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人类脑脊液个体内和个体间变异的比较蛋白质组学分析

Comparative proteomic analysis of intra- and interindividual variation in human cerebrospinal fluid.

作者信息

Hu Yan, Malone James P, Fagan Anne M, Townsend R Reid, Holtzman David M

机构信息

Department of Neurology, Division of Metabolism and Proteomics Center, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Mol Cell Proteomics. 2005 Dec;4(12):2000-9. doi: 10.1074/mcp.M500207-MCP200. Epub 2005 Sep 30.

Abstract

Cerebrospinal fluid (CSF) is a potential source of biomarkers for many disorders of the central nervous system, including Alzheimer disease (AD). Prior to comparing CSF samples between individuals to identify patterns of disease-associated proteins, it is important to examine variation within individuals over a short period of time so that one can better interpret potential changes in CSF between individuals as well as changes within a given individual over a longer time span. In this study, we analyzed 12 CSF samples, composed of pairs of samples from six individuals, obtained 2 weeks apart. Multiaffinity depletion, two-dimensional DIGE, and tandem mass spectrometry were used. A number of proteins whose abundance varied between the two time points was identified for each individual. Some of these proteins were commonly identified in multiple individuals. More importantly, despite the intraindividual variations, hierarchical clustering and multidimensional scaling analysis of the proteomic profiles revealed that two CSF samples from the same individual cluster the closest together and that the between-subject variability is much larger than the within-subject variability. Among the six subjects, comparison between the four cognitively normal and the two very mildly demented subjects also yielded some proteins that have been identified in previous AD biomarker studies. These results validate our method of identifying differences in proteomic profiles of CSF samples and have important implications for the design of CSF biomarker studies for AD and other central nervous system disorders.

摘要

脑脊液(CSF)是包括阿尔茨海默病(AD)在内的许多中枢神经系统疾病生物标志物的潜在来源。在比较个体之间的脑脊液样本以识别疾病相关蛋白质模式之前,重要的是检查个体在短时间内的变化,以便更好地解释个体之间脑脊液的潜在变化以及给定个体在较长时间内的变化。在本研究中,我们分析了12份脑脊液样本,这些样本由来自6个人的成对样本组成,样本采集间隔为2周。使用了多亲和去除、二维差异凝胶电泳和串联质谱分析。为每个个体鉴定出了一些在两个时间点之间丰度不同的蛋白质。其中一些蛋白质在多个个体中被共同鉴定出来。更重要的是,尽管存在个体内差异,但蛋白质组学图谱的层次聚类和多维尺度分析表明,来自同一个体的两份脑脊液样本聚类最紧密,且个体间变异性远大于个体内变异性。在这6名受试者中,对4名认知正常者和2名极轻度痴呆者进行比较,也发现了一些在先前AD生物标志物研究中已鉴定出的蛋白质。这些结果验证了我们识别脑脊液样本蛋白质组学图谱差异的方法,对AD和其他中枢神经系统疾病脑脊液生物标志物研究的设计具有重要意义。

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