Crystal structure of HLA-DQ0602 that protects against type 1 diabetes and confers strong susceptibility to narcolepsy

被引:110
|
作者
Siebold, C
Hansen, BE
Wyer, JR
Harlos, K
Esnouf, RE
Svejgaard, A
Bell, JI
Strominger, JL
Jones, EY
Fugger, L
机构
[1] Univ Oxford, Div Struct biol, Oxford OX3 7BN, England
[2] Aarhus Univ Hosp, Dept Clin Immunol, Skejby Sygehus, DK-8200 Aarhus N, Denmark
[3] Copenhagen Univ Hosp, Rigshosp, Dept Clin Immunol, DK-2200 Copenhagen N, Denmark
[4] Univ Oxford, John Radcliffe Hosp, Off Regius Prof, Oxford OX3 9DS, England
[5] Univ Oxford, MRC, Human Immunol Unit, Weatherall Inst Mol Med, Oxford OX3 9DS, England
[6] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
D O I
10.1073/pnas.0308458100
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
The MHC class II molecule DQ0602 confers strong susceptibility to narcolepsy but dominant protection against type 1 diabetes. The crystal structure of DQ0602 reveals the molecular features underlying these contrasting genetic properties. Structural comparisons to homologous DQ molecules with differential disease associations highlight a previously unrecognized interplay between the volume of the P6 pocket and the specificity of the P9 pocket, which implies that presentation of an expanded peptide repertoire is critical for dominant protection against type 1 diabetes. In narcolepsy, the volume of the P4 pocket appears central to the susceptibility, suggesting that the presentation of a specific peptide population plays a major role.
引用
收藏
页码:1999 / 2004
页数:6
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