPENDENT MANNER [J].
ANDROLEWICZ, MJ ;
ANDERSON, KS ;
CRESSWELL, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (19) :9130-9134
[8]   Stoichiometric tapasin interactions in the catalysis of major histocompatibility complex class I molecule assembly [J].
Bangia, N ;
Cresswell, P .
IMMUNOLOGY, 2005, 114 (03) :346-353
[9]  
Bangia N, 1999, EUR J IMMUNOL, V29, P1858, DOI 10.1002/(SICI)1521-4141(199906)29:06<1858::AID-IMMU1858>3.0.CO
[10]  
2-C