cytochrome-c-t and titanium-dioxide

Dissimilatory metal-reducing bacteria (DMRB) have a variety of c-type cytochromes (OM c-cyts) intercalated in their outer membrane, and this structure serves as the physiological basis for DMRB to carry out the extracellular electron transfer processes. Using Geobacter sulfurreducens as a model DMRB, we demonstrated that visible-light illumination could alter the electronic state of OM c-cyts from the ground state to the excited state in vivo. The existence of excited-state OM c-cyts in vivo was confirmed by spectroscopy. More importantly, excited-state OM c-cyts had a more negative potential compared to their ground-state counterparts, conferring DMRB with an extra pathway to transfer electrons to semi-conductive electron acceptors. To demonstrate this, using a TiO

Topics: Cell Membrane; Cytochromes c; Electron Transport; Extracellular Space; Geobacter; Light; Titanium

In this work, an efficient photoelectrochemical (PEC) biosensing platform has been designed and developed based on graphene (G) through modifying it into an electroconductive polymer nanosponge (EPNS) and with the incorporation of titanium dioxide nanowires (TiO2 NW) (designated as TiO2 (G) NW@EPNS). Functioning as an efficient immobilization matrix for immobilization of the enzyme Cytochrome C (Cyt C), TiO2 (G) NW@EPNS delivers features for an efficient PEC biosensor, such as fast kinetics of direct electron transfer (DET) to the electrode and effective separation of photogenerated holes and electrons. TiO

Topics: Biosensing Techniques; Cytochromes c; Electric Conductivity; Electrochemical Techniques; Enzymes, Immobilized; Equipment Design; Graphite; Models, Molecular; Nanowires; Nitrites; Photochemical Processes; Polymers; Titanium

A novel electrochemiluminescence (ECL) aptasensor was proposed for ultrasensitive detection of cytochrome c (cyt c) using CdS:Mn quantum dot-modified TiO2 nanowires (NWs) as electrode. The Mn-doped CdS was deposited on the TiO2 NWs by successive ion layer adsorption and reaction (SILAR) as ECL emitter, on which thiol-modified aptamer of cyt c was attached via Cd-S bond. Due to the high photo-electrical transfer efficiency, the as-prepared aptasensor shows high selectivity and sensitivity towards cyt c with a detection limit of 9.5fM and a linear range from 50fM to 125pM.

Topics: Aptamers, Nucleotide; Biosensing Techniques; Cadmium Compounds; Cytochromes c; Electrochemical Techniques; Luminescent Measurements; Manganese; Nanowires; Quantum Dots; Selenium Compounds; Titanium

In this work, a new electrochemical biosensor based on catalyzed hairpin assembly target recycling and cascade electrocatalysis (cytochrome c (Cyt c) and alcohol oxidase (AOx)) for signal amplification was constructed for highly sensitive detection of microRNA (miRNA). It is worth pointing out that target recycling was achieved only based on strand displacement process without the help of nuclease. Moreover, porous TiO2 nanosphere was synthesized, which could offer more surface area for Pt nanoparticles (PtNPs) enwrapping and enhance the amount of immobilized DNA strand 1 (S1) and Cyt c accordingly. With the mimicking sandwich-type reaction, the cascade catalysis amplification strategy was carried out by AOx catalyzing ethanol to acetaldehyde with the concomitant formation of high concentration of H2O2, which was further electrocatalyzed by PtNPs and Cyt c. This newly designed biosensor provided a sensitive detection of miRNA-155 from 0.8 fM to 1 nM with a relatively low detection limit of 0.35 fM.

Topics: Acetaldehyde; Alcohol Oxidoreductases; Aptamers, Nucleotide; Base Sequence; Biocompatible Materials; Biosensing Techniques; Catalysis; Citric Acid; Cytochromes c; Electrochemistry; Humans; Hydrogen Peroxide; MicroRNAs; Molecular Sequence Data; Nanoparticles; Oxidation-Reduction; Porosity; Reproducibility of Results; Signal Processing, Computer-Assisted; Titanium

