SE157:/DS3
From Metabolonote
Sample Set Information
ID | TSE1313 |
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Title | Top-down Metabolomic Approaches for Nitrogen-Containing Metabolites. |
Description | Streamlining the processes that reveal heteroatom-containing metabolites and their biosynthetic genes is essential in integrated metabolomics studies. These metabolites are especially targeted for their potential pharmaceutical activities. By using a Fourier-transform ion cyclotron resonance-mass spectrometry (FTICR-MS) instrument, we provide top-down targeted metabolomic analyses using ultrahigh-resolution liquid chromatography-mass spectrometry (LC-MS), high-resolution matrix-assisted laser desorption/ionization (MALDI), and high-resolution imaging mass spectrometry (IMS) with 15N labeling of nitrogen-containing metabolites. In this study, we efficiently extract known and unknown chemicals and spatial information from the medicinal plant Catharanthus roseus, which sources several cancer drugs. The ultrahigh-resolution LC-MS analysis showed that the molecular formula of 65 N-metabolites were identified using the petals, peduncles, leaves, petioles, stems, and roots of the non- and 15N-labeled Catharanthus plants. The high resolution MALDI analysis showed the molecular formula of 64 N-metabolites using the petals, leaves, and stems of the non- and 15N-labeled Catharanthus. The chemical assignments using molecular formulas stored in databases identified known and unknown metabolites. The comparative analyses using the assigned metabolites revealed that most of the organ-specific ions are derived from unknown N-metabolites. The high-resolution IMS analysis characterized the spatial accumulation patterns of 32 N-metabolites using the buds, leaves, stems, and roots in Catharanthus. The comparative analysis using the non- and 15N-labeled IMS data showed the same spatial accumulation patterns of a non- and 15N-labeled metabolite in the organs, showing that top-down analysis can be performed even in IMS analysis. |
Authors | Nakabayashi R, Hashimoto K, Toyooka K, Saito K. |
Reference | Anal Chem. 2017 Mar 7;89(5):2698-2703. doi: 10.1021/acs.analchem.6b04163. Epub 2017 Feb 22. |
Comment |
Data Analysis Details Information
ID | DS3 |
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Title | Data Analysis (MALDI) |
Description | Elemental composition candidates were estimated in DataAnalysis under the following conditions: adduct type, [M + H]+; tolerance, 1 mDa; number of nitrogen atoms in formula, ≥1; charge, +1; check rings plus double bonds, ≤80; filter H/C ration, ≤3. Finally, the molecular formulas of the 64 N-ions were determined from the mass shifts of the target N-ions from the non-labeled data to the 15N-labeled data. To assign the molecular formulas, the metabolite information was extracted by searching the word “Catharanthus” in the databases KNApSAcK WEB: Keyword Search Web Version 1.000.01 and Dictionary of Natural Products 25.1. |
Comment_of_details |