Summary of Study ST002751
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 PR001509. The data can be accessed directly via it's Project DOI: 10.21228/M8N71K 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 | ST002751 |
| Study Title | Biomolecular condensates create phospholipid-enriched microenvironments (Part 5) |
| Study Type | Metabolomes of mouse liver |
| Study Summary | In this study we used LC-MS and MS/MS to characterize the metabolomes of the input mouse liver metabolites used in the first two studies of this submission. |
| Institute | Cornell University |
| Department | Department of Pharmacology |
| Laboratory | Dr. Samie Jaffrey |
| Last Name | Dumelie |
| First Name | Jason |
| Address | 1300 York Ave, LC-524, New York City, NY |
| srj2003@med.cornell.edu | |
| Phone | 6465690174 |
| Submit Date | 2023-06-14 |
| Raw Data Available | Yes |
| Raw Data File Type(s) | mzdata.xml |
| Analysis Type Detail | LC-MS |
| Release Date | 2023-07-10 |
| Release Version | 1 |
Select appropriate tab below to view additional metadata details:
Project:
| Project ID: | PR001509 |
| Project DOI: | doi: 10.21228/M8N71K |
| Project Title: | Biomolecular condensates create phospholipid-enriched microenvironments |
| Project Type: | Metabolomics of in vitro condensates |
| Project Summary: | Proteins and RNA are able to phase separate from the aqueous cellular environment to form sub-cellular compartments called condensates. This process results in a protein-RNA mixture that is chemically distinct from the surrounding aqueous phase. Here we use mass spectrometry to characterize the metabolomes of condensates. To test this, we prepared mixtures of phase-separated proteins and cellular metabolites and identified metabolites enriched in the condensate phase. These proteins included SARS-CoV-2 nucleocapsid, as well as low complexity domains of MED1 and HNRNPA1. |
| Institute: | Cornell University |
| Department: | Department of Pharmacology |
| Laboratory: | Dr. Samie Jaffrey |
| Last Name: | Dumelie |
| First Name: | Jason |
| Address: | 1300 York Ave, LC-524, New York City, NY |
| Email: | jdumes98@gmail.com |
| Phone: | 6465690174 |
| Funding Source: | This work was supported by the National Institutes of Health grants R35NS111631 and R01CA186702 (S.R.J.); R01AR076029, R21ES032347 and R21NS118633 (Q.C.); and NIH P01 HD067244 and support from the Starr Cancer Consortium I13-0037 (S.S.G.). |
| Publications: | Under revision |
| Contributors: | Jason G. Dumelie, Qiuying Chen, Dawson Miller, Nabeel Attarwala, Steven S. Gross and Samie R. Jaffrey1 |
Subject:
| Subject ID: | SU002858 |
| Subject Type: | Mammal |
| Subject Species: | Mus musculus |
| Taxonomy ID: | 10090 |
| Species Group: | Mammals |
Factors:
Subject type: Mammal; Subject species: Mus musculus (Factor headings shown in green)
| mb_sample_id | local_sample_id | Factor |
|---|---|---|
| SA289465 | ANP_experiment_set_3_replicate_7 | 2 μl |
| SA289466 | ANP_experiment_set_3_replicate_8 | 2 μl |
| SA289467 | ANP_experiment_set_3_replicate_6 | 2 μl |
| SA289468 | ANP_experiment_set_3_replicate_5 | 2 μl |
| SA289469 | ANP_experiment_set_3_replicate_2 | 2 μl |
| SA289470 | ANP_experiment_set_3_replicate_3 | 2 μl |
| SA289471 | ANP_experiment_set_3_replicate_4 | 2 μl |
| SA289472 | ANP_experiment_set_3_replicate_1 | 4 μl |
| Showing results 1 to 8 of 8 |
Collection:
| Collection ID: | CO002851 |
