Summary of Study ST002375

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 PR001528. The data can be accessed directly via it's Project DOI: 10.21228/M8612V This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

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.

Perform statistical analysis  |  Show all samples  |  Show named metabolites  |  Download named metabolite data  
Download mwTab file (text)   |  Download mwTab file(JSON)   |  Download data files (Contains raw data)
Study IDST002375
Study TitleMetabolomics analysis of WT or GOT1 knockout CD8+ T cells cultured in serine-replete or serine-free media
Study SummaryWT or GOT1 knockout CD8+ T cells were activated with plate-bound anti-CD3 or soluble anti-CD28, in serine-replete or serine-free media for 24 hours. Intracellular metabolome were assessed by MS.
Institute
Johns Hopkins University
Last NameXu
First NameWei
Address1650 Orleans Street, Baltimore, MD 21287, USA.
Emailwxu29@jhmi.edu
Phone443-220-9936
Submit Date2022-11-30
Raw Data AvailableYes
Raw Data File Type(s)wiff
Analysis Type DetailLC-MS
Release Date2023-11-28
Release Version1
Wei Xu Wei Xu
https://dx.doi.org/10.21228/M8612V
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

Select appropriate tab below to view additional metadata details:


Project:

Project ID:PR001528
Project DOI:doi: 10.21228/M8612V
Project Title:Metabolomics analysis of WT or GOT1 knockout CD8+ T cells cultured in serine-replete or serine-free media
Project Summary:WT or GOT1 knockout CD8+ T cells were activated with plate-bound anti-CD3 or soluble anti-CD28, in serine-replete or serine-free media for 24 hours. Intracellular metabolome were assessed by MS.
Institute:Johns Hopkins University
Last Name:Xu
First Name:Wei
Address:1650 Orleans Street, Baltimore, MD 21287, USA.
Email:wxu29@jhmi.edu
Phone:443-220-9936

Subject:

Subject ID:SU002464
Subject Type:Cultured cells
Subject Species:Mus musculus
Taxonomy ID:10090
Species Group:Mammals

Factors:

Subject type: Cultured cells; Subject species: Mus musculus (Factor headings shown in green)

mb_sample_id local_sample_id Treatment
SA237363sample 6GOT1 KO_Serine-free
SA237364sample 4GOT1 KO_Serine-free
SA237365sample 5GOT1 KO_Serine-free
SA237366sample 11GOT1 KO_Serine-replete
SA237367sample 10GOT1 KO_Serine-replete
SA237368sample 12GOT1 KO_Serine-replete
SA237369sample 1WT_Serine-free
SA237370sample 3WT_Serine-free
SA237371sample 2WT_Serine-free
SA237372sample 7WT_Serine-replete
SA237373sample 8WT_Serine-replete
SA237374sample 9WT_Serine-replete
Showing results 1 to 12 of 12

Collection:

Collection ID:CO002457
Collection Summary:Cell pellets were spun down and washed twice with pre-warmed PBS. Metabolites were immediately extracted or stored at -80℃ until further extraction.
Sample Type:Cultured cells

Treatment:

Treatment ID:TR002476
Treatment Summary:CD8+ T cells were isolated from spleens and lymph nodes of WT or T cell conditional GOT1 knockout mice. Cells were then activated with plate-bound anti-CD3 and soluble anti-CD28 for 24 hours in normal media (serine-replete) or serine-free media.

Sample Preparation:

Sampleprep ID:SP002470
Sampleprep Summary:Cell pellets were spun down and washed twice with pre-warmed PBS. Metabolites were immediately extracted by adding methanol:water (80:20, v/v) extraction solution, sonicated and stored at -80 °C for at least 2 hours to precipitate the proteins. Supernatant after centrifugation at 14,000xg for 10 minutes was dried under nitrogen gas. Metabolites were then reconstituted using ACN:water (50:50, v/v) overnight at 4 °C. Soluble metabolites after centrifugation at 14,000xg for 10 minutes were subjected to targeted metabolite analysis by liquid-chromatography tandem mass spectrometry (LC-MS/MS).

Chromatography:

Chromatography ID:CH002868
Instrument Name:Shimadzu Prominence UFLC
Column Name:Waters XBridge BEH Amide XP HILIC (150 x 2.1mm,2.5um)
Chromatography Type:HILIC

Analysis:

Analysis ID:AN003870
Analysis Type:MS
Chromatography ID:CH002868
Num Factors:4
Num Metabolites:147
Units:AUC
  logo