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采用 iTRAQ 和 SID-SRM 技术发现并初步验证多发性硬化症患者和对照者之间差异丰度蛋白。

Discovery and initial verification of differentially abundant proteins between multiple sclerosis patients and controls using iTRAQ and SID-SRM.

机构信息

Proteomics Unit (PROBE), Department of Biomedicine, University of Bergen, Bergen, Norway.

出版信息

J Proteomics. 2013 Jan 14;78:312-25. doi: 10.1016/j.jprot.2012.09.037. Epub 2012 Oct 8.

Abstract

In the present study, we aimed to discover cerebrospinal fluid (CSF) proteins with significant abundance difference between early multiple sclerosis patients and controls, and do an initial verification of these proteins using selected reaction monitoring (SRM). iTRAQ and Orbitrap MS were used to compare the CSF proteome of patients with clinically isolated syndrome (CIS) (n=5), patients with relapsing-remitting multiple sclerosis that had CIS at the time of lumbar puncture (n=5), and controls with other inflammatory neurological disease (n=5). Of more than 1200 identified proteins, five proteins were identified with significant abundance difference between the patients and controls. In the initial verification using SRM we analyzed a larger patient and control cohort (n=132) and also included proteins reported as differentially abundant in multiple sclerosis in the literature. We found significant abundance difference for 11 proteins after verification, of which the five proteins alpha-1-antichymotrypsin, contactin-1, apolipoprotein D, clusterin, and kallikrein-6 were significantly differentially abundant in several of the group comparisons. This initial study form the basis for further biomarker verification studies in even larger sample cohorts, to determine if these proteins have relevance as diagnostic or prognostic biomarkers for multiple sclerosis.

摘要

在本研究中,我们旨在发现早发性多发性硬化症患者和对照组之间脑脊液(CSF)中具有显著丰度差异的蛋白质,并使用选择反应监测(SRM)对这些蛋白质进行初步验证。iTRAQ 和 Orbitrap MS 用于比较临床孤立综合征(CIS)患者(n=5)、腰椎穿刺时患有复发缓解型多发性硬化症且具有 CIS 的患者(n=5)和具有其他炎症性神经疾病的对照组(n=5)的 CSF 蛋白质组。在超过 1200 种鉴定的蛋白质中,有 5 种蛋白质在患者和对照组之间存在显著的丰度差异。在使用 SRM 进行的初步验证中,我们分析了更大的患者和对照组队列(n=132),并包括了文献中报道的多发性硬化症中差异丰度的蛋白质。经过验证后,我们发现 11 种蛋白质的丰度存在显著差异,其中 alpha-1-抗胰凝乳蛋白酶、接触蛋白-1、载脂蛋白 D、簇蛋白和激肽释放酶-6 在几个组比较中差异显著。这项初步研究为在更大的样本队列中进一步进行生物标志物验证研究奠定了基础,以确定这些蛋白质是否作为多发性硬化症的诊断或预后生物标志物具有相关性。

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