SE126:/S2/M1

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Sample Set Information

ID SE126
Title Test dataset for MS-DIAL 2.0 and MS-FINDER 2.0
Description Three validation kits are prepared for the evaluation of MS-DIAL 2.0 and MS-FINDER 2.0.

(1) The validation of MS-DIAL chromatogram deconvolution for GC/MS data was performed by six raw data files from five major MS vendors.
(2) Software comparison of MS-DIAL against other alternative programs was performed by four raw data files.
(3) Software comparison of MS-FINDER against other alternative programs was performed by five EI-MS spectra.

The raw files except for Bruker Daltonics and Thermo Fisher Scientific (because of their contracts) can be downloaded.

Authors Zijuan Lai, Hiroshi Tsugawa, Gert Wohlgemuth, Matthew Mueller, Yuxuan Zheng, Atsushi Ogiwara, Sajjan Mehta, John Meissen, Kohei Takeuchi, Tobias Kind, Peter Beal, Masanori Arita, Oliver Fiehn
Reference Lai et al. (2018) Nature Methods Jan;15(1):53-56. doi: 10.1038/nmeth.4512
Comment


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The raw data files are available at DROP Met web site in PRIMe database of RIKEN.

Sample Information

ID S2
Title human plasma
Organism - Scientific Name Homo sapiens
Organism - ID NCBI taxonomy 9606
Compound - ID
Compound - Source
Preparation
Sample Preparation Details ID
Comment

Analytical Method Information

ID M1
Title Agilent GC-Q(MS)
Method Details ID MS2
Sample Amount 1 μl
Comment The biological sample was NIST standard human plasma; analysis procedures were done according to the “Agilent GC-Quadrupole MS” protocol from a previous report.

Fiehn, O. Curr. Protoc. Mol. Biol. 114, 30.4.1–30.4.32 (2016)


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Analytical Method Details Information

ID MS2
Title Agilent GC-Q(MS)
Instrument Agilent GC-quadrupole MS
Instrument Type
Ionization EI
Ion Mode Positive
Description Extraction procedures

All metabolite extraction procedures were kept on ice, and the quantities for sample aliquots were 25 μL for blood plasma, 5 x 10^6 for cells, 5 mg for tissues, and 2 mL for algae cultures. Metabolites were extracted with 1,000 μL of degassed acetonitrile:isopropanol:water (3:3:2, v/v/v) and then homogenized, centrifuged, decanted, and evaporated. Extracts were cleaned with 500 μL of degassed acetonitrile:water (1:1, v/v) to remove triglycerides and membrane lipids, and evaporated again. For GC-MS analysis, internal standard C8–C30 fatty acid methyl esters were added to determine the retention index. The dried samples were derivatized with 10 μL of methoxyamine hydrochloride (or ethoxyamine hydrochloride) in pyridine and subsequently by 90 μL of MSTFA (or MSTFA-d9) for trimethylsilylation of acidic protons.

The biological sample was NIST standard human plasma; analysis procedures were done according to the “Agilent GC-Quadrupole MS” protocol from a previous report.

Comment_of_details Fiehn, O. Curr. Protoc. Mol. Biol. 114, 30.4.1–30.4.32 (2016)


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