BINDING MOTIFS PREDICT MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II-RESTRICTED EPITOPES IN THE SENDAI-VIRUS M-PROTEIN

被引:10
作者
COLE, GA
TAO, T
HOGG, TL
RYAN, KW
WOODLAND, DL
机构
[1] ST JUDE CHILDRENS RES HOSP, DEPT IMMUNOL, MEMPHIS, TN 38105 USA
[2] ST JUDE CHILDRENS RES HOSP, DEPT VIROL, MEMPHIS, TN 38105 USA
[3] UNIV TENNESSEE, DEPT PATHOL, MEMPHIS, TN 38163 USA
关键词
D O I
10.1128/JVI.69.12.8057-8060.1995
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Major histocompatibility complex (MHC) class I ligand motifs have been defined for a number of class I molecules and have been successfully used to identify class I-restricted cytotoxic T-cell epitopes. In contrast, the relative degeneracy of sequence motifs in naturally processed MHC class II ligands has suggested that they may be of more limited use. Here, we use a predicted I-A(b) ligand motif to identify antigenic peptides in the Sendai virus Enders strain matrix (M) protein. The entire coding sequence of the M protein was derived, and seven peptide sequences that contained the predicted I-A(b) motif were identified. Analysis of I-A(b)-restricted M-specific T-cell hybridomas for reactivity to these synthetic peptides identified two distinct epitopes. These data demonstrate that MHC class II motifs can be valuable in predicting T-cell epitopes.
引用
收藏
页码:8057 / 8060
页数:4
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