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PolysacDB ID | 1070 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | The capsular polysaccharide, also known as K-antigen consists of repeating units of following residues : -8)α-Neup5Ac(2- [a homopolymer of α(2-->8) sialic acid residues] |
BCSDB Structure | 139710 |
Proposed functions | N/A |
Antigenic Nature used to produce antibodies | Live group B type 15 meningococci cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab 2-2-B |
Antibody type and class | IgM |
Assay System | ELISA and Radioimmunoassay |
Cross-reactivity | This antibody cross-reacted with E. coli strain K1 Capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab provided protection against the E. coli K-1 strain |
Curator ID | AA + AS |
Date of Curation | 21-01-2010 |
References | PMC261141 |
PolysacDB ID | 1578 |
Carbohydrate Name | N-propionylated group B meningococcal polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | Nil |
Antibodies | Polysera |
Antibody type and class | N/A |
Assay System | Radioactive binding inhibition assay, ELISA, Bactericidal assay |
Cross-reactivity | This antisera cross-reacted with capsular polysaccharide of E. coli K1 |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This antisera was bactericidal for Group B meningococci |
Curator ID | AA + AS |
Date of Curation | 12-09-2010 |
References | 2469720 |
PolysacDB ID | 1579 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 10 |
Antibody type and class | IgG1 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 13-09-2010 |
References | 9590252 |
PolysacDB ID | 1580 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 11 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide. This Mab also cross-reacted with polysialic acid on CHP-134 neuroblastoma cells |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit complement |
Curator ID | AA + AS |
Date of Curation | 13-09-2010 |
References | 9590252 |
PolysacDB ID | 1581 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 12 |
Antibody type and class | IgG2a |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide. This Mab also cross-reacted with polysialic acid on CHP-134 neuroblastoma cells |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit and human complement |
Curator ID | AA + AS |
Date of Curation | 13-09-2010 |
References | 9590252 |
PolysacDB ID | 1582 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 13 |
Antibody type and class | IgG3 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide. This Mab also cross-reacted with polysialic acid on CHP-134 neuroblastoma cells |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit and human complement |
Curator ID | AA + AS |
Date of Curation | 14-09-2010 |
References | 9590252 |
PolysacDB ID | 1583 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 14 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide. This Mab also cross-reacted with polysialic acid on CHP-134 neuroblastoma cells |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit complement |
Curator ID | AA + AS |
Date of Curation | 14-09-2010 |
References | 9590252 |
PolysacDB ID | 1584 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 15 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide. This Mab also cross-reacted with polysialic acid on CHP-134 neuroblastoma cells |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit complement |
Curator ID | AA + AS |
Date of Curation | 14-09-2010 |
References | 9590252 |
PolysacDB ID | 1585 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 16 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit complement |
Curator ID | AA + AS |
Date of Curation | 15-09-2010 |
References | 9590252 |
PolysacDB ID | 1586 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 17 |
Antibody type and class | IgM |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 16-09-2010 |
References | 9590252 |
PolysacDB ID | 1587 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 18 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide. This Mab also cross-reacted with polysialic acid on CHP-134 neuroblastoma cells |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit and human complement |
Curator ID | AA + AS |
Date of Curation | 16-09-2010 |
References | 9590252 |
PolysacDB ID | 1588 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 19 |
Antibody type and class | IgG2a |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 16-09-2010 |
References | 9590252 |
PolysacDB ID | 1589 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 20 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 16-09-2010 |
References | 9590252 |
PolysacDB ID | 1590 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 21 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 16-09-2010 |
References | 9590252 |
