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Determination of thiols and disulfides via HPLC quantification of 5-thio-2-nitrobenzoic acid.

机译:通过HPLC定量5-硫代-2-硝基苯甲酸测定硫醇和二硫化物。

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This work presents an assay for total thiols and total disulfides in biological samples via HPLC quantification of 5-thio-2-nitrobenzoic acid (TNB) derived from the reaction of thiols with 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB, Ellman's reagent). This method also provides simultaneous quantification of glutathione (GSH) via the measurement of the GSH-DTNB adduct (GSH-TNB). By using 326nm as the detecting wavelength, the HPLC detection limit for TNB and the GSH-TNB adduct was determined to be 15 and 7.5pmol respectively. A recovery study with OVCAR-3 cells revealed that the recovery yields for TNB in the procedures for determining non-protein thiols, protein thiols, non-protein disulfides, and protein disulfides were 99.4+/-1.2% (n=3), 98.1+/-5.0% (n=3), 95.6+/-0.9% (n=3), and 96.6+/-2.3% (n=3) respectively. The recovery yield for GSH-TNB in the procedures for determining non-protein thiols, protein thiols, non-protein disulfides, and protein disulfides was 99.0+/-0.3% (n=3), 95.1+/-4.9% (n=3), 96.8+/-0.6% (n=3), and 95.1+/-2.9% (n=3) respectively. The reproducibility, expressed as the relative standard deviation for the analyte, for TNB was determined to be 2.8% (n=6) for non-protein thiols, 3.9% (n=6) for protein thiols, 3.6% (n=6) for non-protein disulfides and 4.6% (n=6) for protein disulfides. The reproducibility for GSH-TNB was determined to be 1.6% (n=6) for non-protein thiols and 2.6% (n=6) for non-protein disulfides. By comparing the amount of GSH determined in a biological sample before NaBH(4) reduction with that after the reduction, this method can provide information associated with thiol glutathionylation which would be useful for protein glutathionylation study. This method should be applicable to cellular, subcellular, protein, or other biomatrix samples for thiol and disulfide quantification and will be a useful analytical method in the study of thiol redox state and thiol glutathionylation.
机译:这项工作通过HPLC定量分析了硫醇与5,5'-二硫代双(2-硝基苯甲酸)(DTNB)衍生的5-硫-2-硝基苯甲酸(TNB)对生物样品中的总硫醇和总二硫化物进行了测定,埃尔曼试剂)。该方法还可以通过测量GSH-DTNB加合物(GSH-TNB)同时定量谷胱甘肽(GSH)。通过使用326nm作为检测波长,TNB和GSH-TNB加合物的HPLC检测限分别为15和7.5pmol。 OVCAR-3细胞的回收率研究表明,在确定非蛋白硫醇,蛋白硫醇,非蛋白二硫化物和蛋白二硫化物的程序中,TNB的回收率为99.4 +/- 1.2%(n = 3),98.1分别为+/- 5.0%(n = 3),95.6 +/- 0.9%(n = 3)和96.6 +/- 2.3%(n = 3)。在测定非蛋白质硫醇,蛋白质硫醇,非蛋白质二硫键和蛋白质二硫键的程序中,GSH-TNB的回收率分别为99.0 +/- 0.3%(n = 3),95.1 +/- 4.9%(n = 3),96.8 +/- 0.6%(n = 3)和95.1 +/- 2.9%(n = 3)。对于TNB的重现性表示为分析物的相对标准偏差,对于非蛋白质硫醇而言,确定为2.8%(n = 6),对于蛋白质硫醇而言为3.9%(n = 6),对于3.6%(n = 6)对于非蛋白质二硫化物为4.6%(n = 6)。对于非蛋白硫醇,GSH-TNB的重现性确定为1.6%(n = 6),对于非蛋白二硫化物为2.6%(n = 6)。通过比较在NaBH(4)还原之前和还原后的生物样品中测定的GSH量,该方法可以提供与巯基谷胱甘肽化有关的信息,这对蛋白质谷胱甘肽化研究很有用。此方法应适用于细胞,亚细胞,蛋白质或其他生物基质样品中的硫醇和二硫键定量,将是研究硫醇氧化还原状态和硫醇谷胱甘肽化的有用分析方法。

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