Targeting of proteins involved in sterol biosynthesis to lipid particles of the yeast Saccharomyces cerevisiae
Autor: | Dagmar Zweytick, Günther Daum, Regina Leber, Heidemarie Müllner, Friederike Turnowsky |
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Rok vydání: | 2004 |
Předmět: |
Saccharomyces cerevisiae Proteins
Squalene monooxygenase Saccharomyces cerevisiae Biophysics Protein targeting medicine.disease_cause Biochemistry medicine Intramolecular Transferases Sterol biology Endoplasmic reticulum Lipid particle Lipid metabolism Methyltransferases Cell Biology Lipid Metabolism biology.organism_classification Membrane contact site Recombinant Proteins Yeast Protein Structure Tertiary Cell biology Sterols Squalene Monooxygenase Oxygenases biology.protein lipids (amino acids peptides and proteins) Hydrophobic and Hydrophilic Interactions Subcellular Fractions Lanosterol synthase |
Zdroj: | Biochimica et Biophysica Acta (BBA) - Biomembranes. 1663(1-2):9-13 |
ISSN: | 0005-2736 |
DOI: | 10.1016/j.bbamem.2004.03.001 |
Popis: | In the yeast Saccharomyces cerevisiae, three enzymes of the sterol biosynthetic pathway, namely Erg1p, Erg6p and Erg7p, are located in lipid particles. Whereas Erg1p (squalene epoxidase) is also present in the endoplasmic reticulum (ER) to a significant amount, only traces of Erg6p (sterol C-24 methyltransferase) and Erg7p (lanosterol synthase) are found in the ER. We have chosen these three Erg-proteins as typical representatives of lipid particle proteins to study targeting to their destination. Lipid particle proteins do not contain obvious targeting motifs, but the only common structural feature is the presence of one or two hydrophobic domains near the C-termini. We constructed truncated versions of Erg1p, Erg6p and Erg7p to test the role of these hydrophobic domains in subcellular distribution. Our results demonstrate that lack of the hydrophobic domains prevents at least in part the association of the proteins with lipid particles and causes their retention to the ER. This result strongly supports the view that ER and lipid particles are related organelles. |
Databáze: | OpenAIRE |
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