TY - JOUR
T1 - Monitoring the morphological evolution of giant vesicles by azo dye-based sum-frequency generation (SFG) microscopy
AU - Momotake, Atsuya
AU - Mizuguchi, Takaha
AU - Hishida, Mafumi
AU - Yamamoto, Yasuhiko
AU - Yasui, Masato
AU - Nuriya, Mutsuo
N1 - Funding Information:
This work was supported by JSPS KAKENHI ( 16H01434 and 18K05312 ) and JST PRESTO ( JPMJPR17G6 ). We would like to thank Olympus Corporation for continuous support in the development of multiphoton microscopy. We would like to thank Enago ( www.enago.jp ) for the English language review. Appendix A
PY - 2020/2
Y1 - 2020/2
N2 - In the present work, dye-based sum-frequency generation (SFG) imaging using sodium 4-[4-(dibutylamino)phenylazo]benzenesulfonate (butyl orange, BO) as a new non-fluorescent specific azo dye is employed to monitor the morphological evolution of giant vesicles (GVs). After loading BO to the membrane of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) single-component GVs, the outermost membranes were clearly visualized using SFG microscopy, which provided images of the distinct outer and inner faces of the lipid bilayers. In addition, SFG-active vesicles were detected also inside the GVs, depending on the dye concentrations. The dye-based SFG imaging technique provided experimental evidence that these oligolamellar vesicles containing an SFG-active interior had been formed after BO loading. The formation process of the oligolamellar vesicles with inner SFG-active vesicles was successfully monitored, and their formation mechanism was discussed.
AB - In the present work, dye-based sum-frequency generation (SFG) imaging using sodium 4-[4-(dibutylamino)phenylazo]benzenesulfonate (butyl orange, BO) as a new non-fluorescent specific azo dye is employed to monitor the morphological evolution of giant vesicles (GVs). After loading BO to the membrane of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) single-component GVs, the outermost membranes were clearly visualized using SFG microscopy, which provided images of the distinct outer and inner faces of the lipid bilayers. In addition, SFG-active vesicles were detected also inside the GVs, depending on the dye concentrations. The dye-based SFG imaging technique provided experimental evidence that these oligolamellar vesicles containing an SFG-active interior had been formed after BO loading. The formation process of the oligolamellar vesicles with inner SFG-active vesicles was successfully monitored, and their formation mechanism was discussed.
KW - Azo dye
KW - Giant vesicle
KW - Lipid bilayer
KW - Non-Fluorescent dye
KW - SFG
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U2 - 10.1016/j.colsurfb.2019.110716
DO - 10.1016/j.colsurfb.2019.110716
M3 - Article
C2 - 31865122
AN - SCOPUS:85076551650
VL - 186
JO - Colloids and Surfaces B: Biointerfaces
JF - Colloids and Surfaces B: Biointerfaces
SN - 0927-7765
M1 - 110716
ER -