Anhui key laboratory of Chem-Biosensing, School of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241000, PR China.
Analyst. 2013 Apr 21;138(8):2456-62. doi: 10.1039/c3an36775d.
A quartz crystal microbalance (QCM) biosensor for theophylline was developed by recognition of RNA aptamer and gold nanoparticle amplification technique. Firstly, a designed small single-stranded RNA, RNA1, was immobilized onto the QCM electrode through a thiol linker. Then, the complementary stranded RNA2, which can combine with RNA1 to form a double-stranded RNA with a recognition unit of theophylline, could be self-assembled on the QCM electrode surface through a hybrid reaction in the presence of theophylline. The recognition process could cause a frequency change of QCM to give the signal related to theophylline. When RNA2 was tethered to gold nanoparticles, the signal could be amplified to further enhance the sensitivity of the designed sensor. Under the optimal conditions, the QCM-based biosensor showed excellent sensitivity (limit of detection, 8.2 nM) and specificity with a dissociation constant of Kd = 5.26 × 10(-7) M. The sensor can be used to quantitatively detect theophylline in serum, suggesting that it can be applied in complex biological samples.
基于石英晶体微天平(QCM)的茶碱生物传感器通过 RNA 适体识别和金纳米粒子扩增技术开发。首先,将设计的小单链 RNA(RNA1)通过硫醇链接剂固定在 QCM 电极上。然后,互补的 RNA2 可以通过杂交反应在茶碱存在的情况下自组装到 QCM 电极表面,与 RNA1 结合形成具有茶碱识别单元的双链 RNA。识别过程会引起 QCM 的频率变化,从而给出与茶碱相关的信号。当 RNA2 连接到金纳米粒子上时,信号可以被放大,从而进一步提高设计传感器的灵敏度。在最佳条件下,基于 QCM 的生物传感器具有出色的灵敏度(检测限为 8.2 nM)和特异性,解离常数为 Kd = 5.26 × 10(-7) M。该传感器可用于定量检测血清中的茶碱,表明它可应用于复杂的生物样本。