Summary of Study ST003121

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 PR001939. The data can be accessed directly via it's Project DOI: 10.21228/M8343B 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.

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Study IDST003121
Study TitleMetabolomic profiling of ALG13-CDG brain organoids
Study SummaryALG13-CDG is a rare inborn error of metabolism caused by deficiency of the ALG13 enzyme, which is believed to lead to impaired protein glycosylation. While the disorder has primarily neurological presentation, there is limited knowledge about the specific brain-related changes that result from ALG13 deficiency. We used 3D brain organoids derived from fibroblasts of the individuals with ALG13-CDG to probe the brain-specific metabolic changes in ALG13-CDG.
Institute
Mayo Clinic
Last NameRadenkovic
First NameSilvia
Address200 2nd Ave SW Rochester MN, USA
Emailsilradenkovic@gmail.com
Phone507(77) 6-6107
Submit Date2024-03-06
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2025-03-06
Release Version1
Silvia Radenkovic Silvia Radenkovic
https://dx.doi.org/10.21228/M8343B
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001939
Project DOI:doi: 10.21228/M8343B
Project Title:Metabolomic profiling of ALG13-CDG brain organoids
Project Summary:ALG13-CDG is a rare inborn error of metabolism caused by deficiency of the ALG13 enzyme, which is believed to lead to impaired protein glycosylation. While the disorder has primarily neurological presentation, there is limited knowledge about the specific brain-related changes that result from ALG13 deficiency. We used 3D brain organoids derived from fibroblasts of the individuals with ALG13-CDG to probe the brain-specific metabolic changes in ALG13-CDG.
Institute:Mayo Clinic
Last Name:Radenkovic
First Name:Silvia
Address:200 2nd Ave SW Rochester MN
Email:silradenkovic@gmail.com
Phone:507(77) 6-6107
Funding Source:NIH

Subject:

Subject ID:SU003238
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Genotype Strain:WT/ALG13-CDG
Age Or Age Range:5-25
Gender:Male and female
Species Group:Mammals

Factors:

Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Genotype Sample source
SA338109SR01ALG13 Brain organoids
SA338110SR03ALG13 Brain organoids
SA338111SR02ALG13 Brain organoids
SA338112SR06CTR Brain organoids
SA338113SR04CTR Brain organoids
SA338114SR05CTR Brain organoids
Showing results 1 to 6 of 6

Collection:

Collection ID:CO003231
Collection Summary:Brain were collected at day in vitro 77.
Sample Type:Brain organoids
Storage Conditions:-80℃

Treatment:

Treatment ID:TR003247
Treatment Summary:NA

Sample Preparation:

Sampleprep ID:SP003245
Sampleprep Summary:Briefly, 4-5 organoids per cell line were collected and washed three times in PBS. The PBS was then removed, the organoids flash frozen and kept in -80 °C prior to metabolomics experiments. The metabolites were extracted using two phase extraction protocol. First, the organoids were transferred to lysing matrix tube and 350 µL of ice-cold extraction buffer (80 % MeOH, IS) was added to the sample. Next, the organoids were lyzed with ribolyzer, the lysate transferred to 1.5 mL Eppendorf tube and placed overnight at -80 °C. Further, the samples were centrifuged at 15,000 rpm, 4 °C, 20 min. 100 µL of supernatant was transferred to a fresh Eppendorf tube and 35 µL of ddH20 was added, followed by 800 µL 100% chloroform. The samples were then vortexed and stored at 4 °C overnight. Next, the polar phase was then used for Liquid Chromatography/Mass Spectrometry (LC/MS).
Processing Storage Conditions:-80℃
Extract Storage:-80℃

Combined analysis:

Analysis ID AN005115
Analysis type MS
Chromatography type Reversed phase
Chromatography system Waters Acquity
Column Waters ACQUITY UPLC HSS T3 (150 x 2.1mm,1.8um)
MS Type ESI
MS instrument type Orbitrap
MS instrument name Thermo Q Exactive Orbitrap
Ion Mode NEGATIVE
Units AUC

Chromatography:

Chromatography ID:CH003871
Chromatography Summary:C18 iP REVERSE PHASE
Instrument Name:Waters Acquity
Column Name:Waters ACQUITY UPLC HSS T3 (150 x 2.1mm,1.8um)
Column Temperature:40
Flow Gradient:The gradient started with 5% of solvent B and 95% solvent A and remained at 5% B until 2 min post injection. A linear gradient to 37% B was carried out until 7 min and increased to 41% until 14 min. Between 14 and 26 minutes the gradient increased to 95% of B and remained at 95% B for 4 minutes. At 30 min the gradient returned to 5% B. The chromatography was stopped at 40 min
Flow Rate:0.25 ml/min
Solvent A:100% water; 10mM tributylamine; 15mM acetic acid
Solvent B:100% methanol
Chromatography Type:Reversed phase

MS:

MS ID:MS004852
Analysis ID:AN005115
Instrument Name:Thermo Q Exactive Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:El-Maven polly, ThermoFisher Xcalibur, Metabolites were annotated based on the in-house metabolite library- elution time and m/z values
Ion Mode:NEGATIVE
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