Automated generation and evaluation of specific MHC binding predictive tools:: ARB matrix applications

被引:208
作者
Bui, HH
Sidney, J
Peters, B
Sathiamurthy, M
Sinichi, A
Purton, KA
Mothé, BR
Chisari, FV
Watkins, DI
Sette, A
机构
[1] La Jolla Inst Allergy & Immunol, Div Vaccine Discovery, San Diego, CA 92109 USA
[2] Scripps Res Inst, Div Expt Pathol, La Jolla, CA 92037 USA
[3] Univ Wisconsin, Wisconsin Reg Primate Ctr, Madison, WI 53719 USA
关键词
MHC; binding prediction; computer algorithms; automated tool evaluation; Web server;
D O I
10.1007/s00251-005-0798-y
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Prediction of which peptides can bind major histocompatibility complex (MHC) molecules is commonly used to assist in the identification of T cell epitopes. However, because of the large numbers of different MHC molecules of interest, each associated with different predictive tools, tool generation and evaluation can be a very resource intensive task. A methodology commonly used to predict MHC binding affinity is the matrix or linear coefficients method. Herein, we described Average Relative Binding (ARB) matrix methods that directly predict IC50 values allowing combination of searches involving different peptide sizes and alleles into a single global prediction. A computer program was developed to automate the generation and evaluation of ARB predictive tools. Using an in-house MHC binding database, we generated a total of 85 and 13 MHC class I and class II matrices, respectively. Results from the automated evaluation of tool efficiency are presented. We anticipate that this automation framework will be generally applicable to the generation and evaluation of large numbers of MHC predictive methods and tools, and will be of value to centralize and rationalize the process of evaluation of MHC predictions. MHC binding predictions based on ARB matrices were made available at http://www.epitope.liai.org:8080/matrix web server.
引用
收藏
页码:304 / 314
页数:11
相关论文
共 31 条
[1]   SVM based method for predicting HLA-DRB1*0401 binding peptides in an antigen sequence [J].
Bhasin, M ;
Raghava, GPS .
BIOINFORMATICS, 2004, 20 (03) :421-423
[2]   Specific and general HLA-DR binding motifs:: Comparison of algorithms [J].
Borrás-Cuesta, F ;
Golvano, JJ ;
García-Granero, M ;
Sarobe, P ;
Riezu-Boj, JI ;
Huarte, E ;
Lasarte, JJ .
HUMAN IMMUNOLOGY, 2000, 61 (03) :266-278
[3]  
Brusic V, 1997, ISMB-97 - FIFTH INTERNATIONAL CONFERENCE ON INTELLIGENT SYSTEMS FOR MOLECULAR BIOLOGY, PROCEEDINGS, P75
[4]   Sensitive quantitative predictions of peptide-MHC binding by a 'Query by Committee' artificial neural network approach [J].
Buus, S ;
Lauemoller, SL ;
Worning, P ;
Kesmir, C ;
Frimurer, T ;
Corbet, S ;
Fomsgaard, A ;
Hilden, J ;
Holm, A ;
Brunak, S .
TISSUE ANTIGENS, 2003, 62 (05) :378-384
[5]  
DAVENPORT MP, 1995, IMMUNOGENETICS, V42, P392
[6]   Prediction of MHC class I binding peptides, using SVMHC -: art. no. 25 [J].
Dönnes, P ;
Elofsson, A .
BMC BIOINFORMATICS, 2002, 3 (1)
[7]   Identification of Plasmodium falciparum antigens by antigenic analysis of genomic and proteomic data [J].
Doolan, DL ;
Southwood, S ;
Freilich, DA ;
Sidney, J ;
Graber, NL ;
Shatney, L ;
Bebris, L ;
Florens, L ;
Dobano, C ;
Witney, AA ;
Appella, E ;
Hoffman, SL ;
Yates, JR ;
Carucci, DJ ;
Sette, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (17) :9952-9957
[8]   Two complementary methods for predicting peptides binding major histocompatibility complex molecules [J].
Gulukota, K ;
Sidney, J ;
Sette, A ;
DeLisi, C .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 267 (05) :1258-1267
[9]   PRECISE PREDICTION OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II PEPTIDE INTERACTION BASED ON PEPTIDE SIDE-CHAIN SCANNING [J].
HAMMER, J ;
BONO, E ;
GALLAZZI, F ;
BELUNIS, C ;
NAGY, Z ;
SINIGAGLIA, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (06) :2353-2358
[10]   Two distinct HLA-A*0101-specific submotifs illustrate alternative peptide binding modes [J].
Kondo, A ;
Sidney, J ;
Southwood, S ;
delGuercio, MF ;
Appella, E ;
Sakamoto, H ;
Grey, HM ;
Celis, E ;
Chesnut, RW ;
Kubo, RT ;
Sette, A .
IMMUNOGENETICS, 1997, 45 (04) :249-258