Electroformation of Giant Unilamellar Vesicles from Damp Lipid Films Formed by Vesicle Fusion

被引:5
作者
Boban, Zvonimir [1 ,2 ]
Mardesic, Ivan [1 ,2 ]
Jozic, Sanja Perinovic [3 ]
Sumanovac, Josipa [4 ]
Subczynski, Witold Karol [5 ]
Raguz, Marija [1 ]
机构
[1] Univ Split, Sch Med, Dept Med Phys & Biophys, Split 21000, Croatia
[2] Univ Split, Fac Sci, Doctoral Study Biophys, Split 21000, Croatia
[3] Univ Split, Fac Chem & Technol, Dept Organ Technol, Split 21000, Croatia
[4] Univ Split, Fac Sci, Dept Phys, Split 21000, Croatia
[5] Med Coll Wisconsin, Dept Biophys, Milwaukee, WI 53226 USA
关键词
GUV; electroformation; cholesterol; damp lipid film; rapid solvent exchange; plasma cleaning; cholesterol crystals; vesicle fusion; DOMAINS PRECEDES FORMATION; CHOLESTEROL CRYSTALS; PHASE-DIAGRAM; MEMBRANES; MIXTURES; PHOSPHATIDYLCHOLINE; EPR;
D O I
10.3390/membranes13030352
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Giant unilamellar vesicles (GUVs) are artificial membrane models which are of special interest to researchers because of their similarity in size to eukaryotic cells. The most commonly used method for GUVs production is electroformation. However, the traditional electroformation protocol involves a step in which the organic solvent is completely evaporated, leaving behind a dry lipid film. This leads to artifactual demixing of cholesterol (Chol) in the form of anhydrous crystals. These crystals do not participate in the formation of the lipid bilayer, resulting in a decrease of Chol concentration in the bilayer compared to the initial lipid solution. We propose a novel electroformation protocol which addresses this issue by combining the rapid solvent exchange, plasma cleaning and spin-coating techniques to produce GUVs from damp lipid films in a fast and reproducible manner. We have tested the protocol efficiency using 1/1 phosphatidylcholine/Chol and 1/1/1 phosphatidylcholine/sphingomyelin/Chol lipid mixtures and managed to produce a GUV population of an average diameter around 40 mu m, with many GUVs being larger than 100 mu m. Additionally, compared to protocols that include the dry film step, the sizes and quality of vesicles determined from fluorescence microscopy images were similar or better, confirming the benefits of our protocol in that regard as well.
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页数:12
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