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采用 HPLC 在线同位素稀释电感耦合等离子体质谱法对健康人群血清蛋白质中的硒进行高通量定量分析。

High-throughput quantification of selenium in individual serum proteins from a healthy human population using HPLC on-line with isotope dilution inductively coupled plasma-MS.

机构信息

Environmental Chemical Processes Laboratory, Department of Chemistry, University of Crete, Crete, Greece.

出版信息

Proteomics. 2010 Oct;10(19):3447-57. doi: 10.1002/pmic.200900677.

Abstract

In this study, a method, based on dual column affinity chromatography hyphenated to isotope dilution inductively coupled plasma-quadrupole MS, was developed for selenium determination in selenoprotein P, glutathione peroxidase, and selenoalbumin in human serum samples from a group of healthy volunteers (n=399). Method improvement was achieved using methanol-enhanced isotope dilution which resulted in improved sensitivity and removal of isobaric interferences. Although no human serum reference materials are currently certified for their selenium species levels, method development was conducted using human serum reference material BCR 637 and 639 as their Se species content has been reported in the previous studies, and thus comparisons were possible. The mean selenium concentrations determined for the 399 healthy volunteer serum samples were 23 ± 10 ng Se mL(-1) for glutathione peroxidase, 49 ± 15 ng Se mL(-1) for selenoprotein P and 11 ± 4 ng Se mL(-1) for selenoalbumin. These values are found to be in close agreement with published values for a limited number of healthy volunteer samples, and to establish baseline Se levels in serum proteins for an apparently healthy group of individuals, thus allowing for subsequent comparisons with respective values determined for groups of individuals with selenium related health issues, as well as assist in the discovery of potential selenium biomarkers. Also, the relationship between Se serum protein levels and some anthropometric characteristics of the volunteer population were investigated. Additionally, further development of the analytical method used in this study was achieved by adding a size exclusion chromatography column after the two affinity columns via a switching valve. This allowed for the separation of small selenium-containing molecules from glutathione peroxidase and thus enhanced the overall confidence in its identification.

摘要

在这项研究中,开发了一种基于双柱亲和色谱与同位素稀释电感耦合等离子体质谱联用的方法,用于测定来自一组健康志愿者(n=399)血清样本中硒蛋白 P、谷胱甘肽过氧化物酶和白蛋白中的硒。使用甲醇增强的同位素稀释方法提高了灵敏度并去除了同量异位素干扰,从而实现了方法的改进。尽管目前没有针对其硒形态水平的人类血清参考物质进行认证,但使用人血清参考物质 BCR 637 和 639 进行了方法开发,因为它们的硒形态含量已在之前的研究中报道过,因此可以进行比较。对于 399 个健康志愿者血清样本,测定的平均硒浓度分别为:谷胱甘肽过氧化物酶为 23±10ng Se mL(-1),硒蛋白 P 为 49±15ng Se mL(-1),白蛋白为 11±4ng Se mL(-1)。这些值与发表的有限数量的健康志愿者样本的值非常吻合,为血清蛋白质中的硒水平建立了基线,从而可以与具有硒相关健康问题的个体的相应值进行后续比较,也有助于发现潜在的硒生物标志物。此外,还研究了硒血清蛋白水平与志愿者人群的一些人体测量特征之间的关系。此外,通过在两个亲和柱后通过切换阀添加一个尺寸排阻色谱柱,进一步开发了本研究中使用的分析方法。这允许将含有硒的小分子与谷胱甘肽过氧化物酶分离,从而提高了其鉴定的整体可信度。

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