Visualizing Loss of Plasma Membrane Lipid Asymmetry Using Annexin V Staining

被引:2
|
作者
Baum, Julia F. [1 ,2 ]
Uzun, Huriye D. [1 ,2 ]
Pomorski, Thomas Gunther [1 ,2 ]
机构
[1] Ruhr Univ Bochum, Fac Chem & Biochem, Dept Mol Biochem, Bochum, Germany
[2] Univ Copenhagen, Dept Plant & Environm Sci, Frederiksberg, Denmark
来源
BIO-PROTOCOL | 2023年 / 13卷 / 14期
关键词
Confocal microscopy; Giant vesicle; Lipid asymmetry; Lipid-binding protein; Mammalian cells; Plasma membrane; UNILAMELLAR VESICLES GUVS; FLOW-CYTOMETRIC DETECTION; PHOSPHATIDYLSERINE EXPRESSION; SELECTIVE AFFINITY; APOPTOTIC CELLS; EXPOSURE; PROTEINS; PHOSPHOLIPIDS; FLIPPASES; PEPTIDES;
D O I
10.21769/BioProtoc.4754
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Loss of plasma membrane lipid asymmetry contributes to many cellular functions and responses, including apoptosis, blood coagulation, and cell fusion. In this protocol, we describe the use of fluorescently labeled annexin V to detect loss of lipid asymmetry in the plasma membrane of adherent living cells by fluorescence microscopy. The approach provides a simple, sensitive, and reproducible method to detect changes in lipid asymmetry but is limited by low sample throughput. The protocol can also be adapted to other fluorescently labeled lipid-binding proteins or peptide probes. To validate the lipid binding properties of such probes, we additionally describe here the preparation and use of giant unilamellar vesicles as simple model membrane systems that have a size comparable to cells.
引用
收藏
页数:15
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