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Analysis of Density-Dependent Binding of Glycans by Lectins Using Carbohydrate Microarrays

机译:使用碳水化合物微阵列分析凝集素对聚糖的密度依赖性结合

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摘要

To investigate the density-dependent binding of glycans by lectins using carbohydrate microarrays, a number of C-terminal hydrazide-conjugated neoglycopeptides with various valences and different spatial arrangements of the sugar ligands were prepared on a solid support. The synthetic strategy includes (1) assembly of alkyne-linked peptides possessing C-terminal hydrazide on a solid support, (2) coupling of azide-linked, unprotected sugars to the alkyne-linked peptides on the solid support utilizing click chemistry, and (3) release of the neo-glycopeptides from the solid support. By using this synthetic methodology, sixty five neoglycopeptides with a valency ranging from 1 to 4 and different spatial arrangements of the carbohydrate ligands were generated. Carbohydrate microarrays were constructed by immobilizing the prepared neoglycopeptides on epoxide-derivatized glass slides and were used to analyze the density-dependent binding of glycans by lectins. The results of binding property determinations show that lectin binding is highly dependent on the surface glycan density.
机译:为了研究使用碳水化合物微阵列的凝集素对聚糖的密度依赖性结合,在固体支持物上制备了具有不同化合价和糖配体的不同空间排列的许多C末端酰肼偶联的新糖肽。合成策略包括(1)在固体支持物上组装具有C-末端酰肼的炔烃连接肽,(2)利用点击化学将叠氮化物连接的未保护糖与固体支持物上的炔烃连接肽偶联,和( 3)从固体支持物中释放新糖肽。通过使用这种合成方法,生成了六价的新糖肽,化合价为1-4,碳水化合物配体的空间排列不同。通过将制备的新糖肽固定在环氧衍生化的载玻片上来构建碳水化合物微阵列,并将其用于分析凝集素对聚糖的密度依赖性结合。结合性质测定的结果表明,凝集素结合高度依赖于表面聚糖密度。

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