Institute of Medicine, University of Bergen, Bergen, Norway.
Proteomics Clin Appl. 2007 Jul;1(7):699-711. doi: 10.1002/prca.200700126.
Cerebrospinal fluid (CSF) is a perfect source to search for new biomarkers to improve early diagnosis of neurological diseases. Standardization of pre-analytical handling of the sample is, however, important to obtain acceptable analytical quality. In the present study, MALDI-TOF MS was used to examine the influence of pre-analytical sample procedures on the low molecular weight (MW) CSF proteome. Different storage conditions like temperature and duration or the addition of as little as 0.2 µL blood/mL neat CSF caused significant changes in the mass spectra. The performance of different types of MW cut-off spin cartridges from different suppliers used to enrich the low MW CSF proteome showed great variance in cut-off accuracy, stability and reproducibility. The described analytical method achieved a polypeptide discriminating limit of approximately 800 pM, two to three orders of magnitude lower than reported for plasma. Based on this study, we recommend that CSF is centrifuged immediately after sampling, prior to storage at -80ºC without addition of protease inhibitors. Guanidinium hydrochloride is preferred to break protein-protein interactions. A spin cartridge with cut-off limit above the intended analytical mass range is recommended. Our study contributes to the important task of developing standardized pre-analytical protocols for the proteomic study of CSF.
脑脊液(CSF)是寻找新生物标志物以改善神经疾病早期诊断的理想来源。然而,为了获得可接受的分析质量,对样本的分析前处理进行标准化非常重要。在本研究中,MALDI-TOF MS 被用于研究分析前样本处理对低分子量(MW)CSF 蛋白质组的影响。不同的储存条件,如温度和持续时间,或仅向未稀释的 CSF 中添加 0.2 μL 血液,都会导致质谱出现显著变化。用于富集低 MW CSF 蛋白质组的不同供应商的不同类型的 MW 截止值 spin 试剂盒的性能在截止值准确性、稳定性和重现性方面存在很大差异。所描述的分析方法实现了约 800 pM 的多肽区分限,比报道的血浆低两个到三个数量级。基于这项研究,我们建议在将 CSF 储存于-80°C 之前,应立即在采样后离心,而无需添加蛋白酶抑制剂。盐酸胍优先用于破坏蛋白质-蛋白质相互作用。建议使用截止值限制在预期分析质量范围内的 spin 试剂盒。我们的研究有助于为 CSF 的蛋白质组学研究制定标准化分析前方案这一重要任务。