Bergmann Tobias, Lindvall Mikaela, Moore Erin, Moore Eugene, Sidney John, Miller Donald, Tallmadge Rebecca L, Myers Paisley T, Malaker Stacy A, Shabanowitz Jeffrey, Osterrieder Nikolaus, Peters Bjoern, Hunt Donald F, Antczak Douglas F, Sette Alessandro
Institut für Virologie, Freie Universität Berlin, 14163, Berlin, Germany.
Department of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA, 92037, USA.
Immunogenetics. 2017 May;69(5):351-358. doi: 10.1007/s00251-017-0978-6. Epub 2017 Mar 18.
Quantitative peptide-binding motifs of MHC class I alleles provide a valuable tool to efficiently identify putative T cell epitopes. Detailed information on equine MHC class I alleles is still very limited, and to date, only a single equine MHC class I allele, Eqca-100101 (ELA-A3 haplotype), has been characterized. The present study extends the number of characterized ELA class I specificities in two additional haplotypes found commonly in the Thoroughbred breed. Accordingly, we here report quantitative binding motifs for the ELA-A2 allele Eqca-1600101 and the ELA-A9 allele Eqca-100201. Utilizing analyses of endogenously bound and eluted ligands and the screening of positional scanning combinatorial libraries, detailed and quantitative peptide-binding motifs were derived for both alleles. Eqca-1600101 preferentially binds peptides with aliphatic/hydrophobic residues in position 2 and at the C-terminus, and Eqca-100201 has a preference for peptides with arginine in position 2 and hydrophobic/aliphatic residues at the C-terminus. Interestingly, the Eqca-1600101 motif resembles that of the human HLA A02-supertype, while the Eqca-1*00201 motif resembles that of the HLA B27-supertype and two macaque class I alleles. It is expected that the identified motifs will facilitate the selection of candidate epitopes for the study of immune responses in horses.
MHC I类等位基因的定量肽结合基序为有效鉴定假定的T细胞表位提供了一个有价值的工具。关于马MHC I类等位基因的详细信息仍然非常有限,迄今为止,仅鉴定了一个马MHC I类等位基因Eqca-100101(ELA-A3单倍型)。本研究扩展了在纯种马中常见的另外两种单倍型中已鉴定的ELA I类特异性的数量。因此,我们在此报告ELA-A2等位基因Eqca-1600101和ELA-A9等位基因Eqca-100201的定量结合基序。通过对内源性结合和洗脱配体的分析以及位置扫描组合文库的筛选,得出了这两个等位基因的详细定量肽结合基序。Eqca-1600101优先结合在第2位和C末端具有脂肪族/疏水残基的肽,而Eqca-100201则优先结合在第2位具有精氨酸且在C末端具有疏水/脂肪族残基的肽。有趣的是,Eqca-1600101基序类似于人类HLA A02超型的基序,而Eqca-1*00201基序类似于HLA B27超型和两个猕猴I类等位基因的基序。预计所鉴定的基序将有助于选择候选表位用于研究马的免疫反应。