Summary of Study ST001894

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 PR001192. The data can be accessed directly via it's Project DOI: 10.21228/M8MX3X This work is supported by NIH grant, U2C- DK119886.

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Study IDST001894
Study TitleInvolvement of Mieap in cardiolipin metabolism (part II)
Study SummaryMass spectrometric data of Cardiolipin in Mice kidney (Mieap-WT vs. Mieap-KO), and Mice liver (Mieap-WT vs. Mieap-KO)
Institute
National Cancer Center Japan Research Institute
Last NameIkari
First NameNaoki
Address5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan
Emailnikari@ncc.go.jp
Phone+81-3-3542-2511
Submit Date2021-07-30
Analysis Type DetailLC-MS
Release Date2021-08-09
Release Version1
Naoki Ikari Naoki Ikari
https://dx.doi.org/10.21228/M8MX3X
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN003075
Analysis type MS
Chromatography type Reversed phase
Chromatography system UltiMate 3000 (Thermo Fisher Scientific)
Column Waters XBridge C18 (150 x 1.0mm,3.5um)
MS Type ESI
MS instrument type Orbitrap
MS instrument name Thermo Q Exactive Orbitrap
Ion Mode NEGATIVE
Units pmol/mg

MS:

MS ID:MS002862
Analysis ID:AN003075
Instrument Name:Thermo Q Exactive Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:Analyses were performed on a LC/MS/MS system consisting of a Q-Exactive Plus mass spectrometer (Thermo Fisher Scientific) equipped with an electrospray ionization source, and an UltiMate 3000 system (Thermo Fisher Scientific). The lipid samples were separated on Waters X-Bridge C18 column (3.5 μm, 150 mm × 1.0 mm i.d.) at 40°C using a gradient solvent system as follows: mobile phase A (isopropanol/methanol/water (5:1:4, v/v/v) supplemented with 5 mM ammonium formate and 0.05% ammonium hydroxide (28% in water))/mobile phase B (isopropanol supplemented with 5 mM ammonium formate and 0.05% ammonium hydroxide (28% in water)) ratios of 60%/40% (0 min), 40%/60% (1 min), 20%/80% (9 min), 5%/95% (11-30 min), 95%/5% (31-35 min) and 60%/40% (45 min). Flow rate was 25 μL/min. The source and ion transfer parameters applied were as followed: spray voltage 3.0 kV. For negative ionization modes, the sheath gas and the capillary temperature were maintained at 60 and 320 °C, respectively. The Orbitrap mass analyzer was operated at a resolving power of 70,000 in full-scan mode (scan range: 200–1800 m/z; automatic gain control (AGC) target:3e6) and of 35,000 in the Top 20 data-dependent MS2 mode (stepped normalized collision energy: 20, 30 and 40; isolation window: 4.0 m/z; AGC target: 1e5). Identification of CL molecular species was performed using with LipidSearch4.2 software (Mitsui knowledge industry).
Ion Mode:NEGATIVE
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