Control of Lipid Bilayer Phases of Cell-Sized Liposomes by Surface-Engineered Plasmonic Nanoparticles

Liquid-ordered (Lo)-phase domains, a cholesterol-rich area on lipid bilayers, have attracted significant attention recently because of their relevance to lipid rafts, the formation/collapse of which is associated with various kinds of information exchange through the plasma membrane. Here, we demons...

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Veröffentlicht in:Langmuir 2020-07, Vol.36 (26), p.7741-7746
Hauptverfasser: Nobeyama, Tomohiro, Shigyou, Kazuki, Nakatsuji, Hirotaka, Sugiyama, Hiroshi, Komura, Naoko, Ando, Hiromune, Hamada, Tsutomu, Murakami, Tatsuya
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container_end_page 7746
container_issue 26
container_start_page 7741
container_title Langmuir
container_volume 36
creator Nobeyama, Tomohiro
Shigyou, Kazuki
Nakatsuji, Hirotaka
Sugiyama, Hiroshi
Komura, Naoko
Ando, Hiromune
Hamada, Tsutomu
Murakami, Tatsuya
description Liquid-ordered (Lo)-phase domains, a cholesterol-rich area on lipid bilayers, have attracted significant attention recently because of their relevance to lipid rafts, the formation/collapse of which is associated with various kinds of information exchange through the plasma membrane. Here, we demonstrate that the formation/collapse of Lo-phase domains in cell-sized liposomes, that is, giant unilamellar vesicles (GUVs), can be controlled with bioactive plasmonic nanoparticles and light. The nanoparticles were prepared by surface modification of gold nanorods (AuNRs) using a cationized mutant of high-density lipoprotein (HDL), which is a natural cholesterol transporter. Upon the addition of surface-engineered AuNRs to GUVs with the mixed domains of Lo and liquid-disorder (Ld) phases, the Lo domains collapsed and solid-ordered (So)-phase domains were formed. The reverse phase transition was achieved photothermally, with the AuNRs loaded with cholesterol. During these transitions, the AuNRs appeared to be selectively localized on the less fluidic domain (Lo or So) in the phase-mixed GUVs. These results indicate that the phase transitions occur through the membrane binding of the AuNRs followed by spontaneous/photothermal transfer of cholesterol between the AuNRs and GUVs. Our strategy to develop bioactive AuNRs potentially enables spatiotemporal control of the formation/collapse of lipid rafts in living cells.
doi_str_mv 10.1021/acs.langmuir.0c00049
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title Control of Lipid Bilayer Phases of Cell-Sized Liposomes by Surface-Engineered Plasmonic Nanoparticles
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