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基于汞离子猝灭荧光金纳米簇的阻断作用的用于检测生物硫醇的无标记方法。

A label-free method for detecting biological thiols based on blocking of Hg2+-quenching of fluorescent gold nanoclusters.

机构信息

Department of Chemical and Biomolecular Engineering (BK21 Program), KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon 305-701, Republic of Korea.

出版信息

Biosens Bioelectron. 2013 Jul 15;45:65-9. doi: 10.1016/j.bios.2013.01.047. Epub 2013 Feb 4.

Abstract

A novel, label-free, fluorescent, turn-on sensor for biological thiol detection that uses highly fluorescent gold nanoclusters (AuNCs), prepared by a bovine serum albumin (BSA)-templated green synthetic route, has been developed. The assay relies on blocking Hg(2+)-induced quenching of the fluorescence of AuNCs, caused by metallophilic Hg(2+)-Au(+) interactions, through selective coordination of biological thiols with Hg(2+) ions. Biological thiols entrap added Hg(2+) ions via a robust Hg-S interaction. This phenomenon prevents Hg(2+)-induced quenching and results in fluorescence from AuNCs. By employing this turn-on sensor, biological thiols, such as cysteine (Cys), glutathione (GSH) and homocysteine (Hcy), are successfully detected at concentrations as low as 8.3 nM for Cys, 9.4 nM for GSH, and 14.9 nM for Hcy. The diagnostic capability and potential in practical applications of this method have been demonstrated by detecting biological thiols in human blood serum.

摘要

一种新颖的、无标记的、荧光、开启型传感器,用于生物硫醇检测,它使用了高度荧光的金纳米簇(AuNCs),通过牛血清白蛋白(BSA)模板的绿色合成路线制备。该测定依赖于通过生物硫醇与 Hg(2+)离子的选择性配位,阻断 Hg(2+)-诱导的 AuNCs 荧光猝灭,这是由于亲汞的 Hg(2+)-Au(+)相互作用引起的。生物硫醇通过强大的 Hg-S 相互作用捕获添加的 Hg(2+)离子。这种现象阻止了 Hg(2+)-诱导的猝灭,导致 AuNCs 发出荧光。通过采用这种开启型传感器,可以在低至 8.3 nM 的半胱氨酸 (Cys)、9.4 nM 的谷胱甘肽 (GSH)和 14.9 nM 的同型半胱氨酸 (Hcy)的浓度下成功检测到生物硫醇,如半胱氨酸 (Cys)、谷胱甘肽 (GSH)和同型半胱氨酸 (Hcy)。通过检测人血清中的生物硫醇,证明了该方法的诊断能力和实际应用潜力。

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