Reactive oxygen species (ROS) generated by aerobic organisms are essential for physiological processes such as cell signaling, apoptosis, immune defense and oxidative stress mechanisms. Unbalanced oxidant/antioxidant budgets are involved in many diseases and, therefore, the sensitive measurement of ROS is of great interest. Here, we present a new device for the real-time monitoring of oxidative stress by measuring one of the most stable ROS, namely hydrogen peroxide (H2O2). This portable oxidative stress sensor contains the heme protein cytochrome c (cyt c) as sensing element whose spectral response enables the detection of H2O2 down to a detection limit of 40 nM. This low detection limit is achieved by introducing cyt c in a random medium, enabling multiscattering that enhances the optical trajectory through the cyt c spot. A contact microspotting technique is used to produce reproducible and reusable cyt c spots which are stable for several days. Experiments in static and microfluidic regimes, as well as numerical simulations demonstrate the suitability of the cyt c/H2O2 reaction system for the real-time sensing of the kinetics of biological processes without H2O2 depletion in the measurement chamber. As an example, we detect the release of H2O2 from the green alga Chlamydomonas reinhardtii exposed to either 180 nM functionalized CdSe/ZnS core shell quantum dots, or to 10 mg/l TiO2 nanoparticles. The continuous measurement of extracellular H2O2 by this optical sensor with high sensitivity is a promising new means for real-time cytotoxicity tests, the investigation of oxidative stress and other physiological cell processes.

Topics: Apoptosis; Biosensing Techniques; Chlamydomonas reinhardtii; Cytochromes c; Hydrogen Peroxide; Nanoparticles; Oxidative Stress; Quantum Dots; Titanium

Here we shortly report a protein device platform that is extremely stable in a buffer condition similar to human bodies. The protein device platform was fabricated by covalently attaching cytochrome c (cyt c) protein molecules to organic coupler molecules (pyridine dicarboxylic acid, PDA) that were already covalently bound to an electron-transporting substrate. A cubic nanostructured mesoporous titania film was chosen as an electron-transporting substrate because of its large-sized cubic holes (∼7 nm) and highly crystalline cubic titania walls (∼0.4 nm lattice). Binding of PDA molecules to the mesoporous titania surface was achieved by esterification reaction between carboxylic acid groups (PDA) and hydroxyl groups (titania) in the presence of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) mediator, whereas the immobilization of cyt c to the PDA coupler was carried out by the EDC-mediated amidation reaction between carboxylic acid groups (PDA) and amine groups (cyt c). Results showed that the 2,4-position isomer among several PDAs exhibited the highest oxidation and reduction peak currents. The cyt c-immobilized PDA-bound titania substrates showed stable and durable electrochemical performances upon continuous current-voltage cycling for 240 times (the final current change was less than 3%) and could detect superoxide that is a core indicator for various diseases including cancers.

Topics: Biomedical Engineering; Crystallization; Cytochromes c; Dicarboxylic Acids; Electrochemistry; Electrons; Equipment and Supplies; Humans; Nanostructures; Oxidation-Reduction; Porosity; Proteins; Pyridines; Superoxides; Surface Properties; Time Factors; Titanium

Titanium dioxide nanoparticles are increasingly being used in pharmaceutical and cosmetic products. The high aspect ratio of fibrous nanomaterials, such as carbon nanotubes and TiO(2) nanofibers (TiO(2)NFs), similar to the one used in this study makes them an attractive structural material and has attracted a lot of attention due to their possible negative health effects as suggested by their morphological similarities with asbestos. In the present study, therefore, toxicity of TiO(2)NFs was evaluated in human cervical adenocarcinoma HeLa cells. The TEM and XRD analyses showed that TiO(2)NFs used in this study are pure with uniform diameter of around 200 nm, and their length to width aspect ratio ranged between 5 and 15. Exposure of HeLa cells to TiO(2)NFs induced significant cytotoxicity even at doses as low as 2 μg/ml. The intracellular uptake of TiO(2)NFs in cells was shown by Alizarin Red S (ARS) labeled nanofibers. The mechanism of toxicity is mainly due to the induction of cellular oxidative stress, as revealed by elevated ROS levels, reduced antioxidant levels, and increased lipid peroxidation leading to apoptosis. The cell cycle analysis indicated G(2)/M cell cycle arrest in the cells exposed to TiO(2)NF. TiO(2)NFs treatment to HeLa cells resulted in increased expression of proapoptotic proteins Bax with an increase in cytosolic Cytochrome-C and inhibition of anti-apoptotic protein Bcl-2. Our results revealed the potential mechanism of cellular effects of TiO(2)NFs.

