MHC-BPS: MHC-binder prediction server for identifying peptides of flexible lengths from sequence-derived physicochemical properties

被引:20
作者
Cui, Juan
Han, Lian Yi
Lin, Hong Huang
Tang, Zhi Qun
Jiang, Li
Cao, Zhi Wei
Chen, Yu Zong [1 ]
机构
[1] Natl Univ Singapore, Dept Computat Sci, Singapore 117543, Singapore
[2] Natl Univ Singapore, Dept Pharm, Bioinformat & Drug Design Grp, Singapore 117543, Singapore
[3] Shanghai Ctr Bioinformat Technol, Shanghai 200235, Peoples R China
关键词
MHC-binding peptide; epitopes; SVM;
D O I
10.1007/s00251-006-0117-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Major histocompatibility complex (MHC)-binding peptides are essential for antigen recognition by T-cell receptors and are being explored for vaccine design. Computational methods have been developed for predicting MHC-binding peptides of fixed lengths, based on the training of relatively few non-binders. It is desirable to introduce methods applicable for peptides of flexible lengths and trained by using more diverse sets of non-binders. MHC-BPS is a web-based MHC-binder prediction server that uses support vector machines for predicting peptide binders of flexible lengths for 18 MHC class I and 12 class II alleles from sequence-derived physicochemical properties, which were trained by using 4,208 similar to 3,252 binders and 234,333 similar to 168,793 non-binders, and evaluated by an independent set of 545 similar to 476 binders and 110,564 similar to 84,430 non-binders. The binder prediction accuracies are 86 similar to 99% for 25 and 70 similar to 80% for five alleles, and the non-binder accuracies are 96 similar to 99% for 30 alleles. A screening of HIV-1 genome identifies 0.01 similar to 5% and 5 similar to 8% of the constituent peptides as binders for 24 and 6 alleles, respectively, including 75 similar to 100% of the known epitopes. This method correctly predicts 73.3% of the 15 newly published epitopes in the last 4 months of 2005.
引用
收藏
页码:607 / 613
页数:7
相关论文
共 40 条
[1]   A structure-based algorithm to predict potential binding peptides to MHC molecules with hydrophobic binding pockets [J].
Altuvia, Y ;
Sette, A ;
Sidney, J ;
Southwood, S ;
Margalit, H .
HUMAN IMMUNOLOGY, 1997, 58 (01) :1-11
[2]   Prediction of CTL epitopes using QM, SVM and ANN techniques [J].
Bhasin, M ;
Raghava, GPS .
VACCINE, 2004, 22 (23-24) :3195-3204
[3]   Discovery of promiscuous HLA-II-restricted T cell epitopes with TEPITOPE [J].
Bian, HJ ;
Hammer, J .
METHODS, 2004, 34 (04) :468-475
[4]   A tutorial on Support Vector Machines for pattern recognition [J].
Burges, CJC .
DATA MINING AND KNOWLEDGE DISCOVERY, 1998, 2 (02) :121-167
[5]   SVM-Prot: web-based support vector machine software for functional classification of a protein from its primary sequence [J].
Cai, CZ ;
Han, LY ;
Ji, ZL ;
Chen, X ;
Chen, YZ .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3692-3697
[6]   Engineering immunogenic consensus T helper epitopes for a cross-clade HIV vaccine [J].
De Groot, AS ;
Bishop, EA ;
Khan, B ;
Lally, M ;
Marcon, L ;
Franco, J ;
Mayer, KH ;
Carpenter, CCJ ;
Martin, W .
METHODS, 2004, 34 (04) :476-487
[7]   Mapping cross-clade HIV-1 vaccine epitopes using a bioinformatics approach [J].
De Groot, AS ;
Jesdale, B ;
Martin, W ;
Saint Aubin, C ;
Sbai, H ;
Bosma, A ;
Lieberman, J ;
Skowron, G ;
Mansourati, F ;
Mayer, KH .
VACCINE, 2003, 21 (27-30) :4486-4504
[8]   Prediction of MHC class I binding peptides, using SVMHC -: art. no. 25 [J].
Dönnes, P ;
Elofsson, A .
BMC BIOINFORMATICS, 2002, 3 (1)
[9]   Integrated modeling of the major events in the MHC class I antigen processing pathway [J].
Dönnes, P ;
Kohlbacher, O .
PROTEIN SCIENCE, 2005, 14 (08) :2132-2140
[10]   Coupling in silico and in vitro analysis of peptide-MHC binding: A bioinformatic approach enabling prediction of superbinding peptides and anchorless epitopes [J].
Doytchinova, IA ;
Walshe, VA ;
Jones, NA ;
Gloster, SE ;
Borrow, P ;
Flower, DR .
JOURNAL OF IMMUNOLOGY, 2004, 172 (12) :7495-7502