Antibody Recognition of Cancer-Related Gangliosides and Their Mimics Investigated Using in silico Site Mapping

被引:14
作者
Agostino, Mark [1 ]
Yuriev, Elizabeth [1 ]
Ramsland, Paul A. [2 ,3 ,4 ]
机构
[1] Monash Univ, Monash Inst Pharmaceut Sci, Parkville, Vic, Australia
[2] Burnet Inst, Ctr Immunol, Melbourne, Vic, Australia
[3] Univ Melbourne, Dept Surg Austin Hlth, Heidelberg, Vic, Australia
[4] Monash Univ, Dept Immunol, Melbourne, Vic 3004, Australia
来源
PLOS ONE | 2012年 / 7卷 / 04期
关键词
GUILLAIN-BARRE-SYNDROME; GD2; GANGLIOSIDE; MONOCLONAL-ANTIBODY; PEPTIDES MIMICKING; ANTIGANGLIOSIDE ANTIBODIES; XENOREACTIVE ANTIBODIES; CARBOHYDRATE ANTIGENS; CANONICAL STRUCTURES; MOLECULAR MIMICRY; LIGAND DOCKING;
D O I
10.1371/journal.pone.0035457
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Modified gangliosides may be overexpressed in certain types of cancer, thus, they are considered a valuable target in cancer immunotherapy. Structural knowledge of their interaction with antibodies is currently limited, due to the large size and high flexibility of these ligands. In this study, we apply our previously developed site mapping technique to investigate the recognition of cancer-related gangliosides by anti-ganglioside antibodies. The results reveal a potential ganglioside-binding motif in the four antibodies studied, suggesting the possibility of structural convergence in the anti-ganglioside immune response. The structural basis of the recognition of ganglioside-mimetic peptides is also investigated using site mapping and compared to ganglioside recognition. The peptides are shown to act as structural mimics of gangliosides by interacting with many of the same binding site residues as the cognate carbohydrate epitopes. These studies provide important clues as to the structural basis of immunological mimicry of carbohydrates.
引用
收藏
页数:12
相关论文
共 67 条
[1]  
Agostino M., 2012, ANTICARBOHYDRATE ANT, P203, DOI [10.1007/978-3-7091-0870-3_9, DOI 10.1007/978-3-7091-0870-3_9]
[2]   A computational approach for exploring carbohydrate recognition by lectins in innate immunity [J].
Agostino, Mark ;
Yuriev, Elizabeth ;
Ramsland, Paul A. .
FRONTIERS IN IMMUNOLOGY, 2011, 2
[3]   Carbohydrate-mimetic peptides: structural aspects of mimicry and therapeutic implications [J].
Agostino, Mark ;
Sandrin, Mauro S. ;
Thompson, Philip E. ;
Farrugia, William ;
Ramsland, Paul A. ;
Yuriev, Elizabeth .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2011, 11 (02) :211-224
[4]   Peptide Inhibitors of Xenoreactive Antibodies Mimic the Interaction Profile of the Native Carbohydrate Antigens [J].
Agostino, Mark ;
Sandrin, Mauro S. ;
Thompson, Philip E. ;
Ramsland, Paul A. ;
Yuriev, Elizabeth .
BIOPOLYMERS, 2011, 96 (02) :193-206
[5]   Identification of preferred carbohydrate binding modes in xenoreactive antibodies by combining conformational filters and binding site maps [J].
Agostino, Mark ;
Sandrin, Mauro S. ;
Thompson, Philip E. ;
Yuriev, Elizabeth ;
Ramsland, Paul A. .
GLYCOBIOLOGY, 2010, 20 (06) :724-735
[6]   In silico analysis of antibody-carbohydrate interactions and its application to xenoreactive antibodies [J].
Agostino, Mark ;
Sandrin, Mauro S. ;
Thompson, Philip E. ;
Yuriev, Elizabeth ;
Ramsland, Paul A. .
MOLECULAR IMMUNOLOGY, 2009, 47 (2-3) :233-246
[7]   Molecular Docking of Carbohydrate Ligands to Antibodies: Structural Validation against Crystal Structures [J].
Agostino, Mark ;
Jene, Cassandra ;
Boyle, Tristan ;
Ramsland, Paul A. ;
Yuriev, Elizabeth .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2009, 49 (12) :2749-2760
[8]   Standard conformations for the canonical structures of immunoglobulins [J].
AlLazikani, B ;
Lesk, AM ;
Chothia, C .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 273 (04) :927-948
[9]  
[Anonymous], PRIM VERS 2 2
[10]  
[Anonymous], 2010, The PyMOL Molecular Graphics System (2.5.4)