PolysacDB ID | 1591 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 22 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 17-09-2010 |
References | 9590252 |
PolysacDB ID | 1592 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 23 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 17-09-2010 |
References | 9590252 |
PolysacDB ID | 1593 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 24 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 17-09-2010 |
References | 9590252 |
PolysacDB ID | 1594 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 25 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 17-09-2010 |
References | 9590252 |
PolysacDB ID | 1595 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 26 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide. This Mab also cross-reacted with polysialic acid on CHP-134 neuroblastoma cells |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit complement |
Curator ID | AA + AS |
Date of Curation | 18-09-2010 |
References | 9590252 |
PolysacDB ID | 1596 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 28 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide. This Mab also cross-reacted with polysialic acid on CHP-134 neuroblastoma cells |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit complement |
Curator ID | AA + AS |
Date of Curation | 18-09-2010 |
References | 9590252 |
PolysacDB ID | 1597 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 29 |
Antibody type and class | IgG2a |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide. This Mab also cross-reacted with polysialic acid on CHP-134 neuroblastoma cells |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 18-09-2010 |
References | 9590252 |
PolysacDB ID | 1598 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 30 |
Antibody type and class | IgG3 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide. This Mab also cross-reacted with polysialic acid on CHP-134 neuroblastoma cells |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit and human complement |
Curator ID | AA + AS |
Date of Curation | 19-09-2010 |
References | 9590252 |
PolysacDB ID | 1599 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 48 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit complement |
Curator ID | AA + AS |
Date of Curation | 19-09-2010 |
References | 9590252 |
PolysacDB ID | 1600 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 2 |
Antibody type and class | IgG3 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit and human complement |
Curator ID | AA + AS |
Date of Curation | 20-09-2010 |
References | 9590252 |
PolysacDB ID | 1601 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 6 |
Antibody type and class | IgG3 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 20-09-2010 |
References | 9590252 |
PolysacDB ID | 1602 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 9 |
Antibody type and class | IgG1 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 20-09-2010 |
References | 9590252 |
PolysacDB ID | 1603 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 1 |
Antibody type and class | IgG3 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit complement |
Curator ID | AA + AS |
Date of Curation | 20-09-2010 |
References | 9590252 |
PolysacDB ID | 1604 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 35 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab cross-reacted with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 21-09-2010 |
References | 9590252 |
PolysacDB ID | 1605 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 3 |
Antibody type and class | IgG2b |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit complement |
Curator ID | AA + AS |
Date of Curation | 21-09-2010 |
References | 9590252 |
PolysacDB ID | 1606 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 4 |
Antibody type and class | IgG1 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease |
Curator ID | AA + AS |
Date of Curation | 22-09-2010 |
References | 9590252 |
PolysacDB ID | 1607 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 5 |
Antibody type and class | IgG3 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit and human complement |
Curator ID | AA + AS |
Date of Curation | 22-09-2010 |
References | 9590252 |
PolysacDB ID | 1608 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 7 |
Antibody type and class | IgG3 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit and human complement |
Curator ID | AA + AS |
Date of Curation | 22-09-2010 |
References | 9590252 |
PolysacDB ID | 1609 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Glycoconjugates |
Carrier Name | Tetanus toxoid |
Conjugation Method | The oligosaccharide-protein conjugate was prepared by stirring a mixture of terminal aldehyde-containing N-Pr meningococcal B oligosaccharide with tetanus toxoid in 0.75 M potassium phosphate buffer, pH 9.0, with sodium cyanoborohydride (40 mg/ml) for 1 day at 40°C, then 2 days at ambient temperature |
