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Polyoxazolines with a Vicinally Double-Bioactivated Terminus for Biomacromolecular Affinity Assessment

机译:具有邻近双生物激活末端的聚恶唑啉,用于生物分子亲和力评估

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摘要

Interactions between proteins and carbohydrates with larger biomacromolecules, e.g., lectins, are usually examined using self-assembled monolayers on target gold surfaces as a simplified model measuring setup. However, most of those measuring setups are either limited to a single substrate or do not allow for control over ligand distance and spacing. Here, we develop a synthetic strategy, consisting of a cascade of a thioesterification, native chemical ligation (NCL) and thiol-ene reaction, in order to create three-component polymer conjugates with a defined double bioactivation at the chain end. The target architecture is the vicinal attachment of two biomolecule residues to the α telechelic end point of a polymer and a thioether group at the ω chain end for fixating the conjugate to a gold sensor chip surface. As proof-of-principle studies for affinity measurements, we demonstrate the interaction between covalently bound mannose and ConA in surface acoustic wave (SAW) and surface plasmon resonance (SPR) experiments.
机译:通常使用在靶金表面上的自组装单层作为简化的模型测量设置,在蛋白质和碳水化合物之间的相互作用,例如凝集素,例如凝集素。然而,大多数测量设置都限于单个基板,或者不允许控制配体距离和间隔。在这里,我们开发一种合成策略,由甲腈化,天然化学连接(NCl)和硫醇 - 烯反应组成,以产生三分组分聚合物缀合物,以在链末端具有定义的双重生物活化。目标结构是两种生物分子残基的静脉连接到聚合物的α焦点终点和ω链端的硫醚基团,用于将缀合物固定到金传感器芯片表面上。作为亲和力测量的原则上研究,我们证明了在表面声波(SAW)和表面等离子体共振(SPR)实验中的共价结合的甘露糖和Cona之间的相互作用。

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