State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, PR China.
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, PR China.
Biosens Bioelectron. 2021 Nov 15;192:113547. doi: 10.1016/j.bios.2021.113547. Epub 2021 Aug 8.
Herein, a photocurrent polarity switching platform for highly selective assay of mucin 1 (MUC1) was developed based on target-induced hemin transfer from ZrO hollow spheres (ZrO HSs) to G-quadruplex nanowires (G wires). In this system, SiO spheres were used as templates to synthesize the uniform and mesoporous ZrO HSs. As nanocontainers, ZrO HSs could load hemin in its cavity via pores. Then, the aptamers of MUC1, as bio-gates, blocked the pores of ZrO HSs based on the specific binding of Zr and the phosphate groups of aptamer. In the presence of MUC1, the aptamer could specifically recognize and bind with MUC1, and then leave away from the surface of ZrO HSs, which resulted in the opening of the bio-gates and releasing of hemin. Assisted with the G wires formed on the Au NPs/InS/ITO, the released hemin was captured on the electrode through the formation of hemin/G-quadruplex structure, leading to the switch of the photocurrent polarity of the electrode from anodic photocurrent to cathodic photocurrent. The proposed photoelectrochemical biosensor showed outstanding performance for MUC1 assay with high selectivity, wide linear response range (1 fg mL -10 ng mL) and lower detection limit (0.48 fg mL). And the strategy could be easily extended to a triple-mode detection of MUC1 because the hemin/G-quadruplex structure was widely used in electrochemical and colorimetric methods as a hydrogen peroxide mimetic enzyme, which might provide wide applications in biological or clinical studies.
在此,我们基于血红素从 ZrO 空心球(ZrO HSs)向 G-四链体纳米线(G 线)的目标诱导转移,开发了一种用于高选择性检测黏蛋白 1(MUC1)的光电流极性切换平台。在该体系中,我们使用 SiO 球作为模板合成了均匀且具有介孔的 ZrO HSs。作为纳米容器,ZrO HSs 可以通过孔道负载血红素。然后,MUC1 的适体作为生物门,基于 Zr 与适体的磷酸基团的特异性结合,阻断 ZrO HSs 的孔道。在存在 MUC1 的情况下,适体能特异性识别并与 MUC1 结合,然后从 ZrO HSs 表面离开,从而导致生物门打开并释放血红素。在 Au NPs/InS/ITO 上形成的 G 线的辅助下,释放的血红素通过血红素/G-四链体结构的形成被捕获在电极上,导致电极的光电流极性从阳极光电流切换为阴极光电流。所提出的光电化学生物传感器在 MUC1 检测方面表现出出色的性能,具有高选择性、宽线性响应范围(1 fg mL-10 ng mL)和较低的检测限(0.48 fg mL)。并且,由于血红素/G-四链体结构作为过氧化物酶模拟物广泛应用于电化学和比色法中,该策略可以很容易地扩展到 MUC1 的三模态检测,这可能为生物或临床研究提供广泛的应用。