Qin Zhaoyu, Qin Yanjiang, Liu Shilian
Biology Science Department, Marine College, Shandong University at Weihai, Weihai, Shandong 264209, People's Republic of China.
Cell Mol Neurobiol. 2009 Mar;29(2):203-10. doi: 10.1007/s10571-008-9312-z. Epub 2008 Sep 19.
The diagnosis of multiple sclerosis (MS) is still challenging recently due to the lack of a specific diagnostic test. Proteomics analysis was applied to biomarkers discovery and their pathways study.
First, the proteins of CSF from MS patients and control group were analyzed individually with 2D-DIGE technology (two-dimensional difference gel electrophoresis). Then, protein spots were found out with DeCyder6.0 software which showed different expression levels in the gel images between the two groups. The information regarding these proteins was collected based on MALDI-TOF/MS and related database searches. Lastly, interaction between these proteins was further analyzed by using Metacore software.
There were 13 proteins that showed more than 1.5-fold difference in expression levels between the two groups. Furthermore, the identification made by MALDI-TOF/MS revealed that one of the most significant differential proteins was DBP (vitamin D-binding protein), which decreased in the experimental group. This result was confirmed by ELISA (P < 0.01). Moreover, network between the 13 proteins were partially got, which showed some biological interactions.
These results support a correlation between the level of DBP and MS. DBP may be a potential useful biomarker for diagnosis or a medicine target for treatment of MS.
由于缺乏特异性诊断测试,目前多发性硬化症(MS)的诊断仍具有挑战性。蛋白质组学分析被应用于生物标志物的发现及其通路研究。
首先,采用二维差异凝胶电泳(2D-DIGE)技术分别分析MS患者和对照组脑脊液中的蛋白质。然后,使用DeCyder6.0软件找出两组凝胶图像中表达水平不同的蛋白质斑点。基于基质辅助激光解吸电离飞行时间质谱(MALDI-TOF/MS)和相关数据库搜索收集这些蛋白质的信息。最后,使用Metacore软件进一步分析这些蛋白质之间的相互作用。
两组之间有13种蛋白质的表达水平差异超过1.5倍。此外,MALDI-TOF/MS鉴定显示,最显著的差异蛋白之一是DBP(维生素D结合蛋白),其在实验组中减少。酶联免疫吸附测定(ELISA)证实了这一结果(P < 0.01)。此外,部分获得了这13种蛋白质之间的网络,显示出一些生物学相互作用。
这些结果支持DBP水平与MS之间的相关性。DBP可能是MS诊断的潜在有用生物标志物或治疗的药物靶点。