The HPLC autosampler offers a higher degree of automatization than a syringe pump. Furthermore, it results in a short and concentrated sample pulse for about one minute, which can

be used for data acquisition with precursor ion and constant neutral loss scans. Depending on the number of scans necessary, multiple injections per sample are possible. Quantitation is achieved by a standard addition method with multiple standard curves, featuring one internal standard and sets of lipids with different fatty acyl chain lengths and degrees of unsaturation [18]. The method is very robust, highly automated and was applied on various subclasses of glycerophospholipids, Inhibitors,research,lifescience,medical sphingolipids and sterols [18,19,20,21]. As for all low resolution direct infusion technologies it runs into its limits when isobaric nominal mass compounds derived from the same phospholipid subclass occur, like, e.g., diacyl and acyl-alkyl glycerophospholipids. Another direct infusion approach encompasses coupling of a syringe pump and a triple Inhibitors,research,lifescience,medical quadrupole analyzer in multiple reaction monitoring (MRM) mode [22]. In this experimental setup, the anticipated precursor and product ions must Inhibitors,research,lifescience,medical be known. It allows a quick and reliable quantitation of major lipid components in a given lipid extract. On the downside, this method has a limited capability for detection of unexpected lipid species and is particularly vulnerable

for overlapping isobaric compounds. In contrast to low resolution instruments, high resolution mass Selleck Bcl2 inhibitor spectrometers deliver accurate mass and elemental composition of ions with very high confidence. Most lipid classes have an unambiguous fingerprint Inhibitors,research,lifescience,medical due to a certain and invariable number of the heteroatoms N, O, P and S. Due to this fact, the elemental composition Inhibitors,research,lifescience,medical of precursor and often also product ions contains highly valuable information about the lipid class. The Multiple Precursor Ion Scans (MPIS) method developed on a quadrupole-TOF instrument by the group of Shevchenko [23,24] combines high resolution precursor ion scans on glycerophospholipid headgroups and fatty acyl moieties, resulting in the individual fatty

acyl composition of glycerophospholipid species. The high resolving power is particularly helpful in the case of ambiguous product ions with mass differences in the first or second digit. The MPIS concept was successfully applied for quantitative global lipidome analysis in various cell systems almost including glycerophospholipids, glycerolipids, sphingolipids, sterols and various glycolipids [25,26,27]. The method has its limitations when one lipid class like triacylglycerol (TG) is present in bulk amounts and possibly suppresses ionization of other minor lipid classes [28]. A further development of the MPIS concept is shotgun lipidomics with a hybrid LTQ-Orbitrap instrument coupled to the Nanomate® ion source [29]. A schematic workflow of this platform is shown in Figure 1.

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