A structural perspective on MHC class I recognition by killer cell immunoglobulin-like receptors

被引:144
作者
Boyington, JC [1 ]
Sun, PD [1 ]
机构
[1] NIAID, Struct Immunol Sect, Immunogenet Lab, NIH, Rockville, MD 20852 USA
关键词
NK cell receptors; receptor recognition; allotype specificity; KIR; HLA-C;
D O I
10.1016/S0161-5890(02)00030-5
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
Killer cell immunoglobulin-like receptors (KIR) play a critical role in the regulation of natural killer (NK) cell activity through their recognition of class I MHC Molecules expressed on target cells. KIR recognition provides vital information to NK cells about whether a target cell should be lysed or spared. Understanding the molecular mechanism of this recognition has remained a strong focus of investigation. This has resulted in the crystal structures of several members of the KIR family and more recently the determinations of the three dimensional structures of KlR2DL2 and KIR2DL1 complexed with their respective ligands. HLA-Cw3 and HLA-Cw4. A strong structural conservation has been revealed both in the receptor design and in the overall mode of KIR binding to class I molecules. Nevertheless, distinct differences in the receptor binding sites allow for high specificity between ligands. Furthermore, unexpected similarities with T-cell receptor (TCR) recognition of MHC molecules are also observed. The detailed interactions between KIR and HLA-C Molecules and their functional implications will be reviewed here. Published by Elsevier Science Ltd.
引用
收藏
页码:1007 / 1021
页数:15
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