Literature DB >> 15592665

Peptide-binding motif of HLA-A*6603.

Christina Bade-Doeding1, Britta Eiz-Vesper, Constanca Figueiredo, Axel Seltsam, Holger-Andreas Elsner, Rainer Blasczyk.   

Abstract

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.

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Year:  2004        PMID: 15592665     DOI: 10.1007/s00251-004-0747-1

Source DB:  PubMed          Journal:  Immunogenetics        ISSN: 0093-7711            Impact factor:   2.846


  18 in total

1.  The HLA-A*6601 peptide motif: prediction by pocket structure and verification by peptide analysis.

Authors:  F H Seeger; M Schirle; J Gatfield; D Arnold; W Keilholz; P Nickolaus; H G Rammensee; S Stevanović
Journal:  Immunogenetics       Date:  1999-06       Impact factor: 2.846

2.  Differences in the recognition by CTL of peptides presented by the HLA-B*4402 and the HLA-B*4403 molecules which differ by a single amino acid.

Authors:  J Herman; V Jongeneel; D Kuznetsov; P G Coulie
Journal:  Tissue Antigens       Date:  1999-02

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Authors:  S Hausmann; W E Biddison; K J Smith; Y H Ding; D N Garboczi; U Utz; D C Wiley; K W Wucherpfennig
Journal:  J Immunol       Date:  1999-05-01       Impact factor: 5.422

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Authors:  M Matsumura; D H Fremont; P A Peterson; I A Wilson
Journal:  Science       Date:  1992-08-14       Impact factor: 47.728

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Journal:  J Mol Biol       Date:  1991-05-20       Impact factor: 5.469

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Authors:  T Dumrese; S Stevanović; F H Seeger; N Yamada; Y Ishikawa; K Tokunaga; M Takiguchi; H Rammensee
Journal:  Immunogenetics       Date:  1998-10       Impact factor: 2.846

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Journal:  Immunol Rev       Date:  1979       Impact factor: 12.988

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10.  Characterization of natural peptide ligands for HLA-B*4402 and -B*4403: implications for peptide involvement in allorecognition of a single amino acid change in the HLA-B44 heavy chain.

Authors:  K Fleischhauer; D Avila; F Vilbois; C Traversari; C Bordignon; H J Wallny
Journal:  Tissue Antigens       Date:  1994-11
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  2 in total

1.  The impact of human leukocyte antigen (HLA) micropolymorphism on ligand specificity within the HLA-B*41 allotypic family.

Authors:  Christina Bade-Döding; Alex Theodossis; Stephanie Gras; Lars Kjer-Nielsen; Britta Eiz-Vesper; Axel Seltsam; Trevor Huyton; Jamie Rossjohn; James McCluskey; Rainer Blasczyk
Journal:  Haematologica       Date:  2010-10-07       Impact factor: 9.941

2.  A modular concept of HLA for comprehensive peptide binding prediction.

Authors:  David S DeLuca; Barbara Khattab; Rainer Blasczyk
Journal:  Immunogenetics       Date:  2006-11-22       Impact factor: 2.846

  2 in total

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