Summary of Study ST002778

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001733. The data can be accessed directly via it's Project DOI: 10.21228/M8PX3J This work is supported by NIH grant, U2C- DK119886.

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This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002778
Study TitleCell Lineage-Guided Microanalytical Mass Spectrometry Reveals Increased Energy Metabolism and Reactive Oxygen Species in the Vertebrate Organizer
Study SummaryWe performed targeted metabolomic analysis on the Spemann-Mangold Organizer (SMO) tissue in the frog (Xenopus laevis) and the remainder of dissected embryos (RE). Metabolites were extracted from the dissected tissues, reconstituted, and analyzed using liquid chromatography (LC) electrospray ionization (ESI) mass spectrometry (MS). The targeted metabolite measurements were performed on a trapped ion mobility time-of-flight mass spectrometer (timsTOF PRO, Bruker).
Institute
University of Maryland
DepartmentChemistry & Biochemistry
Last NameNemes
First NamePeter
Address8051 Regents Drive, College Park, MD 20742, USA
Emailnemes@umd.edu
Phone3014050373
Submit Date2023-07-03
Raw Data AvailableYes
Raw Data File Type(s)d
Analysis Type DetailLC-MS
Release Date2024-01-10
Release Version1
Peter Nemes Peter Nemes
https://dx.doi.org/10.21228/M8PX3J
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001733
Project DOI:doi: 10.21228/M8PX3J
Project Title:Cell Lineage-Guided Microanalytical Mass Spectrometry Reveals Increased Energy Metabolism and Reactive Oxygen Species in the Vertebrate Organizer
Project Summary:We performed targeted metabolomic analysis on the Spemann-Mangold Organizer (SMO) tissue in the frog (Xenopus laevis) and the remainder of dissected embryos (RE). The goal of this study is to quantify a panel of targeted metabolite intermediates from glycolysis, phosphate energy pool, and mitochondrial activity including the TCA cycle. Metabolites were extracted from the dissected tissues, reconstituted, and analyzed using liquid chromatography (LC) electrospray ionization (ESI) mass spectrometry (MS). The targeted metabolite measurements were performed on a trapped ion mobility time-of-flight mass spectrometer (timsTOF PRO, Bruker). Targeted MS assays on the metabolite intermediates produced downstream, complemented by classical fluorescence-based metabolite assays when available, revealed local oxidative stress and enrichment of reactive oxygen species (ROS) in the SMO.
Institute:University of Maryland
Department:Chemistry & Biochemistry
Last Name:Nemes
First Name:Peter
Address:8051 Regents Drive, College Park, MD 20742, USA
Email:nemes@umd.edu
Phone:301-405-0373
Funding Source:National Institutes of Health under Award no. 1R35GM124755
Contributors:Aparna B. Baxi, Jie Li, Vi M. Quach, and Peter Nemes
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