Ceramide - ESI-MS/MS - Liebisch et al.

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Line 54: Line 54:
* MS/MS-conditions:
* MS/MS-conditions:
** precursor ion scan of m/z 264.2
** precursor ion scan of m/z 264.2
-
** multiple reaction monitoring table
+
** multiple reaction monitoring table of species observed frequently
{| border="1" class="wikitable" style="text-align:center"
{| border="1" class="wikitable" style="text-align:center"
! Analyte !! Precursor [m/z] !! Precursor [m/z] !! Collision energy [eV]  
! Analyte !! Precursor [m/z] !! Precursor [m/z] !! Collision energy [eV]  
 +
|-
 +
! Cer 14:0 - H2O
 +
| 492.5|| 264.2 ||x
|-
|-
! Cer 14:0  
! Cer 14:0  

Revision as of 16:21, 6 June 2008

Contents

Sample preparation

  • lipid extraction according to Bligh and Dyer
  • internal standards are added prior lipid extraction
  • to avoid the loss of lipids, extraction was performed in glassware
  • samples are dissolved in methanol containing 5 mM ammonium formate/chloroform (3/1 = v/v)
Material Material used Internal Standard(s) Internal Standard(s) added
Cultured cells 100µg protein Cer 14:0, Cer 17:0 50ng each
Human plasma 20µl Cer 14:0, Cer 17:0 50ng each

Instrumentation and method

Pump

  • Type: binary high pressure gradient (Agilent 1100)
  • Mode: isocratic flow gradient
  • Solvent(s): 5 mM ammonium formate/chloroform (3/1 = v/v)
  • Gradient:
Time [min] Flow [ml/min]  % Solvent A  % Solvent B
0 0.05 100 0
0.1 0.03 100 0
1.1 0.2 100 0
1.3 0.05 100 0

Autosampler

  • Type: CTC Pal
  • Injection volume: 20µl
  • Wash solvent: methanol/chloroform = 1/1

Mass spectrometer

  • Type: Triple quadrupole (Micromass, Quattro Ultima)
  • Ionization mode: ESI positive
  • Ionization voltage:
  • Source temperature:
  • Collision gas: Argon
  • Collision gas pressure:
  • MS/MS-conditions:
    • precursor ion scan of m/z 264.2
    • multiple reaction monitoring table of species observed frequently
Analyte Precursor [m/z] Precursor [m/z] Collision energy [eV]
Cer 14:0 - H2O 492.5 264.2 x
Cer 14:0 510.5 264.2 x

Data analysis and quantification

Data handling

Isotope correction

Calibration and quantification

Method validation

Accuracy

Precision

LOD

LOQ

Recovery

Sample data

Mass spectra

Chromatogram

Reference

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