Summary of Study ST000221

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 PR000181. The data can be accessed directly via it's Project DOI: 10.21228/M8R30R This work is supported by NIH grant, U2C- DK119886.

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Study IDST000221
Study TitleNormal plasma cells,Low proliferation multiple myeloma and High proliferation multiple myeloma cells
Study Typedifferential metabolomics
Study SummaryCD138 sorted bone marrow plasma cell were obtained from a normal patient, a multiple myelow with slow proliferation and a multiple myelow with rapid proliferation.
Institute
Mayo Clinic
DepartmentHematology
Last NameGonsalves
First NameWilliam
EmailDasari.Surendra@mayo.edu
Submit Date2015-06-20
Num Groups1
Total Subjects1
Raw Data AvailableYes
Raw Data File Type(s)d
Uploaded File Size73 G
Analysis Type DetailLC-MS
Release Date2016-06-18
Release Version1
William Gonsalves William Gonsalves
https://dx.doi.org/10.21228/M8R30R
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR000181
Project DOI:doi: 10.21228/M8R30R
Project Title:Identification of altered metabolites in normal plasma cells, slow progression multiple myeloma and fast progression multiple meyloma
Project Type:Untargeted LC-MS Metabolomics
Project Summary:This experiment is comparing the metabolite profiles between normal plasma cells and clonal plasma cells from multiple myeloma patients.
Institute:Mayo Clinic
Department:Neurology
Last Name:Gonsalves
First Name:Wilson
Address:200 First Street SW, Rochester, MN 55905
Email:Dasari.Surendra@mayo.edu
Phone:507-284-0513

Subject:

Subject ID:SU000240
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Species Group:Mammals

Factors:

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

mb_sample_id local_sample_id Cognitive Status
SA010737BM049394SC004fast MM
SA010738BM049429SC001normal
SA010739BM049411SC003slow MM
Showing results 1 to 3 of 3

Collection:

Collection ID:CO000228
Collection Summary:Bone marrow cells were collected after fasting. Collected cells were CD138 sorted and frozen in -80C until analysis.
Sample Type:Bone marrow cells
Collection Location:Illiac crest

Treatment:

Treatment ID:TR000248

Sample Preparation:

Sampleprep ID:SP000242
Sampleprep Summary:1) Incubated cell pellets on ice for 15 min
2) Added PBS to cells and vortex well
3) Sonicate for 1 min in ice bath
4) Added MeOH+ACN mixture to cells and vortex well
5) Sonicated for 1 min in ice bath
6) Incubated on ice for 30 min + spin for 20 min at 18K RPM
7) Combined 110 ul from each sample into a pool sample (330 ul total)
8) Split pool into two fractions of 150 ul each (hilic & C18)
9) Split remaning sample into 150 ul x 2 (hilic & C18)

Chromatography:

Chromatography ID:CH000246
Chromatography Summary:C18
Chromatography Comments:Metabolite separation was achieved using an Acquity UPLC system (Waters, Milford, MA) with both hydrophilic interaction chromatography (HILIC) (ethylene-bridged hybrid 2.1150 mm, 1.7 mm; Waters) and reversed-phase liquid chromatography C18 (RPLC) (high-strength silica 2.1150 mm, 1.8 m; Waters). For each column, the run time was 20 min at a flow rate of 400 L/min. Reverse-phase chromatography was performed using 99% solvent A (5 mmol/L NH4 acetate, 0.1% formic acid, and 1% acetonitrile) to 100% solvent B (95% acetonitrile with 0.1% formic acid). The gradient was 0 min, 0% B; 1 min, 0% B; 3 min, 5% B; 13.0 min, 100% B; 16 min, 100% B; 16.5 min, 0% B; and 20 min, 0% B. The hydrophilic interaction chromatography gradient was as follows: 0 min, 100% B; 1 min, 100% B; 5 min, 90% B; 13.0 min, 0% B; 16 min, 0% B; 16.5 min, 100% B; and 20 min, 100% B. The injection volume of each sample was 5 L and column was maintained at 50C.
Instrument Name:Waters Acquity
Column Name:Waters high-strength silica (150 x 2.1mm,1.8um)
Chromatography Type:Reversed phase
  
Chromatography ID:CH000247
Chromatography Summary:HILIC
Chromatography Comments:Metabolite separation was achieved using an Acquity UPLC system (Waters, Milford, MA) with both hydrophilic interaction chromatography (HILIC) (ethylene-bridged hybrid 2.1150 mm, 1.7 mm; Waters) and reversed-phase liquid chromatography C18 (RPLC) (high-strength silica 2.1150 mm, 1.8 m; Waters). For each column, the run time was 20 min at a flow rate of 400 L/min. Reverse-phase chromatography was performed using 99% solvent A (5 mmol/L NH4 acetate, 0.1% formic acid, and 1% acetonitrile) to 100% solvent B (95% acetonitrile with 0.1% formic acid). The gradient was 0 min, 0% B; 1 min, 0% B; 3 min, 5% B; 13.0 min, 100% B; 16 min, 100% B; 16.5 min, 0% B; and 20 min, 0% B. The hydrophilic interaction chromatography gradient was as follows: 0 min, 100% B; 1 min, 100% B; 5 min, 90% B; 13.0 min, 0% B; 16 min, 0% B; 16.5 min, 100% B; and 20 min, 100% B. The injection volume of each sample was 5 L and column was maintained at 50C.
Instrument Name:Waters Acquity
Column Name:Waters ethylene-bridged hybrid (150 x 2.1mm,1.7um)
Chromatography Type:HILIC

Analysis:

Analysis ID:AN000327
Analysis Type:MS
Analysis Comments:Positive C18
Instrument Name:Agilent 6220 TOF MS
Chromatography ID:CH000246
Num Factors:3
Num Metabolites:33
Rt Units:Minutes
Units:Peak area
  
Analysis ID:AN000328
Analysis Type:MS
Analysis Comments:Negative C18
Instrument Name:Agilent 6220 TOF MS
Chromatography ID:CH000246
Num Factors:3
Num Metabolites:15
Rt Units:Minutes
Units:Peak area
  
Analysis ID:AN000329
Analysis Type:MS
Analysis Comments:Positive HILEC
Instrument Name:Agilent 6220 TOF MS
Chromatography ID:CH000247
Num Factors:3
Num Metabolites:104
Rt Units:Minutes
Units:Peak area
  
Analysis ID:AN000330
Analysis Type:MS
Analysis Comments:Negative HILEC
Instrument Name:Agilent 6220 TOF MS
Chromatography ID:CH000247
Num Factors:3
Num Metabolites:53
Rt Units:Minutes
Units:Peak area
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