Peptide-binding motif of HLA-A*6603

被引:5
作者
Bade-Doeding, C
Eiz-Vesper, B
Figueiredo, C
Seltsam, A
Elsner, HA
Blasczyk, R
机构
[1] Hannover Med Sch, Dept Transfus Med, D-30625 Hannover, Germany
[2] MMD Med Mol Diagnost GmbH, Dresden, Germany
关键词
HLA-A*6603; peptides; peptide motif; auxiliary anchor; pockets;
D O I
10.1007/s00251-004-0747-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The peptide motif of HLA-A*6603 was determined and compared with the available data on the peptide motifs of A*6601 and A*6602. A*6601 differs from A*6602 by two amino acids at positions 90 (Asp90Ala; outer loop) and 163 (Arg163Glu; pocket A). A*6603 differs from A*6601 and A*6602 by a single amino-acid exchange at position 70 (His70Gln; pockets A, B and C). No significant differences were found between the A*6602 and A*6603 peptide motifs suggesting that the Gln70His variation is of minor importance. However, the auxiliary anchors at position P1 of peptides bound by A*6601 (polar/acidic: Asp, Glu) and A*6602/6603 (polar/neutral: Ser) had striking differences. This finding may be best explained by the Arg163Glu substitution that results in a shift towards higher acidity in pocket A of A*6602/6603, apparently leading to the loss of preference for acidic auxiliary anchors. The similarity of A*6602 and A*6603 peptide motifs suggests low allogenicity when mismatched in stem cell transplantation. Inversely, the differences in A*6601 versus A*6602/6603 peptide motifs suggest that mismatches will have a higher allogenicity. These data will contribute to both assessing permissive mismatches in the A*66 group and weighting the impact of this individual amino-acid variation for matching and peptide binding algorithms.
引用
收藏
页码:769 / 772
页数:4
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