Summary of Study ST003271
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 PR002030. The data can be accessed directly via it's Project DOI: 10.21228/M86V58 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.
| Study ID | ST003271 |
| Study Title | Impact of serine supplementation following treatment with serine/glycine-depleted diet: Paw skin |
| Study Summary | We analyzed metabolites in the retina, choroid/RPE, plasma, and paw skin from mice that were previously on control or serine/glycine-depleted diet and then switched over to a control or serine-supplemented diet. This study contains paw skin samples. |
| Institute | Salk Institute for Biological Studies |
| Department | Molecular and Cell Biology Laboratory |
| Laboratory | Metallo Lab |
| Last Name | Lim |
| First Name | Esther |
| Address | 10010 N Torrey Pines Rd |
| ewlim2024@gmail.com | |
| Phone | (858) 453-4100 |
| Submit Date | 2024-06-15 |
| Num Groups | 4 |
| Total Subjects | 20 |
| Num Males | 20 |
| Raw Data Available | Yes |
| Raw Data File Type(s) | d |
| Analysis Type Detail | LC-MS |
| Release Date | 2024-07-10 |
| Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
| Project ID: | PR002030 |
| Project DOI: | doi: 10.21228/M86V58 |
| Project Title: | Metabolomic changes in mouse tissues following modulation of serine through the diet |
| Project Summary: | We analyzed metabolites in the retina, choroid/RPE, and plasma from WT and PHGDH heterozygous mice that were fed either a control or serine/glycine-deprived diet. Additionally, we also analyzed metabolites from the retina, choroid/RPE, paw skin, and plasma from mice that were previously on either a control or serine/glycine-deprived diet and then switched back to a control or serine-supplemented diet. |
| Institute: | Salk Institute |
| Department: | Molecular and Cell Biology Laboratory |
| Laboratory: | Metallo Lab |
| Last Name: | Lim |
| First Name: | Esther |
| Address: | 10010 N Torrey Pines Rd, La Jolla, CA, 92037, USA |
| Email: | ewlim2024@gmail.com |
| Phone: | (858) 453-4100 |
| Funding Source: | R01CA234245 |
Subject:
| Subject ID: | SU003391 |
| Subject Type: | Mammal |
| Subject Species: | Mus musculus |
| Taxonomy ID: | 10090 |
| Genotype Strain: | C57BL/6J |
| Age Or Age Range: | 12-16 months |
| Weight Or Weight Range: | 25-45 g |
| Gender: | Male |
| Animal Animal Supplier: | The Scripps Research Institute Vivarium |
| Animal Housing: | 5/cage |
| Animal Light Cycle: | 12h dark/12 h light |
| Animal Feed: | Special diets; see group labeling |
| Animal Water: | Ad libitum |
Factors:
Subject type: Mammal; Subject species: Mus musculus (Factor headings shown in green)
| mb_sample_id | local_sample_id | Treatment | Sample source |
|---|---|---|---|
| SA354419 | LMRI_DietRev_Skin_20J5 | Paw skin Control rescue | Mouse paw skin |
| SA354420 | LMRI_DietRev_Skin_20J4 | Paw skin Control rescue | Mouse paw skin |
| SA354421 | LMRI_DietRev_Skin_20J3 | Paw skin Control rescue | Mouse paw skin |
| SA354422 | LMRI_DietRev_Skin_20J2 | Paw skin Control rescue | Mouse paw skin |
| SA354423 | LMRI_DietRev_Skin_20J1 | Paw skin Control rescue | Mouse paw skin |
| SA354429 | LMRI_DietRev_Skin_20B3 | Paw skin control | Mouse paw skin |
| SA354430 | LMRI_DietRev_Skin_20C3 | Paw skin control | Mouse paw skin |
| SA354431 | LMRI_DietRev_Skin_20C2 | Paw skin control | Mouse paw skin |
| SA354432 | LMRI_DietRev_Skin_20B4 | Paw skin control | Mouse paw skin |
| SA354433 | LMRI_DietRev_Skin_20B2 | Paw skin control | Mouse paw skin |
| SA354424 | LMRI_DietRev_Skin_20H5 | Paw skin High serine rescue | Mouse paw skin |
| SA354425 | LMRI_DietRev_Skin_20H1 | Paw skin High serine rescue | Mouse paw skin |
| SA354426 | LMRI_DietRev_Skin_20H4 | Paw skin High serine rescue | Mouse paw skin |
| SA354427 | LMRI_DietRev_Skin_20H3 | Paw skin High serine rescue | Mouse paw skin |
| SA354428 | LMRI_DietRev_Skin_20H2 | Paw skin High serine rescue | Mouse paw skin |
| SA354414 | LMRI_DietRev_Skin_20D1 | Paw skin -SG diet | Mouse paw skin |
| SA354415 | LMRI_DietRev_Skin_20D2 | Paw skin -SG diet | Mouse paw skin |
