Controlled Peptide-Mediated Vesicle Fusion Assessed by Simultaneous Dual-Colour Time-Lapsed Fluorescence Microscopy

• Published in: Scientific reports Vol. 10; no. 1; p. 3087
• Main Authors: Mora, Nestor Lopez, Boyle, Aimee L., Kolck, Bart Jan van, Rossen, Anouk, Pokorná, Šárka, Koukalová, Alena, Šachl, Radek, Hof, Martin, Kros, Alexander
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 20-02-2020; Nature Publishing Group
• Subjects: 14/19; 14/33; 631/57/2270; 631/92/314; Cholesterol; Cholesterol - chemistry; Color; Confocal microscopy; Dimerization; Drug delivery; Fluorescence; Fluorescence microscopy; Fluorescence Resonance Energy Transfer; Humanities and Social Sciences; Lipid bilayers; Lipids; Lipids - chemistry; Lipopeptides - chemistry; Membrane Fusion; Microscopy; Microscopy, Confocal; Microscopy, Fluorescence - methods; multidisciplinary; Peptides; Peptides - chemistry; Polysorbates - chemistry; Science; Science (multidisciplinary); SNAP receptors; Spectrometry, Fluorescence; Unilamellar Liposomes - chemistry; Vesicle fusion
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-59926-z

We have employed a model system, inspired by SNARE proteins, to facilitate membrane fusion between Giant Unilamellar Vesicles (GUVs) and Large Unilamellar Vesicles (LUVs) under physiological conditions. In this system, two synthetic lipopeptide constructs comprising the coiled-coil heterodimer-forming peptides K
4
, (KIAALKE)
4
, or E
4
, (EIAALEK)
4
, a PEG spacer of variable length, and a cholesterol moiety to anchor the peptides into the liposome membrane replace the natural SNARE proteins. GUVs are functionalized with one of the lipopeptide constructs and the fusion process is triggered by adding LUVs bearing the complementary lipopeptide. Dual-colour time lapse fluorescence microscopy was used to visualize lipid- and content-mixing. Using conventional confocal microscopy, lipid mixing was observed on the lipid bilayer of individual GUVs. In addition to lipid-mixing, content-mixing assays showed a low efficiency due to clustering of K
4
-functionalized LUVs on the GUVs target membranes. We showed that, through the use of the non-ionic surfactant Tween 20, content-mixing between GUVs and LUVs could be improved, meaning this system has the potential to be employed for drug delivery in biological systems.