A Quantitative Assessment of The Yeast Lipidome using Electrospray Ionization Mass Spectrometry

Materials and methods

1. Yeast strains and growth conditions
   The wild-type strain BY4742 (MATα his3Δ1 leu2Δ0 lys2Δ0 ura3Δ0) was grown in rich YEPD medium (1% yeast extract, 2% peptone, 2% glucose). Cells were cultured at 30°C with rotational shaking at 200 rpm in Erlenmeyer flasks at a "flask volume/medium volume" ratio of 5:1.
2. Storage of yeast cells for lipid extraction
   
   1. A 50 ml culture of cells was harvested by centrifugation at 3000 x g for 5 minutes.
   2. Washed two times with cold water.
      1. Resuspend pellet in 25 ml ice cold water
      2. Pellet cells in centrifuge at 3000 x g for 5 minutes
   3. Resuspend the pellet and transfer to eppendorf tube
   4. Pellet by centrifugation, 16,000 x g for 2 minutes, remove supernatant and freeze  at -80°C until use. (we use a beaker of isopropyl alcohol kept in the -80 freezer, liquid nitrogen can also be used)
3. Reagents
   Biotech grade chloroform and methanol were from Sigma-Aldrich. Free fatty acids and triacylglycerols were purchased from Larodan (Malmo, Sweden). Various species of phospholipids - including phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, phosphatidylserine, phosphatidic acid, and cardiolipins - were obtained from Avanti Polar Lipid (Alabaster, AL, USA). High-speed glass centrifuge tubes with Teflon lined caps were from Fisher.

Lipid extraction

This is a modification of the protocol described by Bligh and Dyer⁸. All manipulations with extracted lipids should be done using glass pipettes or syringes; plastics will create a large background signal if they come into contact with chloroform. The exact volumes are not critical as long as the ratios of 1:2:0.8 for chloroform - MeOH - H₂O at step 3 and 2:2:1.8 for chloroform - MeOH - H₂O at step 7 are conserved.

1. Resuspend frozen cells in 1.6 ml of ice-cold distilled H₂O.
2. Transfer 1.6 ml of the cell suspension to high-speed glass centrifuge tubes.
3. Add 6 ml of chloroform and MeOH (1:2) mix and 0.8 ml of glass beads to the cell suspension.
4. Vortex the cell suspension with glass beads two times for 1 min.
5. Add 2 ml of chloroform and mix gently.
6. Incubate for 5 min at room temperature with occasional mixing.
7. Add 2 ml of distilled H₂O and mix gently.
8. Incubate for 5 min at room temperature with occasional mixing.
9. Centrifuge for 5 min at 3000 x g at room temperature.
10. Collect the entire liquid phase into a new high-speed glass centrifuge tube.
11. Add 3.2 ml of chloroform to the cell pellets from step 9.
12. Vortex two times for 1 min.
13. Centrifuge for 5 min at 3000 x g at room temperature.
14. Add the supernatant to the liquid phase from step 10.
15. Centrifuge for 5 min at 3000 x g at room temperature.
16. Discard the upper (aqueous) phase and transfer the lower (organic) phase into a new high-speed glass centrifuge tube.
17. Centrifuge for 5 min at 3000 x g at room temperature.
18. Transfer the entire supernatant into a glass vial and dry under nitrogen.
19. Dissolve the lipid film in 500 μl of chloroform and store at -20°C.

Analysis of lipids by mass spectrometry

A stock mix of lipid standards in chloroform should be prepared beforehand as per Table 1, as well as a stock solution of MeOH - chloroform (1:1) with 0.1% (v/v) ammonium hydroxide.

1. Prior to injection, combine 10 μl of a sample with 10 μl of the standard mix of lipids provided in Table 1. In 200μL of 1:1 chloroform : methanol with 0.1% NH₄OH.
   • The standard to sample ratio can be changed as needed.
2. Resolve lipids using a Micromass Q-TOF 2 mass spectrometer equipped with a nano-electrospray source operating at a flow rate of 1 μl/min.
   • Exact instrument parameters will vary from instrument to instrument. See Table 2 for the settings for a Micromass Q-ToF 2 (Waters, Milford, MA, USA) equipped with a nano-electrospray source. Although we have taken advantage of the high resolution of a Q-TOF type of mass spectrometer, it is not a mandatory requirement.
3. After acquisition the mass spectra are smoothed, background subtracted and centred, and then the peak list exported to Excel. The peaks of each lipid class are then normalized to their internal standard. Depending on the application, it may be necessary do perform further post-processing such as deisotoping and deconvolution.

Table 1. Internal lipid standards, their concentrations in the standard mix, and the MS mode for their analysis.

Table 2. Instrument settings for a Micromass Q-ToF 2 (Waters, Milford, MA, USA) equipped with a nano-electrospray source.

This method enables a rapid quantitative assessment of the yeast lipidome using readily available, inexpensive materials. The method allows the identification of most of the lipid species found in yeast cells with the exception of diacylglycerols, ergosterols and ergosteryl esters, although these lipids can be identified by replacing ammonium hydroxide with lithium hydroxide. The described method enables lipid identification and quantification at the concentrations as low as μg/ml, with the concentration linearity spreading over 2 to 3 orders of magnitude (depending on lipid species). Although appropriate standards for phosphatidylinositol are not commercially available, the different molecular forms of this phospholipid can be assessed using standards for other phospholipid species.