首页> 外文期刊>Journal of Agricultural and Food Chemistry >Differential protein expression of the inhibitory effects of a standardized extract from Scutellariae radix in liver cancer cell lines using liquid chromatography and tandem mass spectrometry
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Differential protein expression of the inhibitory effects of a standardized extract from Scutellariae radix in liver cancer cell lines using liquid chromatography and tandem mass spectrometry

机译:液相色谱和串联质谱法检测黄S标准提取物对肝癌细胞系的抑制作用的差异蛋白表达

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The purpose of this study is to verify the inhibitory effect of a chemically standardized extract from Scutellariae radix in liver cancer cell lines (HepG2). The botanical extract was prepared using pressurized liquid extraction (PLE). A method using proteolytic digest with single dimensional and two-dimensional liquid chromatography with tandem mass spectrometry was used to characterize differential protein expression in mammalian cells in response to the botanical extract. The whole cell lysates were digested with trypsin, and the peptides were separated by one-dimensional (reversed phase) or by two-dimensional (cation exchange and reversed phase) solid-phase extraction (SPE) cleanup and separated by liquid chromatography with UV detection and mass spectrometry. In the presence of the botanical extracts, drug-induced apoptosis was not observed, and a number of proteins that played an important role in the metabolic pathways in HepG2 cell line had been affected. The data, as presented, suggest that the inhibitory effects of the standardized extracts from Scutellariae radix resulted from expression of heat shock protein and other proteins related to energy metabolism. The proposed platform had the potential to provide significant information about the particular proteome such as human hepatoma HepG2. At the molecular level, it was possible to study the proteins and how their levels and modifications change in response to the effects of the botanical extract.
机译:这项研究的目的是验证黄S化学提取物在肝癌细胞系(HepG2)中的抑制作用。植物提取物是使用加压液体提取(PLE)制备的。一种使用蛋白水解消化液和一维和二维液相色谱串联质谱法的方法,用于表征响应植物提取物的哺乳动物细胞中蛋白质的差异表达。用胰蛋白酶消化全细胞裂解物,并通过一维(反相)或二维(阳离子交换和反相)固相萃取(SPE)净化分离肽,并通过液相色谱和紫外检测分离和质谱。在植物提取物的存在下,未观察到药物诱导的细胞凋亡,并且许多在HepG2细胞系的代谢途径中起重要作用的蛋白质也受到了影响。所提供的数据表明,黄cut标准提取物的抑制作用是由于热激蛋白和其他与能量代谢有关的蛋白的表达所致。拟议的平台具有提供有关特定蛋白质组(例如人肝癌HepG2)的重要信息的潜力。在分子水平上,有可能研究蛋白质以及它们的水平和修饰如何响应植物提取物的作用而变化。

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