蛋白质的界面吸附及其生物活性因它在构建生物传感、生物电子器件和生物燃料电池等方面具有重要的作用而倍受关注.对此,界面电场是吸附的一个重要影响因素,它能明显地影响蛋白质分子在材料界面的吸附量、分子构象以及分子定向.本文应用电化学方法和红外光谱技术研究了血红蛋白在三维多孔金膜电极上的吸附动力学及其生物活性随界面电场的变化关系.结果表明,由界面电场产生的过量表面电荷可借助与蛋白质分子之间的静电作用加速蛋白质分子在电极表面的吸附,提高其吸附量;但是,过高的界面电场将破坏吸附蛋白质的构象以及降低它还原过氧化氢的催化活性;只有在零电荷电位下,吸附在电极表面的血红蛋白才能保持其天然的构象和生物催化活性.本研究将为生物传感器、生物电子器件和生物燃料电池的构建提供理论依据,加深对荷电生物界面上生物分子界面行为的认识.
The adsorption and bioactivity of proteins at interfaces have been widely studied due to their important role in the construction of biosensors,bioelectronics and biofuel cells.Interfacial electric field is one of the important factors which could affect the adsorption and bioactivity of proteins at materials surfaces.It could dramatically change the adsorption density,molecular conformation and orientation at material surfaces.In this paper,the influence of interfacial electric field on the adsorption kinetics and bioactivity of hemoglobin(Hb) on a three-dimensional(3D) macroporous gold electrode surface has been studied using electrochemical methods and infrared spectroscopy.It was found that the interfacial electric field created excess surface charge which would accelerate the adsorption rate of Hb on the substrate by the enhanced electrostatic interactions between the electrode and protein patches.However,higher interfacial electric field could damage the conformation of the adsorbed Hb molecules,resulting in loss of the catalytic activity towards the reduction of hydrogen peroxide.Only at a surface with zero charge,the conformation and bioactivity of the adsorbed Hb molecules can be well retained.This work would provide fundamentals for the construction of biosensors,bioelectronics and biofuel cells,and assist to understand the interfacial behavior of biomolecules on charged biological interfaces.
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