Davidsson Pia, Sjögren Magnus
Discovery Medicine/Molecular Pharmacology, AstraZeneca R&D, Mölndal, SE-431 83 Mölndal, Sweden.
Mech Ageing Dev. 2006 Feb;127(2):133-7. doi: 10.1016/j.mad.2005.09.021. Epub 2005 Nov 15.
Proteins in cerebrospinal fluid (CSF) may often serve as indicators of neurodegenerative diseases, and are a rich source for biomarker discovery. However, a large dynamic range of proteins in CSF makes the analysis very challenging because high abundant proteins tend to mask those of lower abundance. Therefore, advances in the proteomic analysis had to be applied in the screen for new specific biomarkers for Alzheimer's disease (AD). In this study, we have summarised the studies regarding two-dimensional gel electrophoresis (2-DE), and surface enhanced laser desorption/ionisation mass spectrometry (SELDI) technology that have been used in CSF of AD patients. Many proteins have shown to be altered in CSF of AD patients compared to controls, by using a protein pattern, from 2-D gel analysis or from SELDI analysis. Several studies show that the use of a panel of biomarkers derived from proteomic analysis is an advantageous way to distinguish AD from normal, and other dementia subjects.
脑脊液(CSF)中的蛋白质常常可作为神经退行性疾病的指标,并且是生物标志物发现的丰富来源。然而,脑脊液中蛋白质的动态范围很大,这使得分析极具挑战性,因为高丰度蛋白质往往会掩盖低丰度蛋白质。因此,蛋白质组学分析的进展必须应用于阿尔茨海默病(AD)新的特异性生物标志物的筛选。在本研究中,我们总结了关于二维凝胶电泳(2-DE)和表面增强激光解吸/电离质谱(SELDI)技术的研究,这些技术已用于AD患者的脑脊液分析。通过二维凝胶分析或SELDI分析得到的蛋白质图谱显示,与对照组相比,AD患者脑脊液中的许多蛋白质发生了改变。多项研究表明,使用一组源自蛋白质组学分析的生物标志物是区分AD与正常人和其他痴呆患者的一种有利方法。