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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Characterization of dansylated glutathione, glutathione disulfide, cysteine and cystine by narrow bore liquid chromatography/electrospray ionization mass spectrometry
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Characterization of dansylated glutathione, glutathione disulfide, cysteine and cystine by narrow bore liquid chromatography/electrospray ionization mass spectrometry

机译:窄孔液相色谱/电喷雾电离质谱法表征丹磺酰谷胱甘肽,二硫谷胱甘肽,半胱氨酸和胱氨酸

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摘要

A method using reversed phase high performance liquid chromatography/electrospray ionization-mass spectrometry (RP-LC/ESI-MS) has been developed to confirm the identity of dansylated derivatives of cysteine (C) and glutathione (GSH), and their respective dimers, cystine (CSSC) and glutathione disulfide (GSSG), Cysteine, GSH, CSSC and GSSG are present at low concentrations in rainbow trout (Oncorhynchus mykiss) liver cells. Initially, hepatic cells were sampled from a suspension culture and disrupted upon addition of 10% perchloric acid. The reduced thiols present in the cell extracts were acetylated to prevent dimerization and then the C and GSH species were derivatized,vith dansyl chloride for fluorescence detection, An LC system using a weak anion exchange column (AE) with fluorescence detection (FLD) was used for sensitive routine analysis; however, it produced peaks of unknown origin in addition to the expected analytes. Analytes were then separated on a C18 RP-LC system using a water/acetonitrile gradient with 0.2% formic acid, and detected using LC/ESI-MS at 3.5 KV which produced an intense ion with a minimum limit of detection of less than 0.5 pmole injected (>10:1 signal-to-noise (S/N). Subsequently, fractions of effluent from the AE-LC/FLD system were analyzed by LC/ESI-MS to confirm the presence of the target analytes in routine cell extracts. Monodansylated GSSG was identified as a product that could possibly affect the quantification of GSH and GSSG, Copyright (C) 2000 John Wiley & Sons, Ltd. [References: 12]
机译:已开发出一种使用反相高效液相色谱/电喷雾电离质谱(RP-LC / ESI-MS)的方法,以确认半胱氨酸(C)和谷胱甘肽(GSH)的丹磺化衍生物及其各自的二聚体的身份,虹鳟(Oncorhynchus mykiss)肝细胞中的胱氨酸(CSSC)和谷胱甘肽二硫化物(GSSG),半胱氨酸,GSH,CSSC和GSSG含量低。最初,从悬浮培养物中取样肝细胞,并在加入10%高氯酸后破坏。将细胞提取物中存在的还原硫醇乙酰化以防止二聚化,然后将C和GSH物种衍生化,用丹酰氯进行荧光检测,使用LC系统,使用弱阴离子交换柱(AE)和荧光检测(FLD)用于敏感的常规分析;但是,除预期的分析物外,它还会产生未知来源的峰。然后在C18 RP-LC系统上使用0.2%甲酸的水/乙腈梯度分离分析物,并使用LC / ESI-MS在3.5 KV的条件下进行检测,产生的强离子最低检出限小于0.5 pmole进样(> 10:1信噪比(S / N)。随后,通过LC / ESI-MS分析AE-LC / FLD系统的流出物部分,以确认常规细胞提取物中目标分析物的存在。单丹磺酰化的GSSG被确定为可能影响GSH和GSSG定量的产品,版权所有(C)2000 John Wiley&Sons,Ltd. [参考文献:12]

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