SUBSETS OF HLA-DR1 MOLECULES DEFINED BY SEB AND TSST-1 BINDING

被引:85
作者
THIBODEAU, J
CLOUTIER, I
LAVOIE, PM
LABRECQUE, N
MOURAD, W
JARDETZKY, T
SEKALY, RP
机构
[1] CLIN RES INST MONTREAL,IMMUNOL LAB,MONTREAL H2W 1R7,PQ,CANADA
[2] UNIV MONTREAL,FAC MED,DEPT IMMUNOL & MICROBIOL,MONTREAL,PQ,CANADA
[3] MCGILL UNIV,SCH MED,DEPT MICROBIOL & IMMUNOL,MONTREAL H3A 2B4,PQ,CANADA
[4] CHU LAVAL,DEPT IMMUNOL & RHUMATOL,ST FOY G1V 4G2,PQ,CANADA
[5] HARVARD UNIV,DEPT BIOCHEM & MOLEC BIOL,CAMBRIDGE,MA 02138
关键词
D O I
10.1126/science.7997881
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Superantigens bind to major histocompatibility complex class II molecules on antigen-presenting cells and stimulate T cells. Staphylococcus aureus enterotoxin B (SEB) and toxic shock syndrome toxin-1 (TSST-1) bind to the same region of human lymphocyte antigen (HL4)-DR1 but do not compete with each other, which indicates that they bind to different subsets of DR1 molecules. Here, a mutation in the peptide-binding groove disrupted the SEB and TSST-1 binding sites, which suggests that peptides can influence the interaction with bacterial toxins. in support of this, the expression of the DR1 molecule in various cell types differentially affected the binding of these toxins.
引用
收藏
页码:1874 / 1878
页数:5
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