Li Ping, Ge Bixia, Ou Lily M-L, Yao Zhihui, Yu Hua-Zhong
Department of Chemistry, Simon Fraser University, 8888 University Drive, Burnaby, BC V5A 1S6, Canada.
Biogate Laboratories Ltd., 110-4238 Lozells Avenue, Burnaby, BC V5A 0C4, Canada.
Sensors (Basel). 2015 Aug 20;15(8):20543-56. doi: 10.3390/s150820543.
A simple DNA-redox cation interaction enhancement strategy has been developed to improve the sensitivity of electrochemical immunosensors for protein detection. Instead of labeling with fluorophores or redox-active groups, the detection antibodies were tethered with DNA single strands. Based on the electrostatic interaction between redox cations (Ru(NH3)6) and negatively charged DNA backbone, enhanced electrochemical signals were obtained. Human chorionic gonadotropin (hCG) detection has been performed as a trial analysis. A linear response range up to the concentration of 25 mIU/mL and a detection limit of 1.25 mIU/mL have been achieved, both are comparable with the ultrasensitive enzyme-linked immunosorbent assay (ELISA) tests. The method also shows great selectivity towards hCG over other hormones such as thyroid stimulating hormone (TSH) and follicle stimulating hormone (FSH). By and large, our approach bears the merits of cost effectiveness and simplicity of instrumentation in comparison with conventional optical detection methods.
已开发出一种简单的DNA-氧化还原阳离子相互作用增强策略,以提高用于蛋白质检测的电化学免疫传感器的灵敏度。检测抗体未用荧光团或氧化还原活性基团标记,而是与DNA单链相连。基于氧化还原阳离子(Ru(NH3)6)与带负电荷的DNA主链之间的静电相互作用,获得了增强的电化学信号。已进行人绒毛膜促性腺激素(hCG)检测作为试验分析。实现了高达25 mIU/mL浓度的线性响应范围和1.25 mIU/mL的检测限,两者均与超灵敏酶联免疫吸附测定(ELISA)测试相当。该方法对hCG的选择性也远高于其他激素,如促甲状腺激素(TSH)和促卵泡激素(FSH)。总体而言,与传统光学检测方法相比,我们的方法具有成本效益高和仪器简单的优点。