Abstract
Computer models usefully complement experimentation in the efficient discovery of MHC-binding peptides and T-cell epitopes, and have been applied successfully to predict T-cell epitopes in infectious disease, cancer, autoimmunity and allergy. Prediction methods include binding motifs, quantitative matrices, various artificial intelligence techniques and molecular modelling. Computational modelling should be performed according to strict standards, requiring careful data selection for model building, followed by adequate testing and validation. Many web-based databases and binding prediction programs are now available. Although certain prediction programs are reasonably accurate, at least for some MHC alleles, one cannot guarantee that all models produce results of adequate predictivity and therefore these prediction results should be used with care.
Original language | English |
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Pages (from-to) | 18-23 |
Number of pages | 6 |
Journal | Drug Discovery Today: BIOSILICO |
Volume | 2 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1 Jan 2004 |
Externally published | Yes |
ASJC Scopus subject areas
- Drug Discovery