Summary of Study ST003808

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 PR002382. The data can be accessed directly via it's Project DOI: 10.21228/M8QZ7Q 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 IDST003808
Study TitleGlucose-6-phosphate-dehydrogenase on old peroxisomes maintains self-renewal of epithelial stem cells after asymmetric cell division
Study SummaryPeroxisomes play a crucial role in cellular metabolism. Glucose-6-phosphate dehydrogenase (G6PD), the gatekeeper enzyme of the pentose phosphate pathway, is primarily localized in the cytosol. However, studies have reported its presence in peroxisomes as well. This project aims to determine the function of G6PD on the peroxisomal membrane. In this study, we overexpressed G6PD in either the cytosol or on the peroxisomal membrane of mammary epithelial stem-like cells (hMECs). By comparing their lipidomic profiles, we found that peroxisomal membrane-associated G6PD provides NADPH, which feeds into peroxisomal ether lipid synthesis.
Institute
University of Helsinki
DepartmentFaculty of Biological and Environmental Sciences
LaboratoryKatajisto Laboratory
Last NameHien
First NameBui
AddressBiocenter 1, Viikinkaari 9
Emailhien.bui@helsinki.fi
Phone+358294159407
Submit Date2025-03-06
Raw Data AvailableYes
Raw Data File Type(s)cdf, mzdata.xml
Analysis Type DetailGC-MS/LC-MS
Release Date2025-03-24
Release Version1
Bui Hien Bui Hien
https://dx.doi.org/10.21228/M8QZ7Q
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN006261 AN006262
Chromatography ID CH004749 CH004750
MS ID MS005963 MS005964
Analysis type MS MS
Chromatography type GC Reversed phase
Chromatography system Shimadzu GC-2010 Agilent 1290 Infinity
Column Phenomenex Zebron ZB-wax capillary (30m x 0.25mm, 0.25um) Phenomenex Luna Omega C18 (50 x 2.1mm, 1.6um, 100 Å)
MS Type EI ESI
MS instrument type GC-FID & GC-MSD Triple quadrupole
MS instrument name Shimadzu QP2010 Plus Agilent 6490 QQQ
Ion Mode POSITIVE NEGATIVE
Units pmol/sample peak area

Chromatography:

Chromatography ID:CH004749
Chromatography Summary:The samples were injected into a GC-2010 Plus gas chromatograph (Shimadzu Scientific Instruments, Kyoto, Japan) with flame-ionization detector (FID) for quantification of the analytes. Both GC systems were equipped with Zebron ZB-wax capillary columns (30 m, 0.25 mm ID and film thickness 0.25 μm; Phenomenex, Torrence CA, USA). GC-FID chromatographic peak areas (in the TXT files; analyte retention times in Table 1) were converted to mol% using the theoretical correction factors for FID (6), and the FOHs were calculated as µmol/10^6 cells.
Instrument Name:Shimadzu GC-2010
Column Name:Phenomenex Zebron ZB-wax capillary (30m x 0.25mm, 0.25um)
Column Temperature:280 °C for FID and 210 °C for MSD.
Flow Gradient:NA
Flow Rate:1.8 ml min–1 for FID and 1.0 ml min–1 for MSD
Solvent A:NA
Solvent B:NA
Chromatography Type:GC
  
Chromatography ID:CH004750
Chromatography Summary:The method used acetonitrile/water/isopropanol-based solvent system, Agilent 1290 Infinity HPLC (Agilent Technologies, Santa Clara, CA) equipped with a Luna Omega C18 100 Å (50 x 2.1 mm, 1.6 μm) column (Phenomenex) and Agilent 6490 Triple Quad LC/MS with iFunnel Technology. The lipids species were identified and quantified using lipid class-specific precursor ion and neutral loss detection modes. PE plasmalogens (PE P) were identified with alkenyl chain (16:0, 18:0, 18:1)-specific scans and quantified from MS- scan. - Due to a contamination during the sample run, some samples were removed from analysis
Instrument Name:Agilent 1290 Infinity
Column Name:Phenomenex Luna Omega C18 (50 x 2.1mm, 1.6um, 100 Å)
Column Temperature:25
Flow Gradient:32% B at 0.0 min, 32% B at 1.5 min, 45% B at 4.0 min, 52% B at 5.0 min, 58% B at 8.0 min, 66% B at 11.0 min, 70% B at 14.0 min, 75% B at 18.0 min, 97% B at 21.0 min, 97% B at 25.0 min, 32% B at 26.0 min, 32% B at 32.0 min. flow gradient field is a linear gradient
Flow Rate:0.200 mL/min
Solvent A:40% water/60% acetonitrile; 0.1% formic acid; 10mM ammonium formate
Solvent B:90% isopropanol/10% acetonitrile; 0.1% formic acid; 10mM ammonium formate
Chromatography Type:Reversed phase
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