A Fluorescence-based Assay for Measuring Phospholipid Scramblase Activity in Giant Unilamellar Vesicles
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A Fluorescence-based Assay for Measuring Phospholipid Scramblase Activity in Giant Unilamellar Vesicles. / Mathiassen, Patricia P. M.; Pomorski, Thomas Gunther.
I: Bio-protocol, Bind 12, Nr. 6, 4366, 2022.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - A Fluorescence-based Assay for Measuring Phospholipid Scramblase Activity in Giant Unilamellar Vesicles
AU - Mathiassen, Patricia P. M.
AU - Pomorski, Thomas Gunther
PY - 2022
Y1 - 2022
N2 - Transbilayer movement of phospholipids in biological membranes is mediated by a diverse set of lipid transporters. Among them are scramblases that facilitate rapid bi-directional movement of lipids without metabolic energy input. In this protocol, we describe the incorporation of phospholipid scramblases into giant unilamellar vesicles (GUVs) formed from scramblase-containing large unilamellar vesicles by electroformation. We also describe how to analyze their activity using membrane-impermeant sodium dithionite, to bleach symmetrically incorporated fluorescent ATT0488-conjugated phospholipids. The fluorescence-based readout allows single vesicle tracking for a large number of settled/immobilized GUVs, and provides a well-defined experimental setup to directly characterize these lipid transporters at the molecular level.
AB - Transbilayer movement of phospholipids in biological membranes is mediated by a diverse set of lipid transporters. Among them are scramblases that facilitate rapid bi-directional movement of lipids without metabolic energy input. In this protocol, we describe the incorporation of phospholipid scramblases into giant unilamellar vesicles (GUVs) formed from scramblase-containing large unilamellar vesicles by electroformation. We also describe how to analyze their activity using membrane-impermeant sodium dithionite, to bleach symmetrically incorporated fluorescent ATT0488-conjugated phospholipids. The fluorescence-based readout allows single vesicle tracking for a large number of settled/immobilized GUVs, and provides a well-defined experimental setup to directly characterize these lipid transporters at the molecular level.
KW - ATTO488
KW - Electroformation
KW - Dithionite
KW - Fluorescence microscopy
KW - Giant unilamellar vesicle
KW - Phospholipid scramblase
KW - Fluorescence bleaching
KW - ENDOPLASMIC-RETICULUM MEMBRANE
KW - FLIP-FLOP
KW - PHOSPHATIDYLSERINE
KW - ELECTROFORMATION
KW - RECONSTITUTION
KW - MECHANISMS
KW - PROTEINS
KW - EXPOSURE
U2 - 10.21769/BioProtoc.4366
DO - 10.21769/BioProtoc.4366
M3 - Journal article
C2 - 35434199
VL - 12
JO - Bio-protocol
JF - Bio-protocol
SN - 2331-8325
IS - 6
M1 - 4366
ER -
ID: 304158700