Abstract:In this work mixed hybrid phospholipid bilayers (mhBLM) were deposited on fluorine doped tin oxide (FTO) films. Two component silane‐based self‐assembled monolayers (SAMs) formed on FTO surface trigger vesicle fusion and formation of mhBLMs which are stable, can be easily regenerated, and therefore, used for multiple experiments. We found that certain chemical and physical conditions under which mixed SAMs are fabricated translate into functional properties of mhBLMs. In all cases we observed interaction of me… Show more
“…4, properties of mhBLM does not change over 18 h. Previously, a similar experiment was carried out using methyltrichlorosilane (MTS) as a backfiller [14]. The authors showed (see supporting information [14]) that the membrane is stable over hours and pore forming toxins can be incorporated into the membrane. Therefore, mhBLMs obtained in this study can be applied for the incorporation of pore forming toxins as well.…”
Section: Resultsmentioning
confidence: 91%
“…During the hydrolysis reaction between silane and oxide surface strong Si-O-Sn bonds are formed which contribute to robust SAM formation [13]. One important advantage of silanised oxide surfaces is suitability for multi-cycle hybrid bilayer lipid membrane formation and regeneration [4,6,14,15], particularly due to the strength of the Si-O-Sn bond. In contrary, for the gold/ alkylthiol system, the phospholipid bilayer could not be immobilised several times because a mixed monolayer rearranges to packed islands of long alkylchain molecules up to 72 h exposure to an aqueous solution [2].…”
Section: Introductionmentioning
confidence: 99%
“…In the current study, following the methodology which was employed for the assembly of tethered bilayers on thin gold film supports [3], we raised the research question if sufficient fluidity of bilayers immobilised on the metal oxide surface can be achieved by designing the mixed hybrid phospholipid bilayer membrane (mhBLM) [14]. In particular, by designing the mixed self-assembled silane monolayers consisting of short chain spacers and long alkyl chain anchor molecules we expected that such anchor layer would allow the formation of tethered bilayer providing a sufficient flexibility of the proximal to a surface phospholipid monolayer for the functional reconstitution of transmembrane proteins.…”
In this work, we attempted to design phospholipid bilayers tethered to semiconducting metal oxide films. The phospholipid layers assembled on compact monocomponent self-assembled monolayers (SAM) on oxide films were accomplished earlier; however, previous studies indicated a poor ability of these layers to functionally reconstitute transmembrane proteins. Commercially available fluorine doped tin oxide (FTO) sheet glass was chosen as a model solid support. FTO surface was functionalised utilising by the mixture of the long and short chain hydrophobic silanes. Specifically, octadecyltrichlorosilane (OTS) and vinyltrimethoxysilane (VTS) were used to assemble mixed silane-based SAMs on FTO. Exposure of mixed SAMs to a solution of multilamellar vesicles of 1,2-dioleoylsn- glycero-3-phosphocholine (DOPC) and 40% cholesterol triggered the changes of electrochemical parameters commensurate with the formation of additional dielectric layers of phospholipids.
“…4, properties of mhBLM does not change over 18 h. Previously, a similar experiment was carried out using methyltrichlorosilane (MTS) as a backfiller [14]. The authors showed (see supporting information [14]) that the membrane is stable over hours and pore forming toxins can be incorporated into the membrane. Therefore, mhBLMs obtained in this study can be applied for the incorporation of pore forming toxins as well.…”
Section: Resultsmentioning
confidence: 91%
“…During the hydrolysis reaction between silane and oxide surface strong Si-O-Sn bonds are formed which contribute to robust SAM formation [13]. One important advantage of silanised oxide surfaces is suitability for multi-cycle hybrid bilayer lipid membrane formation and regeneration [4,6,14,15], particularly due to the strength of the Si-O-Sn bond. In contrary, for the gold/ alkylthiol system, the phospholipid bilayer could not be immobilised several times because a mixed monolayer rearranges to packed islands of long alkylchain molecules up to 72 h exposure to an aqueous solution [2].…”
Section: Introductionmentioning
confidence: 99%
“…In the current study, following the methodology which was employed for the assembly of tethered bilayers on thin gold film supports [3], we raised the research question if sufficient fluidity of bilayers immobilised on the metal oxide surface can be achieved by designing the mixed hybrid phospholipid bilayer membrane (mhBLM) [14]. In particular, by designing the mixed self-assembled silane monolayers consisting of short chain spacers and long alkyl chain anchor molecules we expected that such anchor layer would allow the formation of tethered bilayer providing a sufficient flexibility of the proximal to a surface phospholipid monolayer for the functional reconstitution of transmembrane proteins.…”
In this work, we attempted to design phospholipid bilayers tethered to semiconducting metal oxide films. The phospholipid layers assembled on compact monocomponent self-assembled monolayers (SAM) on oxide films were accomplished earlier; however, previous studies indicated a poor ability of these layers to functionally reconstitute transmembrane proteins. Commercially available fluorine doped tin oxide (FTO) sheet glass was chosen as a model solid support. FTO surface was functionalised utilising by the mixture of the long and short chain hydrophobic silanes. Specifically, octadecyltrichlorosilane (OTS) and vinyltrimethoxysilane (VTS) were used to assemble mixed silane-based SAMs on FTO. Exposure of mixed SAMs to a solution of multilamellar vesicles of 1,2-dioleoylsn- glycero-3-phosphocholine (DOPC) and 40% cholesterol triggered the changes of electrochemical parameters commensurate with the formation of additional dielectric layers of phospholipids.
