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MB Sample ID: SA169562
Local Sample ID: | id_323 |
Subject ID: | SU001904 |
Subject Type: | Human |
Subject Species: | Homo sapiens |
Taxonomy ID: | 9606 |
Species Group: | Mammals |
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Combined analysis:
Analysis ID | AN002963 |
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Analysis type | MS |
Chromatography type | HILIC |
Chromatography system | Thermo Scientific Q-Exactive |
Column | SeQuant ZIC-HILIC (150 x 4.6mm,3.5um) |
MS Type | ESI |
MS instrument type | Orbitrap |
MS instrument name | Thermo Q Exactive Orbitrap |
Ion Mode | UNSPECIFIED |
Units | pmoles/l |
MS:
MS ID: | MS002753 |
Analysis ID: | AN002963 |
Instrument Name: | Thermo Q Exactive Orbitrap |
Instrument Type: | Orbitrap |
MS Type: | ESI |
MS Comments: | Untargeted metabolomics analysis was conducted on 100µl of serum at Metabolon, Inc (Durham, NC, USA) with ultrahigh performance liquid chromatography-tandem mass spectroscopy (UPLC-MS/MS). The method utilized an ultra-performance liquid chromatography (UPLC) and a Thermo Scientific Q-Exactive high resolution/accurate mass spectrometer interfaced with a heated electrospray ionization (HESI-II) source and Orbitrap mass analyzer operated at 35,000 mass resolution. One aliquot was analyzed using acidic positive ion conditions, chromatographically optimized for more hydrophilic compounds; the extract compound was gradient eluted from a C18 column using water and methanol, containing 0.05% perfluoropentanoic acid (PFPA) and 0.1% formic acid (FA). Another aliquot was analyzed with the prior approach but it was chromatographically optimized for more hydrophobic compounds and operated at an overall higher organic content. A third aliquot was analyzed using basic negative ion optimized conditions using a separate dedicated C18 column. The basic extracts were gradient eluted from the column using methanol and water, however with 6.5mM Ammonium Bicarbonate at pH 8. The fourth aliquot was analyzed via negative ionization following elution from a HILIC column using a gradient consisting of water and acetonitrile with 10mM Ammonium Formate, pH 10.8. The MS analysis alternated between MS and data-dependent MSn scans using dynamic exclusion. The scan range between methods covered 70-1000 m/z. Raw data was extracted, peak-identified and QC processed using Metabolon’s hardware and software. Peaks were quantified using area-under-the-curve. Batch adjustment to correct variation resulting from instrument inter-day tuning differences was performed for each compound in run-day blocks by dividing by the median of the values for the experimental samples for each instrument run day, then multiplying these values by the original median. In one serum sample with a lower volume (65µl instead of 80µl), metabolite intensities were scaled accounting for the volume of serum available, under the assumption that metabolite signal intensities scale linearly with the sample volume. |
Ion Mode: | UNSPECIFIED |