HLA CLASS-I SELF PEPTIDES ISOLATED FROM A T-CELL LEUKEMIA REVEAL THE ALLELE-SPECIFIC MOTIF OF HLA-B38

被引:9
作者
COLOVAI, AI
SUCIUFOCA, N
BAIULESCU, GE
HARRIS, PE
机构
[1] COLUMBIA UNIV,COLL PHYS & SURG,DEPT PATHOL,DIV IMMUNOGENET,NEW YORK,NY 10032
[2] UNIV BUCHAREST,FAC CHEM,DEPT ANALYT CHEM,BUCHAREST,ROMANIA
来源
TISSUE ANTIGENS | 1994年 / 44卷 / 02期
关键词
MHC; HLA-B38; ALLELE-SPECIFIC MOTIF; PEPTIDE SEQUENCING;
D O I
10.1111/j.1399-0039.1994.tb02361.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Naturally-processed self peptides bound to HLA class I molecules of a T-cell leukemia (HLA-A1, A31, B38, B58) were isolated for sequence analysis. Acid-eluted peptides were subjected to reversed-phase HPLC separation and single-fraction sequencing was performed by Edman degradation. The peptides were found to be mostly nonamers and could be grouped into three distinct structural motifs. One of the peptide groups consistently displayed histidine at position 2 and a bulky hydrophobic residue at the C-terminus (XHXPXXXXY/F). The only HLA class I structure expressed by this T-cell leukemia which is consistent with the binding of peptides carrying this sequence motif is HLA-B38. A peptide binding assay confirmed this assignment. HLA-B38 is present in 10-12% of the Jewish population and is associated with several autoimmune disorders. The HLA-B38 motif may be an important tool for identifying potential T-cell epitopes involved in these diseases and for designing peptide vaccines.
引用
收藏
页码:65 / 72
页数:8
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