Seifner Alexandra, Lieberzeit Peter, Jungbauer Christof, Dickert Franz L
University of Vienna, Department of Analytical Chemistry and Food Chemistry, Währinger Strasse 38, 1090 Vienna, Austria.
Anal Chim Acta. 2009 Oct 5;651(2):215-9. doi: 10.1016/j.aca.2009.08.021. Epub 2009 Aug 21.
Surface imprinting techniques with erythrocytes as templates yield polymer coatings with selective recognition sites towards red blood cells. The resulting cavities in the respective surface exhibit selectivity between blood subgroups as shown by Quartz Crystal Microbalance (QCM) measurements. Mass sensitive effects in the kilohertz range could be observed for concentrations down to 0.5 x 10(8) cells/mL. Frequency response as well as recovery of the sensor took place within a few minutes, indicating that no covalent binding is involved. Linear concentration dependence over a defined region provides ideal conditions for cross selectivity measurements. A1 imprinted sensor coatings resulted in an effect of 40 kHz when exposed to the template blood group, while A2 erythrocytes yielded just 11% of that value on the same layer. Furthermore, A2 imprinted coatings incorporated only one third the amount of A1 erythrocytes as compared to A2 ones. Therefore, imprinted materials depict the entire cell surface and utilize it for recognition, whereas natural antibodies bind on the defined antigen position and thus usually cannot distinguish between cells carrying different amounts of them.
以红细胞为模板的表面印迹技术可制备出对红细胞具有选择性识别位点的聚合物涂层。如石英晶体微天平(QCM)测量所示,在相应表面形成的空穴对不同血型亚组具有选择性。对于低至0.5×10⁸个细胞/毫升的浓度,可观察到千赫兹范围内的质量敏感效应。传感器的频率响应以及恢复在几分钟内即可完成,这表明不存在共价结合。在定义区域内的线性浓度依赖性为交叉选择性测量提供了理想条件。A1印迹传感器涂层在暴露于模板血型时产生了40 kHz的效应,而A2红细胞在同一层上产生的效应仅为该值的11%。此外,与A2印迹涂层相比,A1印迹涂层结合的A2红细胞数量仅为其三分之一。因此,印迹材料描绘了整个细胞表面并将其用于识别,而天然抗体则结合在特定的抗原位置上,因此通常无法区分携带不同数量抗原的细胞。