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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Quantification of membrane transporter proteins in human lung and immortalized cell lines using targeted quantitative proteomic analysis by isotope dilution nanoLC-MS/MS
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Quantification of membrane transporter proteins in human lung and immortalized cell lines using targeted quantitative proteomic analysis by isotope dilution nanoLC-MS/MS

机译:用同位素稀释纳米/ MS的靶向定量蛋白质组学分析定量人肺和永生化细胞系中的膜转运蛋白

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Information is needed on the expression of transporters in lung to inform drug development and therapeutic decisions. Much of the information currently available is from semiquantitative gene expression or immunometric densitometry studies reported in the literature. NanoLC-MS/MS (MRM mode) isotope dilution targeted quantitative proteomics was used here to quantify twelve selected transporters in fresh human lung membrane fraction samples and in the membrane fraction of selected immortalized human lung epithelial cell line samples. Fractionation was undertaken by homogenization in crude membrane lysis buffer followed by differential centrifugation of the homogenate. In lung membranes we found OATPs to be the most highly expressed transporters of those measured, followed by PEPT2 and ABCs (P-gp & BCRP). SLC22A transporters (OCTs 2 & 3 and OCTN1) were also found to be expressed. OATP2A1, also known as the prostaglandin transporter, was the most highly expressed transporter, being low in two subjects who were at least occasional smokers. One subject, a non-smoker, had an OATP2A1 concentration that was 8.4 times higher than the next nearest concentration, which itself was higher than the concentration of any other transporter. OATP2A1 is known, from gene expression and animal functional studies, to be present in lung. These results inform the understanding of xenobiotic disposition in the lung and show the distinct profile of transporters in lung compared to other tissues. (C) 2018 Elsevier B.V. All rights reserved.
机译:肺部转运仪表达需要信息,以提供药物发展和治疗决策。目前可用的大部分信息来自文献中报道的半定量基因表达或免疫测量型研究。 Nanolc-MS / MS(MRM模式)同位素稀释靶向定量蛋白质组学在此用于在新鲜人肺膜级分样品中量化12种选定的转运蛋白,并在选定的永生化的人肺上皮细胞系样品中的膜堆叠。通过在粗膜裂解缓冲液中均化进行分馏,然后进行均匀离心。在肺膜中,我们发现燕麦片是测量的最高表达的转运蛋白,其次是Pept2和ABCs(P-GP&BCRP)。还发现SLC22A转运蛋白(10月2和3和OCTN1)表达。 OATP2A1,也称为前列腺素转运蛋白是最表达的运输扣,在至少偶尔吸烟者的两个受试者中是低的。一个受试者是一种非吸烟者的oATP2A1浓度,比下一个最近浓度高8.4倍,本身均高于任何其他转运蛋白的浓度。从基因表达和动物功能研究中已知oATP2A1,以存在于肺中。这些结果为肺中的异卵性置位提供了对肺炎的理解,并显示与其他组织相比的肺中运输蛋白的不同概况。 (c)2018年elestvier b.v.保留所有权利。

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