Ergosterol is mainly located in the cytoplasmic leaflet of the yeast plasma membrane

Lukasz M. Solanko, David P. Sullivan, Yves Y. Sere, Maria Szomek, Anita Lunding, Katarzyna A. Solanko, Azra Pizovic, Lyubomir D. Stanchev, Thomas Günther Pomorski*, Anant K. Menon, Daniel Wüstner

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

53 Scopus citations

Abstract

Transbilayer lipid asymmetry is a fundamental characteristic of the eukaryotic cell plasma membrane (PM). While PM phospholipid asymmetry is well documented, the transbilayer distribution of PM sterols such as mammalian cholesterol and yeast ergosterol is not reliably known. We now report that sterols are asymmetrically distributed across the yeast PM, with the majority (~80%) located in the cytoplasmic leaflet. By exploiting the sterol-auxotrophic hem1Δ yeast strain we obtained cells in which endogenous ergosterol was quantitatively replaced with dehydroergosterol (DHE), a closely related fluorescent sterol that functionally and accurately substitutes for ergosterol in vivo. Using fluorescence spectrophotometry and microscopy we found that <20% of DHE fluorescence was quenched when the DHE-containing cells were exposed to membrane-impermeant collisional quenchers (spin-labeled phosphatidylcholine and trinitrobenzene sulfonic acid). Efficient quenching was seen only after the cells were disrupted by glass-bead lysis or repeated freeze-thaw to allow quenchers access to the cell interior. The extent of quenching was unaffected by treatments that deplete cellular ATP levels, collapse the PM electrochemical gradient or affect the actin cytoskeleton. However, alterations in PM phospholipid asymmetry in cells lacking phospholipid flippases resulted in a more symmetric transbilayer distribution of sterol. Similarly, an increase in the quenchable pool of DHE was observed when PM sphingolipid levels were reduced by treating cells with myriocin. We deduce that sterols comprise up to ~45% of all inner leaflet lipids in the PM, a result that necessitates revision of current models of the architecture of the PM lipid bilayer.

Original languageEnglish (US)
Pages (from-to)198-214
Number of pages17
JournalTraffic
Volume19
Issue number3
DOIs
StatePublished - Mar 2018

Funding

We acknowledge support from the Villum Fonden (grant 022868)(T.G. P. and D.W.), and the Qatar National Research Fund (NPRP 7-082-1-014)(A.K.M.). We thank Fred Maxfield for the use of a fluorescence microscope to image DHE in the quenching experiments with 4-SLPC, the Abby and Howard P. Milstein Chemistry Core Facility at Weill Cornell Medical College for synthesis of 4-SLPC, Magdalena Marek for generating yeast deletion mutants, and Neha Chauhan and Michael Timme for comments on the manuscript. A.K.M. acknowledges Sam Canis for critical input and Sidse Babett Knudsen for stimulation.

Keywords

  • TNBS
  • asymmetry
  • collisional quenching
  • dehydroergosterol
  • ergosterol
  • fluorescence
  • heme
  • plasma membrane
  • yeast

ASJC Scopus subject areas

  • Genetics
  • Molecular Biology
  • Structural Biology
  • Biochemistry
  • Cell Biology

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