Topics: Antioxidants; Apoptosis; bcl-2-Associated X Protein; Caspase 3; Cell Cycle Checkpoints; Cell Division; Cell Line, Tumor; Cytochromes c; G2 Phase; HeLa Cells; Humans; Lipid Peroxidation; Metal Nanoparticles; Nanofibers; Oxidative Stress; Particle Size; Proto-Oncogene Proteins c-bcl-2; Reactive Oxygen Species; Titanium

The increased application of nanomaterials has raised the level of public concern regarding possible toxicities caused by exposure to nanostructures. The interactions of nanosized hydroxyapatite (HA) with cytochrome c and hemoglobin were investigated by zeta-potential, UV-vis, fluorescence and circular dichroism. The experimental results indicated that the interactions were formed via charge attraction and hydrogen bond and obeyed Langmuir adsorption isotherm. The two functional proteins bridged between HA particles to aggregate into the coralloid form, where change of the secondary structure of proteins occurred. From effects of nanosized HA, SiO(2) and TiO(2) particles on the zebrafish embryos development, they were adsorbed on the membrane surface confirmed by the electronic scanning microscopy. Nano-HA aggregated into the biggest particles around the membrane protein and then caused a little toxicity to development of zebrafish embryos. The SiO(2) particles were distributed throughout the outer surface and caused jam of membrane passage, delay of the hatching time and axial malformation. Maybe owing to the oxygen free radical activity, TiO(2) caused some serious deformity characters in the cardiovascular system.

Topics: Adsorption; Animals; Cytochromes c; Durapatite; Embryo, Nonmammalian; Embryonic Development; Hydrogen-Ion Concentration; Larva; Nanostructures; Osmolar Concentration; Protein Binding; Silicon Dioxide; Temperature; Titanium; Zebrafish; Zebrafish Proteins

Titania films having relatively uniform spherical pores were successfully fabricated using polystyrene-block-poly(ethylene oxide) (PS(n)-b-PEO(m)) diblock copolymers. Depending on the molecular weight of PS(n)-b-PEO(m), the spherical pores were varied from large mesopores (n = 40,000, m = 53,000; ∼40 nm) to macropores (n = 58,600, m = 71,000; ∼60 nm, n = 100,000, m = 150,000; ∼100 nm) in diameter. It was confirmed that the porous structures were thermally stable with crystallization of the titania frameworks. Interconnectivity between the spherical pores was reliant on the micellar arrangement of hydrophobic PS cores, while the amount of isolated pores was increased in the films prepared using low molecular weight PS(n)-b-PEO(m). The presence of such isolated pores was confirmed on the basis of adsorption experiments by using a globular hemoprotein cytochrome c (ca. 3.1 nm). Highly interconnected spherical pores, which were preferentially fabricated using high molecular weight PS(n)-b-PEO(m), were quite helpful for smooth diffusion-adsorption of bulky proteins inside the porous films.

Topics: Adsorption; Cytochromes c; Diffusion; Polyethylene Glycols; Polystyrenes; Porosity; Titanium

Increasing environmental and occupational exposures to nanoparticles (NPs) warrant deeper insight into the toxicological mechanisms induced by these materials. The present study was designed to characterize the cell death induced by carbon black (CB) and titanium dioxide (TiO2) NPs in bronchial epithelial cells (16HBE14o- cell line and primary cells) and to investigate the implicated molecular pathways.. Detailed time course studies revealed that both CB (13 nm) and TiO2(15 nm) NP exposed cells exhibit typical morphological (decreased cell size, membrane blebbing, peripheral chromatin condensation, apoptotic body formation) and biochemical (caspase activation and DNA fragmentation) features of apoptotic cell death. A decrease in mitochondrial membrane potential, activation of Bax and release of cytochrome c from mitochondria were only observed in case of CB NPs whereas lipid peroxidation, lysosomal membrane destabilization and cathepsin B release were observed during the apoptotic process induced by TiO2 NPs. Furthermore, ROS production was observed after exposure to CB and TiO2 but hydrogen peroxide (H2O2) production was only involved in apoptosis induction by CB NPs.. Both CB and TiO2 NPs induce apoptotic cell death in bronchial epithelial cells. CB NPs induce apoptosis by a ROS dependent mitochondrial pathway whereas TiO2 NPs induce cell death through lysosomal membrane destabilization and lipid peroxidation. Although the final outcome is similar (apoptosis), the molecular pathways activated by NPs differ depending upon the chemical nature of the NPs.

Topics: Apoptosis; bcl-2-Associated X Protein; Bronchi; Caspases; Cell Line; Cell Membrane; Cell Size; Cell Survival; Chromatin; Cytochromes c; DNA Fragmentation; Humans; Hydrogen Peroxide; Lipid Peroxidation; Lysosomes; Membrane Potential, Mitochondrial; Metal Nanoparticles; Mitochondria; Reactive Oxygen Species; Respiratory Mucosa; Soot; Titanium

