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DIVERGENT CHEMOENZYMATIC SYNTHESIS OF SHIGELLA FLEXNERI PENTASACCHARIDES FOR VACCINE DEVELOPMENT

机译:Shigella Flexeri戊二糖的发散化学酶合成疫苗发育

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Enteroinvasive gram-negative bacteria from the Shigella flexneri (SF) species are of particular concern and a prime target for vaccine development [1]. Most SF serotypes exhibit closely related O-antigens (O-Ag) that are a main target of protection against reinfection. SF O-Ag backbones of interest comprise a unique repeating unit made of four residues (ABCD). Serotype specificity is determined by site-selective O-acetylation and α-D-glucosylation (E) (Fig. 1) [2]. The chemo-enzymatic conception of glycobricks, easy-to-assemble into biologically active molecules mimicking the O-Ag from various serotypes, is the keystone of an ongoing strategy to a synthetic carbohydrate-based Shigella vaccine
机译:来自Shigella Flexneri(SF)物种的肠化革兰阴性细菌特别关注和疫苗开发的主要目标[1]。大多数SF血清型都表现出密切相关的O-Antigens(O-AG),这是一种针对重生保护的主要目标。感兴趣的SF O-AG骨干包括由四个残基(ABCD)制成的独特重复单元。血清型特异性由位点选择性O-乙酰化和α-D-葡糖基化(E)(图1)[2]确定。糖蛋白的化学酶促酶促酶,易于组装成从各种血清型模仿O-AG的生物学上活性分子,是对基于合成的碳水化合物的志藻菌疫苗的持续策略的核心

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