Evolutionarily conserved amino acids that control TCR-MHC interaction

被引:208
作者
Marrack, Philippa [1 ,2 ,3 ,4 ]
Scott-Browne, James P. [2 ]
Dai, Shaodong [1 ,2 ]
Gapin, Laurent [2 ]
Kappler, John W. [1 ,2 ,4 ,5 ,6 ]
机构
[1] Univ Colorado, Denver Hlth Sci Ctr, Howard Hughes Med Inst, Denver, CO 80202 USA
[2] Univ Colorado, Denver Hlth Sci Ctr, Natl Jewish Med & Res Ctr, Integrated Dept Immunol, Denver, CO 80202 USA
[3] Univ Colorado, Denver Hlth Sci Ctr, Dept Biochem & Mol Genet, Denver, CO 80202 USA
[4] Univ Colorado, Denver Hlth Sci Ctr, Dept Med, Denver, CO 80202 USA
[5] Univ Colorado, Denver Hlth Sci Ctr, Dept Pharmacol, Denver, CO 80202 USA
[6] Univ Colorado, Denver Hlth Sci Ctr, Program Biomol Struct, Denver, CO 80202 USA
关键词
T cell receptor; major histocompatibility complex; evolution; conserved interactions; tolerance; selection;
D O I
10.1146/annurev.immunol.26.021607.090421
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The rules for the conserved reaction of alpha beta T cell receptors (TCRs) with major histocompatibility complex (MHC) proteins plus peptides are poorly understood, probably because thymocytes hearing TCRs with the strongest MHC reactivity are lost by negative selection. Thus, only TCRs with an attenuated ability to react with MHC appear on mature T cells. Also, the interaction sites between TCRs and MHC may be inherently flexible and hence difficult to spot. We reevaluated contacts between TCRs and MHC in the solved structures of their complexes with these points in mind. Relatively conserved amino acids in the TCR complementarity-determining regions (CDR) 1 and CDR2 are often used to bind exposed areas of the MHC alpha-helices. These areas are exposed because of small amino acids that allow somewhat flexible binding of the TCRs. The TCR amino acids involved are specific to families of variable (V) regions and to some extent different rules may govern the recognition of MHCI versus MHCII.
引用
收藏
页码:171 / 203
页数:33
相关论文
共 125 条
[51]   Interface-disrupting amino acids establish specificity between T cell receptors and complexes of major histocompatibility complex and peptide [J].
Huseby, Eric S. ;
Crawford, Frances ;
White, Janice ;
Marrack, Philippa ;
Kappler, John W. .
NATURE IMMUNOLOGY, 2006, 7 (11) :1191-1199
[52]   How the T cell repertoire becomes peptide and MHC specific [J].
Huseby, ES ;
White, J ;
Crawford, F ;
Vass, T ;
Becker, D ;
Pinilla, C ;
Marrack, P ;
Kappler, JW .
CELL, 2005, 122 (02) :247-260
[53]   Negative selection imparts peptide specificity to the mature T cell repertoire [J].
Huseby, ES ;
Crawford, F ;
White, J ;
Kappler, J ;
Marrack, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (20) :11565-11570
[54]   The repertoire of T cells shaped by a single MHC/peptide ligand [J].
Ignatowicz, L ;
Kappler, J ;
Marrack, P .
CELL, 1996, 84 (04) :521-529
[55]   STRUCTURE, DIVERSITY, AND EVOLUTION OF THE T-CELL RECEPTOR VB GENE REPERTOIRE IN PRIMATES [J].
JAEGER, EEM ;
BONTROP, RE ;
LANCHBURY, JS .
IMMUNOGENETICS, 1994, 40 (03) :184-191
[56]  
JERNE N K, 1971, European Journal of Immunology, V1, P1, DOI 10.1002/eji.1830010102
[57]   T-CELL TOLERANCE BY CLONAL ELIMINATION IN THE THYMUS [J].
KAPPLER, JW ;
ROEHM, N ;
MARRACK, P .
CELL, 1987, 49 (02) :273-280
[58]   ANTIGEN-INDUCIBLE, H-2-RESTRICTED, INTERLEUKIN-2-PRODUCING T-CELL HYBRIDOMAS - LACK OF INDEPENDENT ANTIGEN AND H-2 RECOGNITION [J].
KAPPLER, JW ;
SKIDMORE, B ;
WHITE, J ;
MARRACK, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1981, 153 (05) :1198-1214
[59]   CD1d-restricted and TCR-mediated activation of V(alpha)14 NKT cells by glycosylceramides [J].
Kawano, T ;
Cui, JQ ;
Koezuka, Y ;
Toura, I ;
Kaneko, Y ;
Motoki, K ;
Ueno, H ;
Nakagawa, R ;
Sato, H ;
Kondo, E ;
Koseki, H ;
Taniguchi, M .
SCIENCE, 1997, 278 (5343) :1626-1629
[60]   Recognition of bacterial glycosphingolipids by natural killer T cells [J].
Kinjo, Y ;
Wu, D ;
Kim, GS ;
Xing, GW ;
Poles, MA ;
Ho, DD ;
Tsuji, M ;
Kawahara, K ;
Wong, CH ;
Kronenberg, M .
NATURE, 2005, 434 (7032) :520-525