| Collection Summary: | Mouse metabolites were collected from the liver of female mice using methanol extraction. After euthanizing a mouse, the liver was immediately frozen in liquid nitrogen. We then used cold (-20C or colder) 80% methanol to extract metabolites. First, 1 ml of 80% methanol was added to the liver and incubated for 10 min at -20oC. Glass beads were added to the liver and then the liver was lysed by bead-beating for 45 s using a Tissuelyser cell disrupter (Qiagen). The lysate was incubated for 10 min at -20oC and centrifuged (13200 rpm, 5 min) to separate metabolites from macromolecules. The supernatant was collected and 200 µl of 80% methanol was added to the pellet. The incubation, shaking and centrifugation steps were repeated twice to extract more metabolites from the pellet. The three supernatants were combined and centrifuged (14000 rpm, 10 min) to separate any remaining macromolecules from the metabolites. The combined supernatants were dried using a SpeedVac Concentrator (Savant, SPD131DDA) at 25oC and the dried metabolite samples were stored at -80oC. |
| Sample Type: | Liver |
| Collection Method: | 80% methanol |
| Storage Conditions: | -80℃ |
Treatment:
| Treatment ID: | TR002867 |
| Treatment Summary: | All samples were treated identically for this sub-study, except a higher volume (4 μl ANP_experiment_set_3_replicate_1) of one sample was injected than for the other samples (2 μl). |
Sample Preparation:
| Sampleprep ID: | SP002864 |
| Sampleprep Summary: | On the day of metabolite analysis, dried-down extracts were reconstituted in 150 µl 70% acetonitrile, at a relative protein concentration of ~ 2 µg/µl. Either 4 µl (replicate 1) or 2 µl (all other replicates) of this reconstituted extract was injected for LC/MS-based targeted and untargeted metabolite profiling. |
| Extract Storage: | -80℃ |
Chromatography:
| Chromatography ID: | CH003350 |
| Chromatography Summary: | Tissue extracts were analyzed by LC/MS as described previously, using a platform comprised of an Agilent Model 1290 Infinity II liquid chromatography system coupled to an Agilent 6550 iFunnel time-of-flight MS analyzer. Chromatography of metabolites utilized aqueous normal phase (ANP) chromatography on a Diamond Hydride column (Microsolv). Mobile phases consisted of: (A) 50% isopropanol, containing 0.025% acetic acid, and (B) 90% acetonitrile containing 5 mM ammonium acetate. To eliminate the interference of metal ions on chromatographic peak integrity and electrospray ionization, EDTA was added to the mobile phase at a final concentration of 5 µM. The following gradient was applied: 0-1.0 min, 99% B; 1.0-15.0 min, to 20% B; 15.0 to 29.0, 0% B; 29.1 to 37min, 99% B. |
| Instrument Name: | Agilent Model 1290 Infinity II liquid chromatography system |
| Column Name: | Cogent Diamond Hydride (150 × 2.1 mm, 4um) |
| Column Temperature: | 26 |
| Flow Gradient: | The following gradient was applied: 0-1.0 min, 99% B; 1.0-15.0 min, to 20% B; 15.0 to 29.0, 0% B; 29.1 to 37min, 99% B. |
| Flow Rate: | 0.3 mL/min |
| Solvent A: | 50% isopropanol/50% water; 0.025% acetic acid |
| Solvent B: | 90% acetonitrile/10% water; 5 mM ammonium acetate |
| Chromatography Type: | Normal phase |
Analysis:
| Analysis ID: | AN004463 |
| Analysis Type: | MS |
| Chromatography ID: | CH003350 |
| Num Factors: | 2 |
| Num Metabolites: | 45 |
| Rt Units: | Minutes |
| Units: | Ion abundance (peak area) |
| Analysis ID: | AN004464 |
| Analysis Type: | MS |
| Chromatography ID: | CH003350 |
| Num Factors: | 2 |
| Num Metabolites: | 113 |
| Rt Units: | Minutes |
| Units: | Ion abundance (peak area) |
