Sphingolipid profiling - LC-MS/MS - Scherer et al.
From LipidomicsWiki
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== Instrumentation and method == | == Instrumentation and method == | ||
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=== Pump === | === Pump === | ||
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*Type: binary and isocratic pump (Agilent 1200) | *Type: binary and isocratic pump (Agilent 1200) | ||
*Mode: gradient elution | *Mode: gradient elution | ||
- | *Solvent(s): Solvent A water containing 0.2% formic acid and 200 mM ammonium formate ; Solvent B acetonitrile containing 0.2% formic acid | + | *Solvent(s): Solvent A water containing 0.2% formic acid and 200 mM ammonium formate ; Solvent B acetonitrile containing 0.2% formic acid |
*Gradient: | *Gradient: | ||
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*Type: Interchim HILIC column (Interchim, Montlucan, France) | *Type: Interchim HILIC column (Interchim, Montlucan, France) | ||
*length: 50 x 2 mm i.d., 0.5 µm pre-column filter | *length: 50 x 2 mm i.d., 0.5 µm pre-column filter | ||
- | *Particle size: 1.8 µm | + | *Particle size: 1.8 µm |
*Column temperature: 50°C | *Column temperature: 50°C | ||
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**multiple reaction monitoring table of species observed frequently | **multiple reaction monitoring table of species observed frequently | ||
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! Analyte | ! Analyte |
Revision as of 12:33, 27 April 2010
Contents |
Sample preparation
- S1P and LPA were extracted with butanol
- internal standards were added prior lipid extraction
- supernatant was transferred to a glass vial and injected
Material | Material used | Internal Standard(s) | Internal Standard(s) added |
---|---|---|---|
Cell homogenate | 100µg | SPH d17:1 | 20 ng |
SPC d17:1 | 2 ng | ||
GluCer 12:0 | 20 ng | ||
LacCer 12:0 | 20 ng | ||
Cer1P 12:0 | 20 ng |
Instrumentation and method
Pump
- Type: binary and isocratic pump (Agilent 1200)
- Mode: gradient elution
- Solvent(s): Solvent A water containing 0.2% formic acid and 200 mM ammonium formate ; Solvent B acetonitrile containing 0.2% formic acid
- Gradient:
Time [min] | Flow [ml/min] | % Solvent A | % Solvent B |
---|---|---|---|
0 | 0.8 | 0 | 100 |
0.1 | 0.8 | 0 | 100 |
0.11 | 0.8 | 10 | 90 |
2.5 | 0.8 | 50 | 50 |
3.5 | 0.8 | 50 | 50 |
3.51 | 0.8 | 0 | 100 |
4.5 | 0.8 | 0 | 100 |
Autosampler
- Type: CTC Pal
- Injection volume: 10µl
- Wash solvent 1: Isopropanol/MeOH (1/1; v/v), Wash solvent 2: MeOH
Column
- Type: Interchim HILIC column (Interchim, Montlucan, France)
- length: 50 x 2 mm i.d., 0.5 µm pre-column filter
- Particle size: 1.8 µm
- Column temperature: 50°C
Mass spectrometer
- Type: Triple quadrupole (Applied Biosystems, 4000 QTRAP)
- Ionization mode: ESI negative
- Ionization voltage: -4500V
- Source temperature: 300°C
- Collision gas: Nitrogen
- Collision gas pressure: medium
- MS/MS-conditions:
- precursor ion scan of m/z 153 for LPA species screening
- multiple reaction monitoring table of species observed frequently
Analyte | Precursor [m/z] | Product [m/z] | Collision energy [eV] |
---|---|---|---|
S1P | 378.2 | 79 | 58V |
SA1P | 380.2 | 79 | 58V |
13C2D2-S1P | 382.2 | 79 | 58V |
LPA 16:0 | 409.2 | 153 | 30V |
LPA 18:0 | 437.2 | 153 | 30V |
LPA 18:1 | 435.2 | 153 | 30V |
LPA 18:2 | 433.2 | 153 | 30V |
LPA 20:4 | 457.2 | 153 | 30V |
LPA 17:0 | 423.2 | 153 | 30V |
Data analysis and quantification
Software
- Analyst 1.4.2.
Calibration and quantification
- calibration type: matrix calibration - addition of naturally occurring species
- species used for calibration
Species | Human plasma |
---|---|
S1P | 0.352-3.518µmol/L |
SA1P | 0.175-1.75µmol/L |
LPA 16:0 | 0.162-1.62µmol/L |
LPA 18:0 | 0.0304-0.304µmol/L |
LPA 18:1 | 0.0917-0.917µmol/L |
LPA 18:2 | 0.308-3.08µmol/L |
LPA 20:4 | 0.291-2.91µmol/L |
Method Validation
Accuracy
90 - 106 %
Precision
CV: 3 % - 10 %
LOD
6 nmol/L for S1P, SA1P and <2nmol/l
Recovery
85% (S1P, SA1P); 80 % LPA
Sample data
Mass spectra
Chromatogram