PAComplex: a web server to infer peptide antigen families and binding models from TCR–pMHC complexes

One of the most adaptive immune responses is triggered by specific T-cell receptors (TCR) binding to peptide-major histocompatibility complexes (pMHC). Despite the availability of many prediction servers to identify peptides binding to MHC, these servers are often lacking in peptide–TCR interactions and detailed atomic interacting models. PAComplex is the first web server investigating both pMHC and peptide-TCR interfaces to infer peptide antigens and homologous peptide antigens of a query. This server first identifies significantly similar TCR–pMHC templates (joint Z-value ≥ 4.0) of the query by using antibody–antigen and protein–protein interacting scoring matrices for peptide-TCR and pMHC interfaces, respectively. PAComplex then identifies the homologous peptide antigens of these hit templates from complete pathogen genome databases (≥108 peptide candidates from 864 628 protein sequences of 389 pathogens) and experimental peptide databases (80 057 peptides in 2287 species). Finally, the server outputs peptide antigens and homologous peptide antigens of the query and displays detailed interacting models (e.g. hydrogen bonds and steric interactions in two interfaces) of hitTCR-pMHC templates. Experimental results demonstrate that the proposed server can achieve high prediction accuracy and offer potential peptide antigens across pathogens. We believe that the server is able to provide valuable insights for the peptide vaccine and MHC restriction. The PAComplex sever is available at http://PAcomplex.life.nctu.edu.tw.

[1]  M. Miyata Unique centipede mechanism of Mycoplasma gliding. , 2010, Annual review of microbiology.

[2]  Ding‐Shinn Chen,et al.  Hepatitis B Virus Infection , 2007 .

[3]  A Sette,et al.  A structure-based algorithm to predict potential binding peptides to MHC molecules with hydrophobic binding pockets. , 1997, Human immunology.

[4]  Alessandro Sette,et al.  The Immune Epitope Database 2.0 , 2009, Nucleic Acids Res..

[5]  Oliver Kohlbacher,et al.  SVMHC: a server for prediction of MHC-binding peptides , 2006, Nucleic Acids Res..

[6]  R. Bartenschlager,et al.  The amino‐terminal domain of the hepadnaviral P‐gene encodes the terminal protein (genome‐linked protein) believed to prime reverse transcription. , 1988, The EMBO journal.

[7]  F. Sinigaglia,et al.  Promiscuous and allele-specific anchors in HLA-DR-binding peptides , 1993, Cell.

[8]  Gajendra P. S. Raghava,et al.  MHCBN: a comprehensive database of MHC binding and non-binding peptides , 2003, Bioinform..

[9]  G. Crooks,et al.  WebLogo: a sequence logo generator. , 2004, Genome research.

[10]  A. Rudensky,et al.  Sequence analysis of peptides bound to MHC class II molecules , 1991, Nature.

[11]  Jinn-Moon Yang,et al.  3D-partner: a web server to infer interacting partners and binding models , 2007, Nucleic Acids Res..

[12]  R. Bartenschlager,et al.  Hepadnaviral assembly is initiated by polymerase binding to the encapsidation signal in the viral RNA genome. , 1992, The EMBO journal.

[13]  Alessandro Sette,et al.  Generating quantitative models describing the sequence specificity of biological processes with the stabilized matrix method , 2005, BMC Bioinformatics.

[14]  Ian A Wilson,et al.  The specificity of TCR/pMHC interaction. , 2002, Current opinion in immunology.

[15]  P. Kloetzel,et al.  MAPPP: MHC class I antigenic peptide processing prediction. , 2003, Applied bioinformatics.

[16]  C. Thio,et al.  Review of hepatitis B therapeutics. , 2010, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[17]  Ian A Wilson,et al.  Structural and thermodynamic correlates of T cell signaling. , 2002, Annual review of biophysics and biomolecular structure.

[18]  Y. Sykulev,et al.  How a T Cell Receptor-like Antibody Recognizes Major Histocompatibility Complex-bound Peptide* , 2008, Journal of Biological Chemistry.

[19]  Mathias M Schuler,et al.  SYFPEITHI: database for searching and T-cell epitope prediction. , 2007, Methods in molecular biology.

[20]  A. Giuliani,et al.  A computational approach identifies two regions of Hepatitis C Virus E1 protein as interacting domains involved in viral fusion process , 2009, BMC Structural Biology.

[21]  Vladimir Brusic,et al.  MHCPEP, a database of MHC-binding peptides: update 1996 , 1997, Nucleic Acids Res..

[22]  Philippa Marrack,et al.  Evolutionarily conserved amino acids that control TCR-MHC interaction. , 2008, Annual review of immunology.

[23]  Baris E. Suzek,et al.  The Universal Protein Resource (UniProt) in 2010 , 2009, Nucleic Acids Res..

[24]  Ettore Appella,et al.  Single MHC mutation eliminates enthalpy associated with T cell receptor binding. , 2007, Journal of molecular biology.

[25]  W. M. Lee,et al.  Hepatitis B virus infection. , 1997, The New England journal of medicine.

[26]  Debasisa Mohanty,et al.  MODPROPEP: a program for knowledge-based modeling of protein–peptide complexes , 2007, Nucleic Acids Res..