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Differential liquid phase proteomic analysis of the effect of selenium supplementation in LNCaP cells

机译:补充LNCaP细胞中硒的影响的差分液相蛋白质组学分析

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The effect of 100 nM sodium selenite supplementation was studied on LNCaP cells by a proteomic approach, on ProteomeLab (TM) PF 2D platform. Proteins were separated by liquid phase bi-dimensional chromatography and analyzed by pair-wise alignment of peaks to detect those differentially expressed. Differential expression threshold was set at a twice difference level and proteins matching this criterion were identified by MALDI-TOF and confirmed by ESI-ion trap MS/MS. Not all differentially expressed proteins found by PF 2D could be identified by MS analysis, the sensitivity of which emerging as the limiting factor. Thus, only the most abundant proteins, differently expressed following selenium supplementation, were identified. We positively showed an increase of expression of thioredoxin reductase 1, enolase 1, phosphoglycerate mutase 1, glyceraldehyde3-phosphate dehydrogenase, heterogeneous nuclear ribonucleoprotein A2/B1, isoform A2, Ras-GTPase-activating protein SH3-domain-binding protein and Keratin 18 and a decrease of expression of peroxiredoxin I and heat shock protein 70, protein 8, isofonn 1. Results are consistent, at least in part, with the less oxidant environment brought about by the synthesis of Se-dependent peroxidases, keeping low the steady-state concentration of hydrogen peroxide. (c) 2008 Elsevier B.V. All rights reserved.
机译:在ProteomeLab(TM)PF 2D平台上,通过蛋白质组学方法研究了补充100 nM亚硒酸钠对LNCaP细胞的影响。通过液相二维色谱分离蛋白质,并通过峰的成对对齐分析以检测差异表达的峰。将差异表达阈值设置为两倍差异水平,并通过MALDI-TOF鉴定并通过ESI离子阱MS / MS确认符合此标准的蛋白质。并非所有通过PF 2D发现的差异表达蛋白质都可以通过MS分析来鉴定,其敏感性逐渐成为限制因素。因此,仅鉴定出最丰富的蛋白质,其在硒补充后以不同的方式表达。我们积极地显示了硫氧还蛋白还原酶1,烯醇酶1,磷酸甘油酸突变酶1,甘油醛3-磷酸脱氢酶,异质核糖核蛋白A2 / B1,同工型A2,Ras-GTPase激活蛋白SH3-结构域结合蛋白和角蛋白18和降低过氧化物酶I和热休克蛋白70,蛋白8,异黄酮1的表达。结果至少部分与Se依赖性过氧化物酶的合成所带来的较少的氧化环境一致,从而使稳态保持较低过氧化氢的浓度。 (c)2008 Elsevier B.V.保留所有权利。

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