The Gram-positive bacterium causes severe disease globally. Vaccines that prevent infections induce antibodies against epitopes within the bacterial capsular polysaccharide (CPS). A better immunological understanding of the epitopes that protect from bacterial infection requires defined oligosaccharides obtained by total synthesis. The key to the synthesis of the serotype 12F CPS hexasaccharide repeating unit that is not contained in currently used glycoconjugate vaccines is the assembly of the trisaccharide β-D-GalNAc-(1→4)-[α-D-Glc-(1→3)]-β-D-ManNAcA, in which the branching points are equipped with orthogonal protecting groups. A linear approach relying on the sequential assembly of monosaccharide building blocks proved superior to a convergent [3 + 3] strategy that was not successful due to steric constraints. The synthetic hexasaccharide is the starting point for further immunological investigations.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301915 | PMC |
http://dx.doi.org/10.3762/bjoc.13.19 | DOI Listing |
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