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使用带有内标的同位素残基异常值分析(IROA)的定量代谢组学

Quantitative Metabolomics Using Isotope Residue Outlier Analysis (IROA) with Internal Standards.

作者信息

Mendez Roberto, Del Carmen Piqueras Maria, Raskind Alexander, de Jong Felice A, Beecher Chris, Bhattacharya Sanjoy K, Banerjee Santanu

机构信息

Department of Surgery, Miller School of Medicine, University of Miami, Miami, FL, USA.

Bascon Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, USA.

出版信息

Methods Mol Biol. 2019;1996:41-46. doi: 10.1007/978-1-4939-9488-5_4.

Abstract

Various research strategies involving biomarker discovery and mechanistic studies in system biology depend on reproducible and reliable quantification of all metabolites from tissue(s) of interest. Contemporary analytical methods rely on mass spectrometry-based targeted and/or untargeted metabolomics platforms. The robustness of these analyses depends on the cleanliness of the samples, accuracy of the database, resolution of the instrument, and, the most variable of the list, the personal preferences of the researcher and the instrument operator. In this chapter, we introduce a simple method to prepare murine liver samples and carry it through the Isotope Ratio Outlier Analysis (IROA) pipeline. This pipeline encompasses sample preparation, LC-MS-based peak acquisition, proprietary software-based library creation, normalization, and quantification of metabolites. IROA offers a unique platform to create and normalize a local library and account for run-to-run variability over years of acquisition using the internal standards (IROA-IS) and long-term reference standards (IROA-LTRS).

摘要

系统生物学中涉及生物标志物发现和机制研究的各种研究策略,都依赖于对来自感兴趣组织的所有代谢物进行可重复且可靠的定量分析。当代分析方法依赖于基于质谱的靶向和/或非靶向代谢组学平台。这些分析的稳健性取决于样品的纯净度、数据库的准确性、仪器的分辨率,以及(列表中最具变数的)研究人员和仪器操作员的个人偏好。在本章中,我们介绍一种制备小鼠肝脏样品并将其通过同位素比率异常值分析(IROA)流程的简单方法。该流程包括样品制备、基于液相色谱-质谱的峰采集、基于专有软件的库创建、归一化以及代谢物定量。IROA提供了一个独特的平台,用于创建和归一化本地库,并使用内标(IROA-IS)和长期参考标准(IROA-LTRS)来解释多年采集过程中的批次间差异。

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