“…16 Transmembrane proteins (vaginolysin, 56, 8 kDa) could not penetrate such rigid structure therefore, in further studies, long alkylchain OTS was diluted with methyltrichlorosilane (MTS), in order to produce less hydrophobic and less rigid SAM. 24 Relatively small peptide melittin (2, 6 kDa) did penetrate the membrane however, the lack of space between the solid support and the lipid bilayer, impeded reconstitution of α-hemolysin (33 kDa) to the membrane.…”
Section: Supplementary Materials For This Article Is Available Onlinementioning
Silane compound was synthesized via click chemistry and a mixture of synthesis products without purification was used to form the self-assembled monolayers on metal oxide conducting films of fluorine doped tin oxide (FTO). Silanized FTO surfaces triggered rupture of multilamellar vesicles and formed electrically insulating tethered bilayer membranes (tBLMs). In contrast to well-known hybrid bilayer membranes on silane monolayers such as ones formed from octadecyltrichlorosilane, tBLMs on FTO contained water-ion reservoir between solid surface and phospholipid bilayer sheet. They demonstrated biological relevance and ability to reconstitute the pore-forming protein channels such as α-hemolysin from Staphylococcus aureus and melittin. The addition of cholesterol to tBLMs decreased the membrane-damaging effect of melittin, while the opposite was observed in the case of α-hemolysin. The tBLMs can be regenerated multiple times without losing their functionality. The described methodology (both synthesis and formation of anchor monolayer) can be extended to any oxide film surface by properly adjusting chemical composition of molecular anchor and silanization conditions. This makes the proposed biomimetic membrane system attractive for various applications including biomedical sensors for the detection of pore-forming toxins.
“…In general most of the metal oxide semiconductors (MOS) such as RuO 2 [9,10], NiO [11], SnO 2 [12], MnO 2 [13,14], Fe 3 O 4 [15], CuO [16], ZnO [17], and CoO [18] are having a significant contribution for the SC applications [19]. Tin oxide (SnO 2 ) is well-known among MOS due to its vast applications such as in gas sensors [20,21], biosensors [22,23], solar cells [24,25], Li-ion battery materials [26,27], photocatalytic applications [28],…”
Tin oxide (SnO2) and nitrogen-doped graphene quantum dots (N-GQDs) composite nanotubes (SnO2/N-GQD NTs) were fabricated by the electrospinning technique and followed by the thermal annealing method for the application in supercapacitor as an electrode. SnO2/N-GQD NTs with different ratio of N-GQDs were prepared by adding different ratios of N-GQDs along with tin chloride during the electrospinning process. The prepared composite's structure and morphological properties were characterized by using different techniques like XRD, FE-SEM, TEM, and XPS. The supercapacitor performance of the SnO2/N-GQD NTs composite was analyzed by the electrochemical studies such as cyclic voltammetry and galvanostatic charge-discharge (GCD) measurement in 2 M KOH solution as electrolyte. The electrochemical analyses of SnO2/N-GQD NTs was tested at different scan rates and current densities. SnO2/N-GQD NTs prepared using 3 wt.% of N-GQDs showed an excellent capacity retention even after 5000 GCD cycles and exhibited a maximum specific capacitance of 420 mF g-1 at a current density of 8 mA cm-2 in comparison to pure SnO2 NTs (230 mF cm-2).
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