Auer Michael, Hegen Harald, Rudzki Dagmar, Golderer Georg, Deisenhammer Florian
Department of Neurology, Medical University of Innsbruck, Innrain 66, 6020 Innsbruck, Austria.
Division of Biological Chemistry, Medical University of Innsbruck, Innrain 80-83, 6020 Innsbruck, Austria.
Diagnostics (Basel). 2018 Jul 5;8(3):44. doi: 10.3390/diagnostics8030044.
Two-dimensional difference gel electrophoresis (2D-DIGE) has been used for identification of possible biomarkers in the cerebrospinal fluid (CSF) of multiple sclerosis (MS) patients. However, in different studies inconsistent results have been obtained. We wanted to analyze the diagnostic value of 2D-DIGE in early MS patients by comparing protein patterns between single and pooled samples of MS patients and controls. CSF samples of 20 MS patients and 10 control subjects were processed with 2D-DIGE. The so obtained protein patterns were analyzed with DeCyder 6.5 software, whereby we described variation of patterns presented in one gel as well as between different gels. Even when running single samples of patients of the same group in one gel, variation of protein patterns was high. The number of identified spots with different protein level varied between 4 and 30, depending on which sample batches were compared. We did not find a consistent pattern throughout all possible batch combinations. The inter-individual variation of protein expression as well as the susceptibility of 2D-DIGE for methodological variations makes use of 2D-DIGE as a diagnostic tool for MS and for detection of possible candidate biomarkers difficult, since detected proteins vary depending on which samples are compared.
二维差异凝胶电泳(2D-DIGE)已被用于鉴定多发性硬化症(MS)患者脑脊液(CSF)中可能的生物标志物。然而,在不同的研究中得到了不一致的结果。我们希望通过比较MS患者和对照的单个样本与混合样本之间的蛋白质模式,分析2D-DIGE在早期MS患者中的诊断价值。对20例MS患者和10例对照受试者的脑脊液样本进行2D-DIGE处理。用DeCyder 6.5软件分析所得的蛋白质模式,从而描述了在一块凝胶中以及不同凝胶之间呈现的模式变化。即使在一块凝胶中运行同一组患者的单个样本时,蛋白质模式的变化也很大。根据所比较的样本批次不同,鉴定出的具有不同蛋白质水平的斑点数量在4到30之间变化。在所有可能的批次组合中,我们都没有发现一致的模式。蛋白质表达的个体间差异以及2D-DIGE对方法学变化的敏感性使得将2D-DIGE用作MS的诊断工具以及检测可能的候选生物标志物变得困难,因为检测到的蛋白质会因所比较的样本不同而有所变化。