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Synthetic Assembly of Mannose Moieties Using Polymer Chemistry and the Biological Evaluation of Its Interaction towards Concanavalin A

机译:高分子化学合成甘露糖部分及其与伴刀豆球蛋白A相互作用的生物学评估

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Protein–carbohydrate interactions exhibit myriad intracellular recognition events, so understanding and investigating their specific interaction with high selectivity and strength are of crucial importance. In order to examine the effect of multivalent binding on the specificity of protein–carbohydrate interactions, we synthesized mannose glycosides as a novel type of glycosylated monomer and glycopolymers of polyacrylamide derivatives with α-mannose (α-Man) by radical polymerization and monitored their strength of interaction with concanavalin A (Con A) by surface plasmon resonance (SPR) detection. In a quantitative test using the Con A-immobilized sensor surface, the kinetic affinity for the synthesized polymers, 8a (KD = 3.3 × 10?6 M) and 8b (KD = 5.3 × 10?5 M), were concentration-dependent, showing strong, specific molecular recognition abilities with lectin. Our study showed the enhancement in recognition specificity for multivalent saccharides, which is often mediated by cell surface carbohydrate-binding proteins that exhibit weak affinity and broad specificity for the individual ligands. View Full-Text
机译:蛋白质与碳水化合物的相互作用表现出无数的细胞内识别事件,因此以高选择性和高强度理解和研究它们的特异性相互作用至关重要。为了检验多价结合对蛋白质与碳水化合物相互作用特异性的影响,我们通过自由基聚合合成了甘露糖苷作为一种新型的糖基化单体和聚丙烯酰胺衍生物与α-甘露糖(α-Man)的糖聚合物,并监测了其强度表面等离振子共振(SPR)检测与伴刀豆球蛋白A(Con A)的相互作用在使用固定有Con A的传感器表面进行的定量测试中,合成聚合物8a(KD = 3.3×10?6 M)和8b(KD = 5.3×10?5 M)的动力学亲和力是浓度依赖性的,对凝集素具有很强的特异性分子识别能力。我们的研究表明,对多价糖类的识别特异性增强了,这通常是由细胞表面碳水化合物结合蛋白介导的,这些蛋白对单个配体表现出较弱的亲和力和广泛的特异性。查看全文

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