4.7 Article

QS21-Initiated Fusion of Liposomal Small Unilamellar Vesicles to Form ALFQ Results in Concentration of Most of the Monophosphoryl Lipid A, QS21, and Cholesterol in Giant Unilamellar Vesicles

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PHARMACEUTICS
卷 15, 期 9, 页码 -

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MDPI
DOI: 10.3390/pharmaceutics15092212

关键词

giant unilamellar vesicle; vaccine adjuvant; monophosphoryl lipid A; cholesterol; QS21; QS-21; membrane fusion; liposome

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ALFQ, a vaccine adjuvant preparation, is composed of liposomes containing saturated phospholipids, cholesterol, and two adjuvants MPLA and QS21. The addition of QS21 to nanoliposomes initiates a fusion reaction resulting in the formation of giant unilamellar vesicles (GUVs) with diameters >1.0 μm. The lipid composition analysis reveals that GUVs mainly contain cholesterol, MPLA, and QS21, suggesting that the binding of QS21 to cholesterol and the hydrophilicity of MPLA and QS21 may play important roles in the fusion process.
Army Liposome Formulation with QS21 (ALFQ), a vaccine adjuvant preparation, comprises liposomes containing saturated phospholipids, with 55 mol% cholesterol relative to the phospholipids, and two adjuvants, monophosphoryl lipid A (MPLA) and QS21 saponin. A unique feature of ALFQ is the formation of giant unilamellar vesicles (GUVs) having diameters >1.0 mu m, due to a remarkable fusion event initiated during the addition of QS21 to nanoliposomes containing MPLA and 55 mol% cholesterol relative to the total phospholipids. This results in a polydisperse size distribution of ALFQ particles, with diameters ranging from similar to 50 nm to similar to 30,000 nm. The purpose of this work was to gain insights into the unique fusion reaction of nanovesicles leading to GUVs induced by QS21. This fusion reaction was probed by comparing the lipid compositions and structures of vesicles purified from ALFQ, which were >1 mu m (i.e., GUVs) and the smaller vesicles with diameter <1 mu m. Here, we demonstrate that after differential centrifugation, cholesterol, MPLA, and QS21 in the liposomal phospholipid bilayers were present mainly in GUVs (in the pellet). Presumably, this occurred by rapid lateral diffusion during the transition from nanosize to microsize particles. While liposomal phospholipid recoveries by weight in the pellet and supernatant were 44% and 36%, respectively, higher percentages by weight of the cholesterol (similar to 88%), MPLA (94%), and QS21 (96%) were recovered in the pellet containing GUVs, and <= 10% of these individual liposomal constituents were recovered in the supernatant. Despite the polydispersity of ALFQ, most of the cholesterol, and almost all of the adjuvant molecules, were present in the GUVs. We hypothesize that the binding of QS21 to cholesterol caused new structural nanodomains, and subsequent interleaflet coupling in the lipid bilayer might have initiated the fusion process, leading to creation of GUVs. However, the polar regions of MPLA and QS21 together have a sugar lawn of ten sugars, the hydrophilicity of which might have provided a driving force for rapid lateral diffusion and concentration of the MPLA and QS21 in the GUVs.

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