“…[15][16][17] Also the rate and nature of electron transfer process may be realized by manipulating the organizations of their complex molecular assemblies at a nanometer scale. DNA has already been used to prepare some supramolecular network as the building block for assembling of redox protein namely, Cytochrome c (Cyt c) into multilayers 18 via layer-layer-layer self-assembly method. However, there was no such efficient and precise control of molecular orientation as well as the spatial distribution of redox-active centres of protein in the complex architectures.…”
Section: Introductionmentioning
confidence: 99%
“…However, there was no such efficient and precise control of molecular orientation as well as the spatial distribution of redox-active centres of protein in the complex architectures. Although this ordered DNA network has some potential for their role in direct electron transport through redox proteins 18 but their industrial applications may be limited due to comparably less control over the molecular engineering of DNA assemblies onto solid substrate. Therefore, more experimental sophistication may be necessary which may require additional cost for large-scale of such nanofabrication.…”
We present the formation of a complex molecular network consisting of highly water soluble λ-DNA and a redox protein, Cytochrome c (Cyt c), at the air–water interface by Langmuir–Blodgett technique.
“…[15][16][17] Also the rate and nature of electron transfer process may be realized by manipulating the organizations of their complex molecular assemblies at a nanometer scale. DNA has already been used to prepare some supramolecular network as the building block for assembling of redox protein namely, Cytochrome c (Cyt c) into multilayers 18 via layer-layer-layer self-assembly method. However, there was no such efficient and precise control of molecular orientation as well as the spatial distribution of redox-active centres of protein in the complex architectures.…”
Section: Introductionmentioning
confidence: 99%
“…However, there was no such efficient and precise control of molecular orientation as well as the spatial distribution of redox-active centres of protein in the complex architectures. Although this ordered DNA network has some potential for their role in direct electron transport through redox proteins 18 but their industrial applications may be limited due to comparably less control over the molecular engineering of DNA assemblies onto solid substrate. Therefore, more experimental sophistication may be necessary which may require additional cost for large-scale of such nanofabrication.…”
We present the formation of a complex molecular network consisting of highly water soluble λ-DNA and a redox protein, Cytochrome c (Cyt c), at the air–water interface by Langmuir–Blodgett technique.
“…17 Agarose gel electrophoresis of ct DNA revealed that it was a mixture of fragments of varying size (Fig. S1 †).…”
Section: Resultsmentioning
confidence: 98%
“…Cyclic voltammetry of multilayer assemblies showed quasi-reversible ET, a substantial amount of electro-active protein (up to 320 pmol cm −2 for a 6 bi-layer system) and only minor changes in the formal redox potential (E f ) of cyt c, indicating that the heme remains in the native state. 17 Compared to other multilayer systems (built using synthetic polyelectrolytes or modified nanoparticles [37][38][39] ) the cyt c-DNA system showed the highest accumulation of redox active material. Exploiting these properties, cyt c-DNA multilayer systems were advanced to construct analytical signal chains.…”
Artificial assemblies consisting of the cationic cytochrome c (cyt c) and double-stranded DNA are interesting for the field of biohybrid systems because of the high electro-activity of the incorporated redox protein. However, little is known about the interactions between these two biomolecules. Here, the complex of reduced cyt c and a 41 base pair oligonucleotide was characterized in solution as a function of pH and ionic strength. Persistent cyt c-DNA agglomerates were observed by UV-vis and DLS (dynamic light scattering) at pH 5.0 and low ionic strength. The strength of the interaction was attenuated by raising the pH or the ionic strength. At pH 7.0 agglomerates were not formed, allowing interaction analysis by NMR spectroscopy. Using TROSY (transverse relaxation-optimized spectroscopy)-HSQC (heteronuclear single quantum coherence) experiments it was possible to identify the DNA binding site on the cyt c surface. Numerous residues surrounding the exposed heme edge of cyt c were involved in transient binding to DNA under these conditions. This result was supported by SEC (size exclusion chromatography) experiments at pH 7.0 showing that the interaction is sufficient for co-elution of cyt c and DNA.
“…A large number of works were carried to immobilize this protein on an electrode surface successfully [12][13][14][15][16], but there is still a need to increase the functional density beyond the monolayer arrangement. To achieve this aim, Cyt c immobilized on vertically aligned carbon nanofibers [17] and Cyt c multilayers within a polyelectrolyte [18,19], DNA [20], and protein [21] assembly by layer-by-layer arrangement have been developed. However, in thicker films or multilayers, generally only those protein molecules near the electrode surface are electro-active.…”
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