Chen Peiwu, Jiang Lan, Xie Xianjin, Sun Dong, Liu Jinyao, Zhao Yuefeng, Li Yuhao, Balbín Tamayo Abel Ibrahim, Liu Baolin, Miao Yuqing, Ouyang Ruizhuo
Institute of Bismuth and Rhenium Science, School of Materials and Chemistry, University of Shanghai for Science and Technology Shanghai 200093 China
School of Chemistry and Chemical Engineering, Henan Normal University Xinxiang 453007 China.
RSC Adv. 2022 Apr 19;12(19):11867-11876. doi: 10.1039/d2ra01047j. eCollection 2022 Apr 13.
Pt@CeO nanospheres (NSs) were first synthesized by simply mixing Ce(NO) and KPtCl under the protection of pure argon at 70 °C for 1 h, which exhibited excellent catalytic ability toward hydrogen peroxide (HO). An electrochemical biosensor was successfully developed using Pt@CeO NSs as a capture probe for the ultra-sensitive and fast detection of miRNA-21, a new type of biomarker for disease diagnostics, especially for cancer. During the step-by-step construction process of the RNA sensor, Pt@CeO NSs were functionalized with streptavidin (SA) to obtain SA-Pt@CeO NSs through amide bonds. Gold nanoparticles (Au NPs) were electrodeposited on the surface of the glassy carbon electrode to improve the transmission capacity of electrons and provided Au atoms for fixing the thiolated capture probe (SH-CP) with a hairpin structure on the electrode forming Au-S bonds. The target miRNA-21 specifically hybridized with SH-CP and opened the hairpin structure to form a rigid duplex so as to activate the biotin at the end of the capture probe. SA-Pt@CeO NSs were thus specially attached to the electrode surface through the biotin-streptavidin affinity interaction, finally leading to the significant signal amplification. The ultra-sensitive and rapid detection of miRNA-21 was finally realized as expected benefiting from the excellent catalytic ability of Pt@CeO NSs toward HO in a wide linear concentration range from 10 fM to 1 nM with the detection limit as low as 1.41 fM. The results achieved with this new RNA sensor were quite satisfactory during the blood sample analysis.
首先,通过在70℃纯氩气保护下将Ce(NO)和KPtCl简单混合1小时,合成了Pt@CeO纳米球(NSs),其对过氧化氢(H₂O₂)表现出优异的催化能力。利用Pt@CeO NSs作为捕获探针,成功开发了一种用于超灵敏快速检测miRNA - 21的电化学生物传感器,miRNA - 21是一种新型疾病诊断生物标志物,尤其用于癌症诊断。在RNA传感器的逐步构建过程中,Pt@CeO NSs用链霉亲和素(SA)进行功能化,通过酰胺键获得SA - Pt@CeO NSs。在玻碳电极表面电沉积金纳米颗粒(Au NPs)以提高电子传输能力,并提供Au原子用于在电极上固定具有发夹结构的硫醇化捕获探针(SH - CP),形成Au - S键。目标miRNA - 21与SH - CP特异性杂交并打开发夹结构形成刚性双链体,从而激活捕获探针末端的生物素。SA - Pt@CeO NSs因此通过生物素 - 链霉亲和素亲和相互作用特异性地附着在电极表面,最终导致显著的信号放大。由于Pt@CeO NSs在10 fM至1 nM的宽线性浓度范围内对H₂O₂具有优异的催化能力,检测限低至1.41 fM,最终如预期实现了miRNA - 21的超灵敏快速检测。在血样分析中,这种新型RNA传感器获得的结果相当令人满意。