Antibodies | Mab Seam 8 |
Antibody type and class | IgG3 |
Assay System | ELISA, flow cytometry and indirect immunofluorescence |
Cross-reactivity | This Mab did not cross-react with non-modified acetylaed group B capsular polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab may be useful for the identification of molecular mimetics capable of eliciting protective antibodies specific to the bacteria, without the risk of evoking autoimmune disease. This Mab induced bactericidal activity with rabbit and human complement |
Curator ID | AA + AS |
Date of Curation | 22-09-2010 |
References | 9590252 |
PolysacDB ID | 1610 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | A patient suffering from IgM lambda monoclonal gammopathy |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab NOV |
Antibody type and class | IgM |
Assay System | Ouchterlony Gel Diffusion, ELISA, invivo protection assays |
Cross-reactivity | This Mab reacted with group B meningococcal and E. coli K1 capsular polysaccharides and did not react with a(2 --> 9)-linked poly-N-acetylneuraminic acid, the capsular polysaccharide of the group C meningococcus, nor with the capsular polysaccharide of E. coli K92 or K100. It also crossreacts with polynucleotides and denatured DNA |
Proposed epitopes | The epitope was proposed to consist of α(2-->8)-linked poly-N-acetylneuraminic acid |
IEDB Epitope | N/A |
Proposed Utility | This Mab is protective against E. coli in newborn rats |
Curator ID | AA + AS |
Date of Curation | 22-09-2010 |
References | PMC2188242 |
PolysacDB ID | 1611 |
Carbohydrate Name | N-propionyl substituted Neisseria meningitidis group B capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It is a homopolymer of α(2-->8) sialic acid |
BCSDB Structure | N/A |
Proposed functions | This capsular polysaccharide is an important virulence determinant. Serum antibodies to the group B polysaccharide confers protection against disease by activating complement-mediated bacteriolysis and/or opsonization. It leads to immunologic tolerance induced by prenatal exposure to host polysialyated glycoproteins |
Antigenic Nature used to produce antibodies | Whole cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab 735D4 |
Antibody type and class | IgG2a |
Assay System | ELISA, Immunoelectrophoresis and immunodiffusion |
Cross-reactivity | This Mab reacted with with all E. coli K1 and group B meningococcal strains tested but did not react with E. coli strains having capsular types K12, K13, K14, and K92; and group A and C meningococci |
Proposed epitopes | The epitope was proposed to consist of repeating α(2-->8)-linked Neu5Ac units |
IEDB Epitope | N/A |
Proposed Utility | This antibody is an important addition to the analyticaln tools available for the study of the structure and function of the E. coli K1 and meningococcal B capsules |
Curator ID | AA + AS |
Date of Curation | 22-09-2010 |
References | 397221 |
PolysacDB ID | 1802 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Whole cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab 2-2-B |
Antibody type and class | IgM |
Assay System | ELISA |
Cross-reactivity | This Mab was specific to Serogroup B and did not cross-react with other serogroups |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab would help in serogrouping of Neisseria meningitidis strains |
Curator ID | AA + AS |
Date of Curation | 04-11-2010 |
References | PMC540207 |
PolysacDB ID | 1806 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Whole cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab 101C11 |
Antibody type and class | IgG2a |
Assay System | ELISA and bactericidal assays |
Cross-reactivity | This Mab was specifc to Neisseria meningitidis group B and did not cross-react with group A and group C N. meningitidis capsular polysaccharides. This Mab also recognized N-propionylated capsular polysaccharide of group B meningitidis |
Proposed epitopes | α[2-->8] linked N-acetyl neuraminic acid residues seemed to be the part of the epitope |
IEDB Epitope | N/A |
Proposed Utility | This Mab had potent bactericidal activity |
Curator ID | AA + AS |
Date of Curation | 05-11-2010 |
References | 1284118 |
PolysacDB ID | 1807 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Whole cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab 30H12 |
Antibody type and class | IgG2a |
Assay System | ELISA and bactericidal assays |
Cross-reactivity | This Mab was specifc to Neisseria meningitidis group B and did not cross-react with group A and group C N. meningitidis capsular polysaccharides. This Mab did not recognized N-propionylated capsular polysaccharide of group B meningitidis |
Proposed epitopes | α[2-->8] linked N-acetyl neuraminic acid residues seemed to be the part of the epitope |