| SA354416 | LMRI_DietRev_Skin_20D3 | Paw skin -SG diet | Mouse paw skin |
| SA354417 | LMRI_DietRev_Skin_20D4 | Paw skin -SG diet | Mouse paw skin |
| SA354418 | LMRI_DietRev_Skin_20D5 | Paw skin -SG diet | Mouse paw skin |
| Showing results 1 to 20 of 20 |
Collection:
| Collection ID: | CO003384 |
| Collection Summary: | Tissues were collected using Wollenberger clamps pre-cooled to the temperature of liquid nitrogen and stored at -80°C until analysis |
| Sample Type: | Skin |
Treatment:
| Treatment ID: | TR003400 |
| Treatment Summary: | Mice were fed control or serine/glycine-depleted (-SG) diet for 12 months. After 12 months, a subset of the mice that were on the -SG diet were switched back to either the control or supplemented diet for 4 months. |
Sample Preparation:
| Sampleprep ID: | SP003398 |
| Sampleprep Summary: | For sphingolipid extraction from retina and choroid/RPE, frozen tissue was homogenized with a ball mill (Retsch Mixer Mill MM 400) at 30 Hz for 3 min in 500 μl of −20°C methanol, 400 μl of ice-cold saline, and 100 μl of ice-cold MilliQ water, spiked with deuterated internal standards as described earlier. The mixture was then transferred into a 2-ml Eppendorf tube containing 1 ml of chloroform. The tubes were vortexed for 5 min and centrifuged at 16,000g at 4°C for 5 min. The lower organic phase was collected, and 2 μl of formic acid was added to the remaining polar phase, which was re-extracted with 1 ml of chloroform. Combined organic phases were dried and resuspended in 50 μl of 0.2% formic acid and 1 mM ammonium formate in methanol. Last, the tubes were sonicated in a bath sonicator for 10 min and spun at 16,000g for 10 min at 4°C. For plasma, 50 μl of plasma was extracted with 500 μl of −20°C methanol, 400 μl of saline, and 100 μl of water spiked with deuterated internal standards. Chloroform (1 ml) was then added to the tubes. The tubes were vortexed for 5 min and centrifuged at 16,000g at 4°C for 5 min. The lower organic phase was collected, and 2 μl of formic acid was added to the remaining polar phase, which was reextracted with 1 ml of chloroform. Combined organic phases were dried and resuspended in 100 μl of 0.2% formic acid and 1 mM ammonium formate in methanol. Next, the tubes were sonicated in a bath sonicator for 10 min and spun at 16,000g for 10 min at 4°C |
| Processing Storage Conditions: | Room temperature |
| Extract Storage: | 4℃ |
Combined analysis:
| Analysis ID | AN005357 |
|---|---|
| Analysis type | MS |
| Chromatography type | Reversed phase |
| Chromatography system | Agilent 6460 |
| Column | Peeke Scientific Spectra C8SR (150 x 3.0 mm, 3μm) |
| MS Type | ESI |
| MS instrument type | Triple quadrupole |
| MS instrument name | Agilent 6460 QQQ |
| Ion Mode | POSITIVE |
| Units | Normalized ion count/mg of protein |
Chromatography:
| Chromatography ID: | CH004058 |
| Chromatography Summary: | The gradient elution program consisted of the following profile: 0 min, 82% B; 3 min, 82% B; 4 min, 90% B, 18 min, 99% B; 25 min, 99%, 27 min, 82% B, 30 min, 82% B. |
| Instrument Name: | Agilent 6460 |
| Column Name: | Peeke Scientific Spectra C8SR (150 x 3.0 mm, 3μm) |
| Column Temperature: | 40°C |
| Flow Gradient: | 0 min, 82% B; 3 min, 82% B; 4 min, 90% B; 18 min, 99% B; 25 min, 99% B; 27 min, 82% B; and 30 min, 82% B |
| Flow Rate: | 0.5 mL/min |
| Solvent A: | 100% water; 0.2% formic acid; 2 mM ammonium formate |
| Solvent B: | 100% methanol; 0.2% formic acid; 1 mM ammonium formate |
| Chromatography Type: | Reversed phase |
MS:
| MS ID: | MS005087 |
| Analysis ID: | AN005357 |
| Instrument Name: | Agilent 6460 QQQ |
| Instrument Type: | Triple quadrupole |
| MS Type: | ESI |
| MS Comments: | Software: Agilent MassHunter Sphingolipid species were analyzed by selective reaction monitoring of the transition from precursor to product ions at associated optimized collision energies, and fragmentor voltages are provided elsewhere (https://doi.org/10.1007/978-1-60761-322-0_22). The m/z values of the precursor and product ions are provided in the metabolite metadata section. |
| Ion Mode: | POSITIVE |
