With the recent development of higher energy collision-induced dissociation (HCD) even the low mass cut off problem of product ion spectra acquired in the LTQ could be overcome [30]. The Nanomate® provides plenty of time to be spent on each sample with only a few Selleck AG 13736 microliters of it consumed. This opens up the avenue for data-dependent acquisition of product ion spectra on all possible precursor ions, resulting in full scan precursor spectra and product ion spectra of literally every detectable lipid species at a resolution of 100,000 or more. Additionally, exact assignment of fatty acyl side chains can be achieved on a regular basis with this system. Quantitation is done Inhibitors,research,lifescience,medical by one

internal standard per lipid class [31], which is sufficient to compensate for varying ionization efficiencies. Figure 1 Schematic outline of a high throughput Inhibitors,research,lifescience,medical shotgun lipidomics platform consisting of an LTQ-Orbitrap mass spectrometer coupled to a NanoMate. An interesting alternative to gas chromatography-mass

spectrometry (GC-MS) analysis of fatty acids is published by the Welti group [32]. The CID-TOF system uses a quadrupole-TOF analyzer coupled to negative ESI direct infusion. Thereby mass selection in Q1 is turned off, Q2 fragments all ions and the TOF analyzer records intact fatty acid carboxylates with accurate mass. This provides Inhibitors,research,lifescience,medical the fingerprint of fatty acids including modified fatty acids without any prior derivatization step being necessary. Mentionable, this method only works for lipids which generate negative ions in ESI, but nevertheless comparison with Inhibitors,research,lifescience,medical GC-flame ionization detector (GC-FID) data shows good correlation [32]. 3. LC-MS 3.1. Low Resolution Mass Spectrometry The invention of ESI enabled

coupling of HPLC with mass spectrometry in a highly efficient manner for the first time [33]. This instrumental combination opened up completely new analytical perspectives in lipid research by combining the separation power of HPLC with the selectivity Inhibitors,research,lifescience,medical of mass spectrometry. Complex lipid classes like glycerolipids, glycerophospholipids or even glycolipids were analytically amenable on a regular basis by chromatography coupled to mass spectrometry, now termed LC-MS. Compared to direct infusion systems HPLC adds retention time as another layer of selectivity. Ketanserin On one hand this results in increased specificity for lipid identification, but on the other hand it complicates quantitation, because every spectrum in an LC-MS run has to be regarded as a single event with unique matrix effects and solvent composition (Figure 2). Therefore quantitative aspects are generally more difficult to be standardized than for direct infusion methods. Figure 2 (a) Total ion chromatogram of a lipid droplet extract acquired on C-18 reversed phase HPLC coupled to an LTQ-FT in positive ESI mode (b) consisting of 487 individual full scan mass spectra at a resolution of 200,000.