PREDICTION OF BINDING TO MHC CLASS-I MOLECULES

被引:63
作者
ADAMS, HP
KOZIOL, JA
机构
[1] Division of Biomathematics, Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA 92037, Mail Drop SBR-7
关键词
HLA; MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I; MAJOR HISTOCOMPATIBILITY COMPLEX CLASS II; T CELL; NEURAL NETWORK (COMPUTER);
D O I
10.1016/0022-1759(95)00111-M
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The binding of antigenic peptide sequences to major histocompatibility complex (MHC) molecules is a prerequisite for stimulation of cytotoxic T cell responses. Neural networks are here used to predict the binding capacity of polypeptides to MHC class I molecules encoded by the gene HLA-A* 0201. Given a large database of 552 nonamers and 486 decamers and their known binding capacities, the neural networks achieve a predictive hit rate of 0.78 for classifying peptides which might induce an immune response (good or intermediate binders) vs. those which cannot (weak or non-binders). The neural nets also depict specific motifs for different binding capacities. This approach is in principle applicable to all MHC class I and II molecules, given a suitable set of known binding capacities. The trained networks can then be used to perform a systematic search through all pathogen or tumor antigen protein sequences for potential cytotoxic T lymphocyte epitopes.
引用
收藏
页码:181 / 190
页数:10
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