Huang Chao, Liu Rui, Ding Yue, Zhao Linlin, Zhu Zongmin, Li Qiyan, Jiang Dafeng, Wu Yuxin, Yu Xuemei, Ding Shengyong, Gao Xibao, Zhu Riran
The First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, 250355, PR China; Department of Pharmacy, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan 250014, PR China.
Nanchang Center for Disease Control and Prevention, Nanchang, PR China; Department of Physical and Chemical Inspection, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan 250000, PR China.
Spectrochim Acta A Mol Biomol Spectrosc. 2025 Apr 5;330:125702. doi: 10.1016/j.saa.2025.125702. Epub 2025 Jan 4.
The sensitive and accurate detection of copper ions is crucial for public health, medical research, and environmental monitoring. In this study, we developed a sensor based on template-assembly activation of the primer exchange reaction (PER) for the on-site detection of copper ions in blood. Copper ions triggered the assembly of two template fragments into a hairpin structure via a click-chemistry reaction, activating the PER. Polymerase then repeatedly guided the polymerization of multiple primers along the assembled PER template, generating amplified products containing G-triplex sequences. These G-triplex structures specifically enhanced the fluorescence of thioflavin T and exhibited peroxidase-like activity, serving as dual-functional signal reporters for both fluorescence and colorimetric outputs. The sensor effectively amplified a single copper ion signal into multiple G-triplex signals, achieving high sensitivity with detection limits of 68.5 nM in fluorescence mode and 70.4 nM in colorimetric mode. The system also demonstrated strong selectivity, due to the high specificity of the click-chemistry reaction for copper ions. The dual-mode detection minimized false signals and improved accuracy through cross-verification. Additionally, both fluorescence and colorimetric signals were easily measurable without complex instrumentation, enabling flexible application. The method was successfully applied to blood samples, showcasing its robust performance. This sensor offers a promising alternative for copper ion detection with broad potential applications in public health, medical research, and environmental monitoring.
铜离子的灵敏准确检测对于公共卫生、医学研究和环境监测至关重要。在本研究中,我们开发了一种基于引物交换反应(PER)模板组装激活的传感器,用于现场检测血液中的铜离子。铜离子通过点击化学反应触发两个模板片段组装成发夹结构,激活PER。然后聚合酶沿着组装好的PER模板反复引导多个引物的聚合,产生包含G-四链体序列的扩增产物。这些G-四链体结构特异性增强硫黄素T的荧光并表现出类似过氧化物酶的活性,作为荧光和比色输出的双功能信号报告分子。该传感器有效地将单个铜离子信号放大为多个G-四链体信号,在荧光模式下检测限为68.5 nM,比色模式下检测限为70.4 nM,实现了高灵敏度。由于点击化学反应对铜离子的高特异性,该系统还表现出很强的选择性。双模式检测通过交叉验证最小化了假信号并提高了准确性。此外,荧光和比色信号无需复杂仪器即可轻松测量,实现了灵活应用。该方法成功应用于血液样本,展示了其强大的性能。这种传感器为铜离子检测提供了一种有前景的替代方法,在公共卫生、医学研究和环境监测中具有广泛的潜在应用。