Seeberger Peter H, Pereira Claney L, Govindan Subramanian
Department of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476 Potsdam, Germany; Department of Chemistry and Biochemistry, Freie Universität Berlin, Arnimallee 22, 14195 Berlin, Germany.
Vaxxilon Deutschland GmbH, Magnusstrasse 11, 12489 Berlin, Germany.
Beilstein J Org Chem. 2017 Jan 25;13:164-173. doi: 10.3762/bjoc.13.19. eCollection 2017.
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.
这种革兰氏阳性细菌在全球范围内引发严重疾病。预防感染的疫苗可诱导产生针对细菌荚膜多糖(CPS)内表位的抗体。要更好地从免疫学角度理解能预防细菌感染的表位,需要通过全合成获得特定的寡糖。合成目前使用的糖缀合物疫苗中不含有的血清型12F CPS六糖重复单元的关键在于三糖β-D-氨基半乳糖-(1→4)-[α-D-葡萄糖-(1→3)]-β-D-甘露糖醛酸的组装,其中分支点带有正交保护基团。事实证明,依靠单糖构建单元的顺序组装的线性方法优于收敛性的[3 + 3]策略,后者因空间位阻而未成功。合成的六糖是进一步免疫学研究的起点。