IEDB Epitope | N/A |
Proposed Utility | This Mab had potent bactericidal activity |
Curator ID | AA + AS |
Date of Curation | 05-11-2010 |
References | 1284118 |
PolysacDB ID | 1862 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Whole cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab 10C11 |
Antibody type and class | IgG2a |
Assay System | ELISA and bactericidal assays |
Cross-reactivity | This Mab cross-reacts with E. coli K1 polysaccharide but does not react with E. coli K92, group A and group C polysaccharides of Neisseria meningitidis. This Mab also reacts with N-propionylated group B polysaccharide |
Proposed epitopes | The epitope consisted of α2-8 linked sialic acid residues |
IEDB Epitope | N/A |
Proposed Utility | This Mab had bactericidal activity |
Curator ID | AA + AS |
Date of Curation | 18-11-2010 |
References | 1284118 |
PolysacDB ID | 1864 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Infected patient |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab BES |
Antibody type and class | IgM |
Assay System | ELISA, Rat protection assay |
Cross-reactivity | This Mab cross-reacts with E. coli K1 polysaccharide but does not react with E. coli K92, group A and group C polysaccharides of Neisseria meningitidis. This Mab also reacts with N-propionylated group B polysaccharide |
Proposed epitopes | The epitope consisted of α2-8 linked N-acetylneuraminic acid acid residues |
IEDB Epitope | N/A |
Proposed Utility | This antibody protected infant rats from bacteremia caused by Escherichia coli K1 |
Curator ID | AA + AS |
Date of Curation | 18-11-2010 |
References | PMC173242 |
PolysacDB ID | 1865 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Infected patient |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab KLOT |
Antibody type and class | IgM |
Assay System | ELISA, Rat protection assay |
Cross-reactivity | This Mab cross-reacts with E. coli K1 polysaccharide but does not react with E. coli K92, group A and group C polysaccharides of Neisseria meningitidis. This Mab also reacts with N-propionylated group B polysaccharide |
Proposed epitopes | The epitope consisted of α2-8 linked N-acetylneuraminic acid acid residues |
IEDB Epitope | N/A |
Proposed Utility | This antibody protected infant rats from bacteremia caused by Escherichia coli K1 |
Curator ID | AA + AS |
Date of Curation | 18-11-2010 |
References | PMC173242 |
PolysacDB ID | 1866 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Infected patient |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab LOG |
Antibody type and class | IgM |
Assay System | ELISA, Rat protection assay |
Cross-reactivity | This Mab cross-reacts with E. coli K1 polysaccharide but does not react with E. coli K92, group A and group C polysaccharides of Neisseria meningitidis. This Mab also reacts with N-propionylated group B polysaccharide |
Proposed epitopes | The epitope consisted of α2-8 linked N-acetylneuraminic acid acid residues |
IEDB Epitope | N/A |
Proposed Utility | This antibody protected infant rats from bacteremia caused by Escherichia coli K1 |
Curator ID | AA + AS |
Date of Curation | 18-11-2010 |
References | PMC173242 |
PolysacDB ID | 1867 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Infected patient |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab VAN |
Antibody type and class | IgM |
Assay System | ELISA, Rat protection assay |
Cross-reactivity | This Mab cross-reacts with E. coli K1 polysaccharide but does not react with E. coli K92, group A and group C polysaccharides of Neisseria meningitidis. This Mab also reacts with N-propionylated group B polysaccharide |
Proposed epitopes | The epitope consisted of α2-8 linked N-acetylneuraminic acid acid residues |
IEDB Epitope | N/A |
Proposed Utility | This antibody protected infant rats from bacteremia caused by Escherichia coli K1 |
Curator ID | AA + AS |
Date of Curation | 18-11-2010 |
References | PMC173242 |
PolysacDB ID | 1868 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Infected patient |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab HUFF |
Antibody type and class | IgM |
Assay System | ELISA, Rat protection assay |
Cross-reactivity | This Mab cross-reacts with E. coli K1 polysaccharide but does not react with E. coli K92, group A and group C polysaccharides of Neisseria meningitidis. This Mab also reacts with N-propionylated group B polysaccharide |
Proposed epitopes | The epitope consisted of α2-8 linked N-acetylneuraminic acid acid residues |
IEDB Epitope | N/A |
Proposed Utility | This antibody protected infant rats from bacteremia caused by Escherichia coli K1 |
Curator ID | AA + AS |
Date of Curation | 18-11-2010 |
References | PMC173242 |
PolysacDB ID | 1869 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Infected patient |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab LIP |
