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Colorimetric Detection of Copper(II) Ion Using Click Chemistry and Hemin/G-Quadruplex Horseradish Peroxidase-Mimicking DNAzyme

机译:用点击化学和Hemin / G四联辣根过氧化物酶模拟DNA酶比色检测铜离子

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摘要

G-quadruplex-forming sequence can be formed through a copper(I) ion (Cu~+)-catalyzed click chemistry between azide- and alkyne-modified short G-rich sequences in aqueous solution, eliminating immobilization and washing steps of conventional assays. The source for Cu~+ was generated from the reduction of Cu~(2+) with the reductant of sodium ascorbate. In the presence of hemin and K~+, the self-assembly of hemin/G-quadruplex structure has the activity of horse-radish peroxidase (HRP), which can catalyze its colorless substrate tetrazmethyl benzidine (TMB) into a colored product. Hence, the concentration of Cu~(2+) can be evaluated visually for qualitative analysis according to the color change of the solution, and the optical density (OD) value of the resulting solution at 450 nm was also recorded using a microplate reader for quantitative analysis.
机译:G-四链体形成序列可通过水溶液中叠氮化物和炔烃修饰的短富G序列之间的铜(I)离子(Cu +)催化的点击化学反应形成,无需常规测定的固定和洗涤步骤。 Cu〜+的来源是由抗坏血酸钠还原剂还原Cu〜(2+)而产生的。在存在血红素和钾离子的情况下,血红素/ G-四链体结构的自组装具有辣根过氧化物酶(HRP)的活性,可将其无色底物四甲基联苯胺(TMB)催化成彩色产物。因此,可以根据溶液的颜色变化目视评估Cu〜(2+)的浓度,以进行定性分析,并使用酶标仪在450 nm处记录所得溶液在450 nm的光密度(OD)值。定量分析。

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