Sun Kai, Chang Yong, Zhou Binbin, Wang Xiaojin, Liu Lin
Henan Province of Key Laboratory of New Optoelectronic Functional Materials, College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang, Henan, People's Republic of China.
Int J Nanomedicine. 2017 Mar 9;12:1905-1915. doi: 10.2147/IJN.S127957. eCollection 2017.
This article presents a general method for the detection of protein kinase with a peptide-like kinase inhibitor as the bioreceptor, and it was done by converting gold nanoparticles (AuNPs)-based colorimetric assay into sensitive electrochemical analysis. In the colorimetric assay, the kinase-specific aptameric peptide triggered the aggregation of AuNPs in solution. However, the specific binding of peptide to the target protein (kinase) inhibited its ability to trigger the assembly of AuNPs. In the electrochemical analysis, peptides immobilized on a gold electrode and presented as solution triggered together the in situ formation of AuNPs-based network architecture on the electrode surface. Nevertheless, the formation of peptide-kinase complex on the electrode surface made the peptide-triggered AuNPs assembly difficult. Electrochemical impedance spectroscopy was used to measure the change in surface property in the binding events. When a ferrocene-labeled peptide (Fc-peptide) was used in this design, the network of AuNPs/Fc-peptide produced a good voltammetric signal. The competitive assay allowed for the detection of protein kinase A with a detection limit of 20 mU/mL. This work should be valuable for designing novel optical or electronic biosensors and likely lead to many detection applications.
本文介绍了一种以肽样激酶抑制剂作为生物受体检测蛋白激酶的通用方法,该方法通过将基于金纳米颗粒(AuNPs)的比色测定转化为灵敏的电化学分析来实现。在比色测定中,激酶特异性适体肽引发溶液中AuNPs的聚集。然而,肽与靶蛋白(激酶)的特异性结合抑制了其引发AuNPs组装的能力。在电化学分析中,固定在金电极上并以溶液形式呈现的肽共同引发电极表面基于AuNPs的网络结构的原位形成。然而,电极表面肽 - 激酶复合物的形成使肽引发的AuNPs组装变得困难。采用电化学阻抗谱来测量结合事件中表面性质的变化。当在此设计中使用二茂铁标记的肽(Fc - 肽)时,AuNPs/Fc - 肽网络产生了良好的伏安信号。竞争测定法可检测蛋白激酶A,检测限为20 mU/mL。这项工作对于设计新型光学或电子生物传感器具有重要价值,并可能带来许多检测应用。