Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1410468 | Journal of Molecular Structure | 2009 | 4 Pages |
Abstract
A set of 70 peptides with affinity for the class I MHC HLA-Aâ0201 molecule was subjected to quantitative structure-affinity relationship studies based on the SCORE function with good results (r2Â =Â 0.6982, RMSÂ =Â 0.280). Then the 'leave-one-out' cross-validation (LOO-CV) and an outer test set including 18 outer samples were used to validate the QSAR model. The results of the LOO-CV were q2Â =Â 0.6188, RMSÂ =Â 0.315, and the results of outer test set were r2Â =Â 0.5633, RMSÂ =Â 0.2292. All these show that the QSAR model has good predictability. Statistical analysis showed that the hydrophobic and hydrogen bond interaction played a significant role in peptide-MHC molecule binding. The study also provided useful information for structure modification of CTL epitope, and laid theoretical base for molecular design of therapeutic vaccine.
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Authors
Yun-sheng Xu, Yong Lin, Bo Zhu, Zhi-hua Lin,