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Thermo exactive orbitrap mass spectrometer

Manufactured by Thermo Fisher Scientific
Sourced in United Kingdom

The Thermo Exactive Orbitrap mass spectrometer is a high-resolution, accurate-mass instrument designed for a wide range of analytical applications. It utilizes Orbitrap mass analyzer technology to provide precise mass measurements and high-quality data. The core function of the Thermo Exactive Orbitrap is to perform mass spectrometry analysis for the identification and quantification of compounds in complex samples.

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4 protocols using thermo exactive orbitrap mass spectrometer

1

Ceramide Profiling of Organoid Samples

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Organoid samples were sonicated in phosphate buffered saline (pH7.4) and then extracted according to the method of Folch
et al.26 (link). The samples were analysed by liquid chromatography-mass spectrometry (LC-MS) on a Thermo Exactive Orbitrap mass spectrometer (Thermo Scientific, Hemel Hempsted, UK) coupled to a Thermo Accela 1250 ultra high pressure liquid chromatography (UHPLC) system. Samples were injected on to C18 column (Thermo Hypersil Gold, 2.1 mm x 100 mm, 1.9 μm) and separated using a water/acetonitrile/isopropanol gradient
27 (link). Ceramide 17:0 (Avanti Polar Lipids, Alabaster, AL, USA) was included as an internal standard. Ion signals corresponding to individual ceramide molecular species were extracted from raw LC-MS data sets. Concentration of ceramide was expressed as pmol/mg after normalisation to mg of wet weight tissue.
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2

Quantitative Lipidomics Analysis of Glucosylceramide

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Cellular lipids were extracted in methanol/chloroform (2:1, v/v). The lipids were analyzed by liquid chromatography-mass spectrometry (LC-MS) using a Thermo Exactive Orbitrap mass spectrometer (Thermo Scientific, Hemel Hempstead, UK), equipped with a heated electrospray ionization probe and coupled to a Thermo Accela 1250 UHPLC system. The samples were analyzed in positive and negative ion modes over m/z 200-2000. Injections (1 µl) were made onto a Thermo Hypersil Gold C18 column (1.9 μm; 2.1 mm × 100 mm). Mobile phase A consisted of water containing 10 mM ammonium formate and 0.1% (v/v) formic acid. Mobile phase B consisted of 90:10 isopropanol/acetonitrile containing 10 mM ammonium formate and 0.1% (v/v) formic acid. The initial conditions for the analysis were 65%A/35%B. The percentage of mobile phase B was increased to 100% over 10 min and held for 7 min before re-equilibration with the starting conditions for 4 min. The LC-MS data were processed with Progenesis QI software v2.0 (Non-Linear Dynamics, Newcastle upon Tyne, UK) and searched against LIPID MAPS (www.lipidmaps.org/) and the Human Metabolome Database (http://www.hmdb.ca/) for identification. The mean abundance of identified molecular species of glucosylceramide within the study groups was calculated from the normalised positive ion data sets.
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3

Lipid Profiling of 3T3-L1 Adipocytes

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Extraction of 3T3-L1 adipocyte lipids was performed according to the method described by Folch et al. [32] (link). The lipids were analysed by liquid chromatography–mass spectrometry (LC–MS) using a Thermo Orbitrap Exactive mass spectrometer (Thermo Scientific, Hemel Hempstead, UK), equipped with a heated electrospray ionization (HESI) probe and coupled to a Thermo Accela 1250 UHPLC system. All samples were analysed in both positive and negative ion mode over the mass to charge (m/z) range 200–2000. The samples were injected on to a Thermo Hypersil Gold C18 column (2.1 mm × 100 mm, 1.9 μm). Mobile phase A consisted of water containing 10 mM ammonium formate and 0.1% (v/v) formic acid. Mobile phase B consisted of 90:10 isopropanol/acetonitrile containing 10 mM ammonium formate and 0.1% (v/v) formic acid. The initial conditions for analysis were 65%A/35%B. The percentage of mobile phase B was increased to 100% over 10 minutes and held for 7 min before re-equilibration with the starting conditions for 4 min. All solvents were LC–MS grade (Fisher Scientific, Loughborough, UK). The raw LC–MS data were processed with Progenesis CoMet v2.0 software (Non-linear Dynamics, Newcastle, UK) and searched against LIPID MAPS (www.lipidmaps.org) for identification.
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4

High-Resolution Mass Spectrometry Protocols

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Mass spectra were acquired on a Thermo
Orbitrap Exactive mass spectrometer (Thermo Scientific, San Jose,
CA). In the conventional atmospheric ESI source configuration a standard
heated capillary interface was used as illustrated in Figure 1a. The temperature of the heated capillary inlet
was adjusted from 150 to 300 °C, and the dc voltages on the tube
lens and skimmer were adjusted to achieve either optimal sensitivity
or ionization gentleness. The instrument was tuned using the LTQ Velos ESI positive ion calibration
solution (Thermo Scientific, San Jose, CA). In the SPIN source configuration
the ESI emitter was moved to the first vacuum region of the mass spectrometer
and positioned at the entrance of the ion funnel.15 (link),18 (link) As depicted in Figure 1b, in this configuration
the standard ion optics up to lens L0 were replaced by two ion funnels
operating at different vacuum pressures. Independent of the source
configuration the instrument was always operated in ultrahigh-resolution
mode with an m/z range of 200–3000
with a 3 microscan average per spectrum. The AGC was set for high
dynamic range with a maximum ion injection time of 100 ms. Electrospray
emitters were fabricated by chemically etching fused-silica capillary
tubing with a 10 μm i.d. and 150 μm o.d. (Polymicro Technologies,
Phoenix, AZ) as described previously.24 (link)
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