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一种通过抑制谷胱甘肽修饰的银纳米簇的聚集诱导发射增强来检测三磷酸腺苷的无标记荧光探针,该增强由锌离子引发。

A label-free fluorescent probe for the detection of adenosine 5'‑triphosphate via inhibiting the aggregation-induced emission enhancement of glutathione modified silver nanoclusters triggered by zinc ion.

机构信息

School of Chemistry and Environment, Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine, South China Normal University, Guangzhou 510006, China.

School of Chemistry and Environment, Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine, South China Normal University, Guangzhou 510006, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2019 May 5;214:360-365. doi: 10.1016/j.saa.2019.02.040. Epub 2019 Feb 19.

Abstract

It is important to establish sensitive and simple analysis methods for adenosine 5'‑triphosphate (ATP). A label-free fluorescent probe for the determination of ATP was constructed based on glutathione modified silver nanoclusters (AgNCs/GSH). AgNCs/GSH showed aggregation-induced emission enhancement (AIEE) property in the organic solvent. The effects of metal ions on the fluorescence of AgNCs/GSH were also studied. Only zinc ion enhanced the fluorescence of AgNCs/GSH obviously. This was because Zn coordinated with AgNCs/GSH to cause the aggregation of AgNCs/GSH, which was sufficiently proved by TEM. With the addition of ATP, Zn bound with ATP through ZnOP bond and the binding between Zn and AgNCs/GSH was inhibited. Hence the fluorescence of AgNCs/GSH was decreased with increasing the ATP concentration. The fluorescence response was linear in the ATP concentration range of 1-110 μM, and the detection limit was 0.8 μM. Then this method was successfully applied for determining ATP in the samples of human urine and rat serum, the recoveries were in the range of 97.6%-103%.

摘要

建立用于检测三磷酸腺苷(ATP)的灵敏、简单的分析方法非常重要。本研究基于谷胱甘肽修饰的银纳米簇(AgNCs/GSH)构建了一种用于测定 ATP 的无标记荧光探针。AgNCs/GSH 在有机溶剂中表现出聚集诱导发射增强(AIEE)性质。还研究了金属离子对 AgNCs/GSH 荧光的影响。只有锌离子能明显增强 AgNCs/GSH 的荧光。这是因为 Zn 与 AgNCs/GSH 配位导致 AgNCs/GSH 聚集,这通过 TEM 得到了充分证明。随着 ATP 的加入,Zn 通过 ZnOP 键与 ATP 结合,从而抑制 Zn 与 AgNCs/GSH 之间的结合。因此,随着 ATP 浓度的增加,AgNCs/GSH 的荧光强度降低。在 1-110 μM 的 ATP 浓度范围内,荧光响应呈线性关系,检测限为 0.8 μM。然后,该方法成功应用于人尿和鼠血清样品中 ATP 的测定,回收率在 97.6%-103%范围内。

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