Tai Dar-Fu, Lin Chung-Yin, Wu Tzong-Zeng, Chen Li-Kuang
Department of Chemistry and Institute of Biotechnology, National Dong-Hwa University, Hualien, Taiwan.
Anal Chem. 2005 Aug 15;77(16):5140-3. doi: 10.1021/ac0504060.
Molecularly imprinted film was fabricated in the presence of a pentadecapeptide onto a quartz crystal microbalance (QCM) chip. This 15-mer peptide has been known as the linear epitope of the dengue virus NS1 protein. Imprinting resulted in an increased polymer affinity toward the corresponding templates but also to the virus protein. Direct detection of the dengue virus protein was achieved quantitatively. The QCM chip response to the NS1 protein was obtained using epitope-mediated imprinting demonstrating a comparable frequency shift in chips immobilized with monoclonal antibodies. The binding effect was further enhanced and confirmed using a monoclonal antibody to form a sandwich with the MIP-NS1 protein complex on the chip. No pretreatment was required.
在一个十五肽存在的情况下,在石英晶体微天平(QCM)芯片上制备了分子印迹膜。这种十五肽已知是登革病毒NS1蛋白的线性表位。印迹导致聚合物对相应模板以及病毒蛋白的亲和力增加。实现了对登革病毒蛋白的直接定量检测。使用表位介导的印迹获得了QCM芯片对NS1蛋白的响应,这表明在固定有单克隆抗体的芯片中具有可比的频率偏移。使用单克隆抗体进一步增强并确认了结合效果,以在芯片上与MIP-NS1蛋白复合物形成夹心结构。无需进行预处理。