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Membrane Protein Production in Yeast: Modification of Yeast Membranes for Human Membrane Protein Production

  • Anita Emmerstorfer-Augustin
  • Tamara Wriessnegger
  • Melanie Hirz
  • Guenther Zellnig
  • Harald PichlerEmail author
Protocol
Part of the Methods in Molecular Biology book series (MIMB, volume 1923)

Abstract

Approximately 30% of the genes in the human genome code for membrane proteins, and yet we know relatively little about these complex molecules. Therefore, the biochemical and structural characterization of this challenging class of proteins represents an important frontier in both fundamental research and advances in drug discovery. However, due to their unique physical properties and requirement for association with cellular membranes, expression in heterologous systems is often daunting. In this chapter we describe how to engineer the yeast Pichia pastoris to obtain humanized sterol compositions. By implementing some simple genetic engineering approaches, P. pastoris can be reprogrammed to mainly produce cholesterol instead of ergosterol. We show how to apply mass spectrometry to confirm the production of cholesterol instead of ergosterol and how we have further analyzed the strain by electron microscopy. Finally, we delineate how to apply and test the cholesterol-forming P. pastoris strain for functional expression of mammalian Na,K-ATPase α3β1 isoform. Na,K-ATPases have been shown to specifically interact with cholesterol and phospholipids, and, obviously, the presence of cholesterol instead of ergosterol was the key to stabilizing correct localization and activity of this ion transporter.

Key words

Yeast Pichia pastoris Sterols Human membrane protein expression Membrane engineering 

Notes

Acknowledgments

This work has been supported by the Federal Ministry for Digital and Economic Affairs (bmwd); the Federal Ministry for Transport, Innovation, and Technology (bmvit); the Styrian Business Promotion Agency SFG, the Standortagentur Tirol, Government of Lower Austria, and ZIT Technology Agency of the City of Vienna through the COMET-funding program managed by the Austrian Research Promotion Agency FFG and by the Austrian Science Fund (FWF) project J3787 (A. E.-A.). The funding agencies had no influence on the conduct of this research.

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  • Anita Emmerstorfer-Augustin
    • 1
  • Tamara Wriessnegger
    • 2
  • Melanie Hirz
    • 3
  • Guenther Zellnig
    • 4
  • Harald Pichler
    • 2
    • 3
    Email author
  1. 1.Division of Biochemistry, Biophysics and Structural Biology, Department of Molecular and Cell BiologyUniversity of CaliforniaBerkeleyUSA
  2. 2.acib-Austrian Centre of Industrial BiotechnologyGrazAustria
  3. 3.Institute of Molecular Biotechnology, Graz University of Technology, NAWI Graz, BioTechMed GrazGrazAustria
  4. 4.Institute of Plant Sciences, University of Graz, NAWI GrazGrazAustria

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