TY - JOUR
T1 - MULTIPRED2
T2 - A computational system for large-scale identification of peptides predicted to bind to HLA supertypes and alleles
AU - Zhang, Guang Lan
AU - DeLuca, David S.
AU - Keskin, Derin B.
AU - Chitkushev, Lou
AU - Zlateva, Tanya
AU - Lund, Ole
AU - Reinherz, Ellis L.
AU - Brusic, Vladimir
N1 - Funding Information:
This work was supported by NIH grants U19 AI 57330 and U01 AI 90043 and a grant from DOD W81XWH-07-1-0080 .
PY - 2011/11/30
Y1 - 2011/11/30
N2 - MULTIPRED2 is a computational system for facile prediction of peptide binding to multiple alleles belonging to human leukocyte antigen (HLA) class I and class II DR molecules. It enables prediction of peptide binding to products of individual HLA alleles, combination of alleles, or HLA supertypes. NetMHCpan and NetMHCIIpan are used as prediction engines. The 13 HLA Class I supertypes are A1, A2, A3, A24, B7, B8, B27, B44, B58, B62, C1, and C4. The 13 HLA Class II DR supertypes are DR1, DR3, DR4, DR6, DR7, DR8, DR9, DR11, DR12, DR13, DR14, DR15, and DR16. In total, MULTIPRED2 enables prediction of peptide binding to 1077 variants representing 26 HLA supertypes. MULTIPRED2 has visualization modules for mapping promiscuous T-cell epitopes as well as those regions of high target concentration - referred to as T-cell epitope hotspots. Novel graphic representations are employed to display the predicted binding peptides and immunological hotspots in an intuitive manner and also to provide a global view of results as heat maps. Another function of MULTIPRED2, which has direct relevance to vaccine design, is the calculation of population coverage. Currently it calculates population coverage in five major groups in North America. MULTIPRED2 is an important tool to complement wet-lab experimental methods for identification of T-cell epitopes. It is available at http://cvc.dfci.harvard.edu/multipred2/.
AB - MULTIPRED2 is a computational system for facile prediction of peptide binding to multiple alleles belonging to human leukocyte antigen (HLA) class I and class II DR molecules. It enables prediction of peptide binding to products of individual HLA alleles, combination of alleles, or HLA supertypes. NetMHCpan and NetMHCIIpan are used as prediction engines. The 13 HLA Class I supertypes are A1, A2, A3, A24, B7, B8, B27, B44, B58, B62, C1, and C4. The 13 HLA Class II DR supertypes are DR1, DR3, DR4, DR6, DR7, DR8, DR9, DR11, DR12, DR13, DR14, DR15, and DR16. In total, MULTIPRED2 enables prediction of peptide binding to 1077 variants representing 26 HLA supertypes. MULTIPRED2 has visualization modules for mapping promiscuous T-cell epitopes as well as those regions of high target concentration - referred to as T-cell epitope hotspots. Novel graphic representations are employed to display the predicted binding peptides and immunological hotspots in an intuitive manner and also to provide a global view of results as heat maps. Another function of MULTIPRED2, which has direct relevance to vaccine design, is the calculation of population coverage. Currently it calculates population coverage in five major groups in North America. MULTIPRED2 is an important tool to complement wet-lab experimental methods for identification of T-cell epitopes. It is available at http://cvc.dfci.harvard.edu/multipred2/.
KW - HLA
KW - HLA supertype
KW - Human leukocyte antigen
KW - Promiscuous binding peptide
KW - T-cell epitope hotspots
KW - Vaccine design
UR - http://www.scopus.com/inward/record.url?scp=81255134467&partnerID=8YFLogxK
U2 - 10.1016/j.jim.2010.11.009
DO - 10.1016/j.jim.2010.11.009
M3 - Article
C2 - 21130094
AN - SCOPUS:81255134467
SN - 0022-1759
VL - 374
SP - 53
EP - 61
JO - Journal of Immunological Methods
JF - Journal of Immunological Methods
IS - 1-2
ER -