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Stefanie Vehring

Researcher at Humboldt University of Berlin

Publications -  6
Citations -  316

Stefanie Vehring is an academic researcher from Humboldt University of Berlin. The author has contributed to research in topics: Endoplasmic reticulum & Flippase. The author has an hindex of 5, co-authored 6 publications receiving 304 citations.

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StarD10, a START domain protein overexpressed in breast cancer, functions as a phospholipid transfer protein.

TL;DR: Evidence is provided that StarD10 interacts with phosphatidylcholine (PC) andosphatidylethanolamine (PE) by electron spin resonance measurement and preferentially selects lipid species containing a palmitoyl or stearoyl chain on the sn-1 and an unsaturated fatty acyl chain (18:1 or 18:2) on thesn-2 position.
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Flippase activity detected with unlabeled lipids by shape changes of giant unilamellar vesicles.

TL;DR: It is demonstrated that shape change of giant unilamellar vesicles (GUVs) can be used as a new tool to study the occurrence and time scale of flippase-mediated transbilayer movement of unlabeled phospholipids.
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New fluorescent probes reveal that flippase-mediated flip-flop of phosphatidylinositol across the endoplasmic reticulum membrane does not depend on the stereochemistry of the lipid.

TL;DR: Results show that the flippase is able to translocate all four PI isomers and that both glycerol isomers of PI flip-flop across the ER membrane at rates similar to that measured for fluorescence-labeled phosphatidylcholine.

phosphatidylinositol across the endoplasmic reticulum membrane does not depend on the stereochemistry of the lipid

TL;DR: In this paper, the authors investigate whether the endoplasmic reticulum (ER) flippase recognizes the glycerophospholipids that it transports, and they show that the flippases is able to translocate all four diastereoisomers of PI across the ER membrane at rates similar to that measured for fluorescence-labeled phosphatidylcholine.
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Flip-Flop of Fluorescently Labeled Phospholipids in Proteoliposomes Reconstituted with Saccharomyces cerevisiae Microsomal Proteins

TL;DR: It is found that the protein translocon is not required for transbilayer movement of phospholipids across the ER, and yeast is defined as a promising model system for future attempts to identify the ER phosphorus flippase and to test and purify candidate flippases.