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Evaluation of the real-time protein adsorption kinetics on albumin-binding surfaces by dynamic in situ spectroscopic ellipsometry

机译:动态原位光谱椭偏仪评估白蛋白结合表面的实时蛋白质吸附动力学

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摘要

Functionalized surfaces with an affinity for albumin over competing serum proteins were prepared by immobilizing linear peptides or a small chemical ligand (SCL) with albumin-binding properties on silanized silicon surfaces. The real time adsorption of human serum albumin from single- and multi-component systems was monitored by dynamic ellipsometry. The experimentally obtained time-dependent adsorption data were analyzed by two models: a) a pseudo-first-order model and b) a biphasic kinetic model that accounted for the formation of tightly and loosely bound complexes. The biphasic kinetic model better fit the experimental data, and the binding constants were determined by non-linear regression analyses. The net forward rate constant for the tightly bound complex formation was distinctively higher for surfaces functionalized with peptides (~0.014 min~(-1)) when compared to surfaces functionalized with SCL (~10~(-1) min~(-1)).
机译:通过将线性蛋白或具有白蛋白结合特性的小化学配体(SCL)固定在硅烷化的硅表面上,可以制备对竞争血清蛋白具有白蛋白亲和力的功能化表面。通过动态椭偏仪监测单组分和多组分系统中人血清白蛋白的实时吸附。通过两种模型分析了实验获得的时间相关吸附数据:a)伪一级模型和b)解释了紧密结合和松散结合的复合物形成的双相动力学模型。双相动力学模型更好地拟合了实验数据,结合常数通过非线性回归分析确定。与用SCL功能化的表面(〜10〜(-1)min〜(-1)相比,用肽功能化的表面(〜0.014 min〜(-1))的紧密结合复合物形成的净前进速率常数明显更高。 )。

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