化学
点击化学
荧光
链霉亲和素
检出限
铜
生物素
基质(水族馆)
叠氮化物
荧光显微镜
分析化学(期刊)
纳米技术
色谱法
组合化学
有机化学
生物化学
材料科学
物理
海洋学
量子力学
地质学
作者
Chenchen Ge,Xiong Chen,Dou Wang
出处
期刊:Talanta
[Elsevier BV]
日期:2024-03-22
卷期号:274: 125973-125973
被引量:5
标识
DOI:10.1016/j.talanta.2024.125973
摘要
Sensitive detection of copper ion (Cu2+), which is of great importance for environmental pollution and human health, is crucial. In this study, we present a highly sensitive method for measuring Cu2+ in an array of femtoliter wells. In brief, magnetic beads (MBs) modified with alkyne groups were bound to the azide groups of biotin-PEG3-azide (bio-PEG-N3) via Cu+-catalyzed click chemistry. Cu+ in the click chemistry reaction was generated by reducing Cu2+ with sodium ascorbate. Following the ligation, the surface of the MBs was modified with biotin, which could be labeled with streptavidin-β-galactosidase (SβG). The MBs complex was then suspended in β-galactosidase substrate fluorescein-di-β-d-galactopyranoside (FDG), and loaded into the array of femtoliter wells. The MBs sank into the wells due to gravity, and the resulting fluorescent product, generated from the reaction between SβG on the surface of the MBs and FDG, was confined within the wells. The number of fluorescent wells increased with higher Cu2+ concentrations. The bright-field and fluorescent images of the wells were acquired using an inverted fluorescent microscope. The detection limit of this assay for Cu2+ was 1 nM without signal amplification, which was 103 times lower than that of traditional fluorescence detection assays.
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