Antibody type and class | IgM |
Assay System | ELISA, Rat protection assay |
Cross-reactivity | This Mab cross-reacts with E. coli K1 polysaccharide but does not react with E. coli K92, group A and group C polysaccharides of Neisseria meningitidis. This Mab also reacts with N-propionylated group B polysaccharide |
Proposed epitopes | The epitope consisted of α2-8 linked N-acetylneuraminic acid acid residues |
IEDB Epitope | N/A |
Proposed Utility | This antibody protected infant rats from bacteremia caused by Escherichia coli K1 |
Curator ID | AA + AS |
Date of Curation | 19-11-2010 |
References | PMC173242 |
PolysacDB ID | 1870 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Infected patient |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab SLAD |
Antibody type and class | IgM |
Assay System | ELISA, Rat protection assay |
Cross-reactivity | This Mab cross-reacts with E. coli K1 polysaccharide but does not react with E. coli K92, group A and group C polysaccharides of Neisseria meningitidis. This Mab also reacts with N-propionylated group B polysaccharide |
Proposed epitopes | The epitope consisted of α2-8 linked N-acetylneuraminic acid acid residues |
IEDB Epitope | N/A |
Proposed Utility | This antibody protected infant rats from bacteremia caused by Escherichia coli K1 |
Curator ID | AA + AS |
Date of Curation | 19-11-2010 |
References | PMC173242 |
PolysacDB ID | 1871 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Tonsillar B cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab 5E1 |
Antibody type and class | IgM |
Assay System | ELISA |
Cross-reactivity | This Mab reacts with E. coli K1 polysaccharide |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This antibody protected infant rats from bacteremia caused by Escherichia coli K1 |
Curator ID | AA + AS |
Date of Curation | 19-11-2010 |
References | 1988519 |
PolysacDB ID | 1889 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Whole cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab MB22 |
Antibody type and class | IgM |
Assay System | Counter immunoelectrophoresis and slide agglutination tests |
Cross-reactivity | This Mab was specific to group B polysaccharide and did not cross-react with Haemophilus influenza and Streptococcus pneumoniae. This Mab also cross-reacted with N. meningitidis group C polysaccharide antigen, an alpha (2->9)-linked homopolymer of sialic acid residues |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab can be used in culture identification. |
Curator ID | AA + AS |
Date of Curation | 23-11-2010 |
References | PMC269298 |
PolysacDB ID | 1890 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Whole cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab 36 |
Antibody type and class | IgM |
Assay System | Counter immunoelectrophoresis and slide agglutination tests |
Cross-reactivity | This Mab was specific to group B polysaccharide and did not cross-react with Haemophilus influenza and Streptococcus pneumoniae |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab can be used in culture identification. |
Curator ID | AA + AS |
Date of Curation | 23-11-2010 |
References | PMC269298 |
PolysacDB ID | 1891 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Whole cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab 62 |
Antibody type and class | IgM |
Assay System | Counter immunoelectrophoresis and slide agglutination tests |
Cross-reactivity | This Mab was specific to group B polysaccharide and did not cross-react with Haemophilus influenza and Streptococcus pneumoniae |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab can be used in culture identification. |
Curator ID | AA + AS |
Date of Curation | 23-11-2010 |
References | PMC269298 |
PolysacDB ID | 1892 |
Carbohydrate Name | Capsular polysaccharide (Drugpedia) |
Carbohydrate Class | Capsular polysaccharide |
Microbe | Neisseria meningitidis Serogroup B (NCBI Taxonomy) (Drugpedia) |
Basic Structure | It consists of a homopolymer of α(2-->8)-linked sialic acid residues |
BCSDB Structure | 7487 |
Proposed functions | It is an important virulence factor |
Antigenic Nature used to produce antibodies | Whole cells |
Carrier Name | Nil |
Conjugation Method | Nil |
Antibodies | Mab 85 |
Antibody type and class | IgM |
Assay System | Counter immunoelectrophoresis and slide agglutination tests |
Cross-reactivity | This Mab was specific to group B polysaccharide and did not cross-react with Haemophilus influenza and Streptococcus pneumoniae |
Proposed epitopes | N/A |
IEDB Epitope | N/A |
Proposed Utility | This Mab can be used in culture identification. |
Curator ID | AA + AS |
Date of Curation | 23-11-2010 |
References | PMC269298 |
Bioinformatics Centre, Institute of Microbial Technology, Sec - 39A, Chandigarh, India - 160036 |