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通过表面增强拉曼光谱法轻松且灵敏地测量细胞中的 GSH/GSSG。

Facile and sensitive measurement of GSH/GSSG in cells by surface-enhanced Raman spectroscopy.

机构信息

State Key Laboratory of Toxicology and Medical Countermeasures, And Laboratory of Toxicant Analysis, Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing, 100850, China; Currently Work at National Center of Biomedical Analysis, Beijing, 100850, China.

State Key Laboratory of Toxicology and Medical Countermeasures, And Laboratory of Toxicant Analysis, Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing, 100850, China.

出版信息

Talanta. 2021 Mar 1;224:121852. doi: 10.1016/j.talanta.2020.121852. Epub 2020 Nov 13.

Abstract

Reduced glutathione (GSH) and the oxidized glutathione (GSSG) are well-known biomolecules in the main constituents of intracellular redox homeostasis system. A rapid, accurate measurement of cellular GSH and GSSG is quite needed in investigating important biochemical events. In this work, we present a novel and sensitive method to monitor intracellular GSH and GSSG concentrations by a portable surface-enhanced Raman spectroscopy (SERS) technique. We introduced a reduction-sensitive reaction-type Raman probe, 5,5'-dithiobis-(2-nitrobenzoic acid) (DTNB) to initiate GSH reduction, itself concomitantly converts to 2-nitro-5-thiobenzoic acid (TNB) to release a strong SERS signal. In a convenient way of inorganic salt MgSO induced aggregation of silver nanoparticles substrate, we easily implemented a good discrimination between DTNB and TNB, and a quantitative measurement of GSH and GSSG with a high sensitivity of 10 nM. This SERS method proved its feasible applicability in rapidly and sensitively monitoring GSH depletion behaviors of some notorious alkylating agents, i.e., sulfur mustard and nitrogen mustards in ex vitro or in vitro (cellular response). This SERS method may be very worthwhile in cellular detoxication event via the GSH approach and other GSH involved biomedical researches.

摘要

还原型谷胱甘肽 (GSH) 和氧化型谷胱甘肽 (GSSG) 是细胞内氧化还原稳态系统的主要组成部分中众所周知的生物分子。在研究重要的生化事件时,快速、准确地测量细胞内 GSH 和 GSSG 的浓度是非常必要的。在这项工作中,我们提出了一种新的、敏感的方法,通过便携式表面增强拉曼光谱 (SERS) 技术来监测细胞内 GSH 和 GSSG 的浓度。我们引入了一种还原敏感的反应型拉曼探针,5,5'-二硫代双(2-硝基苯甲酸) (DTNB) 来引发 GSH 的还原,同时自身转化为 2-硝基-5-硫代苯甲酸 (TNB) 以释放出强的 SERS 信号。在一种方便的无机盐 MgSO 诱导银纳米粒子基底聚集的方法中,我们很容易实现了 DTNB 和 TNB 的良好区分,并以 10 nM 的高灵敏度对 GSH 和 GSSG 进行定量测量。该 SERS 方法在快速、敏感地监测一些臭名昭著的烷化剂(如硫芥和氮芥)在体外或体外(细胞反应)中 GSH 耗竭行为方面表现出了可行的适用性。该 SERS 方法可能在通过 GSH 途径和其他涉及 GSH 的生物医学研究中的细胞解毒事件中具有很高的应用价值。

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