【摘要】 生物分子固定化或传感界面设计技术是研制压电免疫传感器的关键之一 .本文结合自组装单分子膜 (SAMs)和聚电解质静电吸附组装技术 ,提出了一种新的压电免疫传感器中生物分子固定化方法 ,研制成一种检测补体C3的压电免疫传感器 .先在石英晶振的金电极表面组装一层胱胺SAMs,再在膜上组装带相反电荷的聚苯磺酸钠 (PSS)单层膜 ,通过静电吸附作用固定抗体 (抗原 ) ,实现对相应抗原 (抗体 )的检测 .利用扫描电镜技术 ,从形态上考察了晶振组装胱氨SAMs与PSS及固定补体C3 抗体后的表面形貌 .研究了抗体的固定化条件 ,探讨了传感器采用这种固定化方法的响应与再生性能 ,并与戊二醛键合固定法进行比较 .结果表明 ,这种固定化方法不仅对蛋白质类生物分子的固定化具有普适性 ,而且对所固定的生物分子的活性影响小 ,传感器响应的频移值大 ,灵敏度高 ,选择性和再生性能均较好更多还原

【Abstract】 The immobilization of biomolecules or the design technology of sensing interface is one of the key factors for piezoelectric immunosensors. In this paper, two technologies named as the self-assembled monolayers (SAMs) and the opposite-charged polyelectrolyte adsorption are combined for a novel immobilization of protein molecules applied to an immunosensor for detecting complement C 3 in human serum. An opposite-charged polystyrenesulfonate (PSS) layer forms on the cystamine (Cys) self-assembled monolayers (SAMs) on the surface of the quartz crystal microbalance (QCM) which electrostatically adsorbs antibodies of complement C 3 (anti-C 3) onto the QCM for immunoreacting complement C 3. The surface morphologies of the QCM were investigated by scanning electron microscopy (SEM) after being modified with Cys SAMs and PSS layer and then immobilizing anti-C 3, respectively. The conditions of self-assembling Cys SAMs and PSS layer as well as immobilizing anti-C 3 are optimized in detail. Compared to the glutaraldehyde binding approach, the antibodies immobilized by the PSS adsorption procedure present higher antibody activity in terms of greater frequency response to immunoreaction. It is found that this immunosensing system provides advantages of improved sensitivity, selectivity and reusability. The immobilization method developed here might offer a promising possibility in firmly immobilizing biomolecules for biosensors.更多还原