Department of Biochemistry, Purdue University, West Lafayette, IN, United States; Purdue Center for Plant Biology, Purdue University, West Lafayette, IN, United States.
Department of Biochemistry, Purdue University, West Lafayette, IN, United States; Purdue Center for Plant Biology, Purdue University, West Lafayette, IN, United States.
Methods Enzymol. 2022;676:279-303. doi: 10.1016/bs.mie.2022.07.039. Epub 2022 Sep 22.
Untargeted liquid chromatography/mass spectrometry (LC-MS) can contribute a comprehensive and unbiased picture of the metabolic space of plants. These data can be used to quantify natural metabolite variation for genome wide association studies, to compare global metabolic responses from environmental or genetic perturbations, and to identify previously undescribed metabolites in Nature. A major limitation with untargeted metabolomics is the classification and identification of the thousands of metabolite features that can be detected in a single analytical run. Isotopic labeling improves the informational value of these datasets by categorizing metabolites as being derived from specific upstream precursors and/or to known metabolic pathways. When a C-labeled precursor is fed to either a plant or tissue, the downstream metabolites produced from it have a higher m/z value than the molecules in the pre-existing pool, generating an m/z peak pair that can be specifically identified within the MS data. This paper outlines methods and principles to consider when supplementing untargeted MS data with isotopic labeling, including how to choose the appropriate isotopic label, grow and feed plant tissues to maximize label uptake and incorporation into derivatives, optimize LC-MS methods, and interpret the resulting labeling data. Although the focus here is on annotation of amino acid-derived metabolites using LC-MS, we anticipate that the methods are generally adaptable to other precursors, plant species, and chromatographic approaches.
非靶向液相色谱/质谱(LC-MS)可以提供植物代谢空间的全面、无偏的图谱。这些数据可用于对全基因组关联研究中的天然代谢物变异进行定量,比较环境或遗传扰动引起的全局代谢反应,并鉴定自然界中以前未描述的代谢物。非靶向代谢组学的一个主要限制是对数千种在单个分析运行中可检测到的代谢物特征进行分类和鉴定。同位素标记通过将代谢物分类为源自特定上游前体和/或已知代谢途径,提高了这些数据集的信息价值。当向植物或组织中添加 C 标记的前体时,由其产生的下游代谢物的 m/z 值比现有池中的分子高,从而在 MS 数据中生成可特异性识别的 m/z 峰对。本文概述了在用同位素标记补充非靶向 MS 数据时需要考虑的方法和原则,包括如何选择合适的同位素标记物、如何种植和喂养植物组织以最大程度地提高标记物的摄取和转化为衍生物、优化 LC-MS 方法以及解释所得标记数据。虽然这里的重点是使用 LC-MS 注释氨基酸衍生代谢物,但我们预计这些方法通常适用于其他前体、植物物种和色谱方法。