Design, construction, and characterization of high-performance membrane fusion devices with target-selectivity

© 2011 American Chemical Society

Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 28(2012), 4 vom: 31. Jan., Seite 2299-305
1. Verfasser: Kashiwada, Ayumi (VerfasserIn)
Weitere Verfasser: Yamane, Iori, Tsuboi, Mana, Ando, Shun, Matsuda, Kiyomi
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2012
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Boronic Acids Liposomes Peptides benzeneboronic acid L12H7B02G5
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245 1 0 |a Design, construction, and characterization of high-performance membrane fusion devices with target-selectivity 
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520 |a Membrane fusion proteins such as the hemagglutinin glycoprotein have target recognition and fusion accelerative domains, where some synergistically working elements are essential for target-selective and highly effective native membrane fusion systems. In this work, novel membrane fusion devices bearing such domains were designed and constructed. We selected a phenylboronic acid derivative as a recognition domain for a sugar-like target and a transmembrane-peptide (Leu-Ala sequence) domain interacting with the target membrane, forming a stable hydrophobic α-helix and accelerating the fusion process. Artificial membrane fusion behavior between the synthetic devices in which pilot and target liposomes were incorporated was characterized by lipid-mixing and inner-leaflet lipid-mixing assays. Consequently, the devices bearing both the recognition and transmembrane domains brought about a remarkable increase in the initial rate for the membrane fusion compared with the devices containing the recognition domain alone. In addition, a weakly acidic pH-responsive device was also constructed by replacing three Leu residues in the transmembrane-peptide domain by Glu residues. The presence of Glu residues made the acidic pH-dependent hydrophobic α-helix formation possible as expected. The target-selective liposome-liposome fusion was accelerated in a weakly acidic pH range when the Glu-substituted device was incorporated in pilot liposomes. The use of this pH-responsive device seems to be a potential strategy for novel applications in a liposome-based delivery system 
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700 1 |a Yamane, Iori  |e verfasserin  |4 aut 
700 1 |a Tsuboi, Mana  |e verfasserin  |4 aut 
700 1 |a Ando, Shun  |e verfasserin  |4 aut 
700 1 |a Matsuda, Kiyomi  |e verfasserin  |4 aut 
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