首页> 外文期刊>Journal of proteome research >Untargeted Serum Metabolic Profiling by Comprehensive Two-Dimensional Gas Chromatography-High-Resolution Time-of-Flight Mass Spectrometry
【24h】

Untargeted Serum Metabolic Profiling by Comprehensive Two-Dimensional Gas Chromatography-High-Resolution Time-of-Flight Mass Spectrometry

机译:通过综合二维气相色谱 - 高分辨率飞行时间质谱法通过未确定的血清代谢分析

获取原文
获取原文并翻译 | 示例
       

摘要

While many laboratories take appropriate care, there are still cases where the performances of untargeted profiling methods suffer from a lack of design, control, and articulation of the various steps involved. This is particularly harmful to modern comprehensive analytical instrumentations that otherwise provide an unprecedented coverage of complex matrices. In this work, we present a global analytical workflow based on comprehensive two-dimensional gas chromatography coupled to high-resolution time-of-flight mass spectrometry. It was optimized for sample preparation and chromatographic separation and validated on in-house quality control (QC) and NIST SRM 1950 samples. It also includes a QC procedure, a multiapproach data (pre)processing workflow, and an original bias control procedure. Compounds of interest were identified using mass, retention, and biological information. As a proof of concept, 35 serum samples representing three subgroups of Crohn's disease (with high, low, and quiescent endoscopic activity) were analyzed along with 33 healthy controls. This led to the selection of 33 unique candidate biomarkers able to classify the Crohn's disease and healthy samples with an orthogonal partial least-squares discriminant analysis Q(2) of 0.48 and a receiver-operating-characteristic area under the curve of 0.85 (100% sensitivity and 82% specificity in cross validation). Fifteen of these 33 candidates were reliably annotated (Metabolomics Standards Initiative level 2).
机译:虽然许多实验室采取适当的护理,但仍有案例仍然存在未明确的分析方法的表现遭受缺乏的设计,控制和涉及的各种步骤的关节。这对现代综合分析仪器特别有害,否则提供了复杂矩阵的前所未有的覆盖范围。在这项工作中,我们基于综合二维气相色谱耦合到高分辨率飞行时间质谱法的全局分析工作流程。它针对样品制备和色谱分离进行了优化,并在内部质量控制(QC)和NIST SRM 1950样品上验证。它还包括QC过程,多APProach数据(Pre)处理工作流程以及原始偏置控制过程。使用质量,保留和生物学信息来鉴定目的化合物。作为概念证明,分析了35种表示克罗恩病(高,低,静态的内窥镜活性)的三个亚组的血清样本以及33例健康对照。这导致了选择33个独特的候选生物标志物,能够将克罗恩病和健康样品分类,具有0.48的正交部分最小二乘判别Q(2)和0.85曲线下的接收器操作特征区域(100%交叉验证的敏感性和82%的特异性)。这33个候选物中的十五个是可靠的注释(代谢组学标准倡议2级)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号