Electrochemical Impedance Spectroscopy Based Evaluation of Chlorophyll a Reconstitution within Tethered Bilayer Lipid Membrane

被引:2
|
作者
Liustrovaite, Viktorija [1 ]
Valiuniene, Ausra [1 ]
Valincius, Gintaras [2 ]
Ramanavicius, Arunas [1 ,3 ]
机构
[1] Vilnius Univ, Fac Chem & Geosci, Dept Phys Chem, LT-03225 Vilnius, Lithuania
[2] Vilnius Univ, Life Sci Ctr, Inst Biochem, LT-10257 Vilnius, Lithuania
[3] Ctr Phys Sci & Technol, Lab Nanotechnol, State Res Inst, LT-10257 Vilnius, Lithuania
关键词
Electrochemical Engineering; Hybrid device; Organic Electrochemistry; Nanoscale materials; Nanoclusters; Membranes and Separators; Luminescence; FLUORESCENCE; FUSION;
D O I
10.1149/1945-7111/ac0262
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
This article reports electrochemical impedance spectroscopy-based evaluation of chlorophyll a (Chl-a) reconstitution within tethered bilayer lipid membrane (tBLM), formed on a gold surface by vesicle fusion. The self-assembled monolayer (SAM) consisting of a mixture of WC14 (20-tetradecyloxy-3,6,9,12,15,18,22-heptaoxahexatricontane-1-thiol) and beta-mercaptoethanol (beta ME) mixed in a molar % ratio of 35:65 served as a molecular anchor for tBLMs. The fluorescence microscopy (FM) allowed direct observation of incorporation of Chl-a into membranes. The lipid composition consisting of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and cholesterol (Chol), was found to be highly compatible with the addition of Chl-a to the phospholipid membranes at different molar ratios. Moreover, the addition of Chl-a to DOPC yielding DOPC (50%)/Chol (40%)/Chl-a (10%) bilayers consistently decreased defect density in tBLMs, thus increasing dielectric integrity of the membranes. Also, we observed a significant structural stabilization of tBLMs subject to bias potential variation in experiments involving Chl-a containing bilayers.
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页数:6
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