Computational methods for prediction of T-cell epitopes - a framework for modelling, testing, and applications

被引:182
作者
Brusic, V
Bajic, VB
Petrovsky, N
机构
[1] Labs Informat Technol, Singapore 119613, Singapore
[2] Univ Canberra, Med Informat Ctr, Div Sci & Design, Bruce, ACT 2617, Australia
[3] Univ Western Cape, S African Natl Bioinformat Inst, Cape Town, South Africa
[4] Canberra Clin School, Natl Hlth Sci Ctr, Woden, ACT 2606, Australia
关键词
D O I
10.1016/j.ymeth.2004.06.006
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Computational models complement laboratory experimentation for efficient identification of MHC-binding peptides and T-cell epitopes. Methods for prediction of MHC-binding peptides include binding motifs, quantitative matrices, artificial neural networks, hidden Markov models, and molecular modelling. Models derived by these methods have been successfully used for prediction of T-cell epitopes in cancer, autoimmunity, infectious disease, and allergy. For maximum benefit, the use of computer models must be treated as experiments analogous to standard laboratory procedures and performed according to strict standards. This requires careful selection of data for model building, and adequate testing and validation. A range of web-based databases and MHC-binding prediction programs are available. Although some available prediction programs for particular MHC alleles have reasonable accuracy, there is no guarantee that all models produce good quality predictions. In this article, we present and discuss a framework for modelling, testing, and applications of computational methods used in predictions of T-cell epitopes. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:436 / 443
页数:8
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