Alternative title | Helical epitope of the group B meningococcal alpha(2-8)-linked sialic acid polysaccharide |
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Download | - View final version: Helical epitope of the group B meningococcal α(2-8)-linked sialic acid polysaccharide (PDF, 1.2 MiB)
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DOI | Resolve DOI: https://doi.org/10.1021/bi00136a012 |
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Author | Search for: Brisson, Jean-Robert1; Search for: Baumann, Herbert1; Search for: Imberty, Anne; Search for: Pérez, Serge; Search for: Jennings, Harold J.1 |
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Affiliation | - National Research Council of Canada. NRC Institute for Biological Sciences
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Format | Text, Article |
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Subject | acid; acids; alpha; antibodies; antibody; antigen; antigens; antigens,bacterial; bacterial; binding; calculation; calculations; Canada; carbohydrate conformation; carbohydrate sequence; chemistry; coil; conformation; conformational; constraints; difference; distribution; energy; energy calculations; enhancement; epitope; epitopes; group-B; helices; helix; immunology; magnetic resonance spectroscopy; model; molecular sequence data; monoclonal-antibodies; monoclonal-antibody; NMR; nuclear; oligosaccharide; Overhauser; Overhauser enhancement; parameters; polysaccharide; polysaccharides; polysaccharides,bacterial; potential; recognition; sialic; sialic acids; sialic-acid; solution; trisaccharide |
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Abstract | The immunological properties of the group B meningococcal α(2-8)-linked sialic acid polysaccharide have been rationalized in terms of a model where the random coil nature of the polymer can be described by the presence of local helices. The conformational versatility of the α NeuAc(2-8)α NeuAc linkage has been explored by NMR studies at 600 MHz in conjunction with potential energy calculations for colominic acid, an α(2-8)NeuAc polymer, and the trisaccharide α NeuAc(2-8)α NeuAc(2-8)β NeuAc. Potential energy calculations were used to estimate the energetically favorable conformers and to describe the wide range of helices which the polymer can adopt. No unique conformer was found to satisfy all NMR constraints, and only ensemble averaged nuclear Overhauser enhancements could correctly simulate the experimental data. Conformational differences between the polymer and the trisaccharide could be best explained in terms of slight changes in the relative distribution of conformers in solution. Similar helical parameters for the α(2-8)NeuAc polymer and poly(A) were proposed as the basis for their cross-reactivity to a monoclonal antibody IgMNOV. The unusual length dependency for binding of oligosaccharide to group B specific antibodies was postulated to arise from the recognition of a high-order local helix with an extended conformation which was not highly populated in solution |
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Publication date | 1992-06-02 |
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Publisher | American Chemical Society |
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In | |
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Language | English |
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Peer reviewed | Yes |
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Identifier | NRC-IBS-BRISSON1992 |
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NRC number | NRCC-32011 |
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NPARC number | 9363400 |
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Export citation | Export as RIS |
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Report a correction | Report a correction (opens in a new tab) |
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Record identifier | 88a42b18-d5ea-4595-898c-93f9b254c4cd |
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Record created | 2009-07-10 |
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Record modified | 2020-05-27 |
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