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人类白细胞抗原(HLA)-DRB1*15:01和HLA-DRB5*01:01呈现互补的肽库。

Human Leukocyte Antigen (HLA)-DRB1*15:01 and HLA-DRB5*01:01 Present Complementary Peptide Repertoires.

作者信息

Scholz Erika Margaret, Marcilla Miguel, Daura Xavier, Arribas-Layton David, James Eddie A, Alvarez Iñaki

机构信息

Institut de Biotecnologia i de Biomedicina, Universitat Autònoma de Barcelona, Bellaterra, Spain.

Immunology Unit, Department of Cell Biology, Physiology and Immunology, Universitat Autònoma de Barcelona, Bellaterra, Spain.

出版信息

Front Immunol. 2017 Aug 21;8:984. doi: 10.3389/fimmu.2017.00984. eCollection 2017.

DOI:10.3389/fimmu.2017.00984
PMID:28871256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5566978/
Abstract

Human leukocyte antigen (HLA)-DR15 is a haplotype associated with multiple sclerosis. It contains the two DRB* genes * (DR2b) and * (DR2a). The reported anchor motif of the corresponding HLA-DR molecules was determined in 1994 based on a small number of peptide ligands and binding assays. DR2a could display a set of peptides complementary to that presented by DR2b or, alternatively, a similar peptide repertoire but recognized in a different manner by T cells. It is known that DR2a and DR2b share some peptide ligands, although the degree of similarity of their associated peptidomes remains unclear. In addition, the contribution of each molecule to the global peptide repertoire presented by the HLA-DR15 haplotype has not been evaluated. We used mass spectrometry to analyze the peptide pools bound to DR2a and DR2b, identifying 169 and 555 unique peptide ligands of DR2a and DR2b, respectively. The analysis of these sets of peptides allowed the refinement of the corresponding binding motifs revealing novel anchor residues that had been overlooked in previous analyses. Moreover, the number of shared ligands between both molecules was low, indicating that DR2a and DR2b present complementary peptide repertoires to T cells. Finally, our analysis suggests that, quantitatively, both molecules contribute to the peptide repertoire presented by cells expressing the HLA-DR15 haplotype.

摘要

人类白细胞抗原(HLA)-DR15是一种与多发性硬化症相关的单倍型。它包含两个DRB基因(DR2b)和*(DR2a)。相应HLA-DR分子的已报道锚定基序是在1994年基于少量肽配体和结合试验确定的。DR2a可能展示一组与DR2b所呈递的肽互补的肽,或者展示一组类似的肽库,但被T细胞以不同方式识别。已知DR2a和DR2b共享一些肽配体,尽管它们相关肽组的相似程度仍不清楚。此外,每个分子对HLA-DR15单倍型所呈递的整体肽库的贡献尚未得到评估。我们使用质谱分析与DR2a和DR2b结合的肽池,分别鉴定出DR2a和DR2b的169个和555个独特肽配体。对这些肽组的分析使得能够完善相应的结合基序,揭示先前分析中被忽视的新锚定残基。此外,两个分子之间共享配体的数量很少,表明DR2a和DR2b向T细胞呈递互补的肽库。最后,我们的分析表明,从数量上看,两个分子都对表达HLA-DR15单倍型的细胞所呈递的肽库有贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/7b17f6ca43c9/fimmu-08-00984-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/b276ba9634ac/fimmu-08-00984-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/8582dff0e768/fimmu-08-00984-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/e742f2185962/fimmu-08-00984-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/4e6fd72fb752/fimmu-08-00984-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/7b17f6ca43c9/fimmu-08-00984-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/b276ba9634ac/fimmu-08-00984-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/8582dff0e768/fimmu-08-00984-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/e742f2185962/fimmu-08-00984-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/4e6fd72fb752/fimmu-08-00984-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdff/5566978/7b17f6ca43c9/fimmu-08-00984-g005.jpg

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