This paper demonstrates a novel strategy for site-selective cell adhesion and in situ cultivation of living cells, integrated with real-time monitoring of cellular small biomolecules based on dual functional protein microarrays. The protein microarrays have been produced on the superhydrophobic|philic Au-TiO2 micropatterns, through further modification of L-cysteine (Cys) and followed by successive immobilization of a model protein, cytochrome c (cyt c). Experimental results have revealed that the created cyt c microarrays play dual functions: one is employed as a robust substrate for site-selective cell adhesion and in situ cultivation of living cells, because the protein microarrays exhibit high selectivity and bioaffinity toward cells, as well as long biostability under cell culture condition up to 7 days. Meanwhile, the cyt c microarrays can also serve as sensing elements for hydrogen peroxide (H2O2) due to the inherent enzymatic activity of the heme center in cyt c. Direct electron transfer of cyt c has been enhanced at the Cys-modified Au-TiO2 (Au-TiO2/Cys) microarrays, and the electrochemical behavior can be tuned by varying the width and spacing of the microband arrays. Furthermore, cyt c is stably immobilized on the Au-TiO2/Cys microarrays and maintains its enzymatic activity after confined on the microarrays. Thus, the optimized cyt c microarrays show striking analytical performance for H2O2 determination, e.g., high sensitivity and selectivity, broad linear range from 10(-9) M to 10(-2) M, low detection limit down to 2 nM, and short response time within 5 s. As a result, the excellent analytical properties of the cyt c microarrays, as well as the characteristic of the protein microarrays themselves, including high selectivity, long biostability, and good bioaffinity, opens up a method for selective in situ cultivation of cells integrated with real-time detection of signaling biomolecules such as H2O2 released from living cells, which shows potential for physiological and pathological investigations.

Topics: Cell Line, Tumor; Cysteine; Cytochromes c; Electrochemical Techniques; Gold; Humans; Hydrogen Peroxide; Protein Array Analysis; Surface Properties; Time Factors; Titanium

Porous nano-titanium dioxide (TiO(2)) particles with anatase framework were prepared by using an effective template of hydrophobic ionic liquid, i.e., N, N-bis [2-methylbutyl] imidazolium hexafluorophosphate ([PPim][PF(6)]). The nano-TiO(2) particles were characterized with TEM and BET, resulting in the distribution of the pore diameters centering at 7.3 nm and 26.2 nm, attributed to the template effect of the ionic liquid and the aggregation of the TiO(2) particles, respectively. A much improved surface area of 68.31 m(2) g(-1) and a pore volume of 0.2814 cm(3) g(-1) were obtained with respect to 15.16 m(2) g(-1) and 0.0402 cm(3) g(-1) achieved by the non-templated nano-TiO(2) counterpart. The porous nano-TiO(2) particles were used as adsorbent for selective adsorption and isolation of cytochrome c (cyt-c) at certain conditions. An adsorption efficiency of 87% was achieved for 150 microg ml(-1) cyt-c in 1.0 ml of sample solution at pH 9.0 by using 2.0 mg of the nano-TiO(2) particles, in comparison to 30% obtained by the non-templated nano-TiO(2). In addition, an adsorption capacity of 112.6 microg mg(-1) was derived for the porous nano-TiO(2) with respect to 25.1 microg mg(-1) for the normal ones. The absorbed cyt-c could be readily recovered by stripping with a 0.1 mol l(-1) Na(3)PO(4) solution, giving rise to a recovery of ca. 90%. The porous nano-TiO(2) particles have been used for the isolation of cyt-c from human whole blood, achieving satisfactory results by assay with SDS-PAGE.

Topics: Adsorption; Blood Chemical Analysis; Chemical Fractionation; Cytochromes c; Humans; Ionic Liquids; Nanoparticles; Porosity; Spectroscopy, Fourier Transform Infrared; Titanium

A simple, rapid, straightforward and washing/separation free of in-solution digestion method for microwave-assisted tryptic digestion of proteins (cytochrome c, lysozyme and myoglobin) using bare TiO(2) nanoparticles (NPs) prepared in aqueous solution to serve as multifunctional nanoprobes in electrospray ionization mass spectrometry (ESI-MS) was demonstrated. The current approach is termed as 'on particle ionization/enrichment (OPIE)' and it can be applied in ESI-MS, atmospheric pressure-matrix-assisted laser desorption/ionization mass spectrometry (AP-MALDI-MS) and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). The bare TiO(2) NPs can assist, accelerate and effectively enhance the digestion efficiency, sequence coverage and detection sensitivity of peptides for the microwave-assisted tryptic digestion of proteins in ESI-MS. The reason is attributed to the fact that proteins or partially digested proteins are easily attracted or concentrated onto the surface of TiO(2) NPs, resulting in higher efficiency of digestion reactions in the microwave experiments. Besides, the TiO(2) NPs could act as a microwave absorber to accelerate and enrich the protein fragments in a short period of time (40-60 s) from the microwave experiments in ESI-MS. Furthermore, the bare TiO(2) NPs prepared in aqueous solution exhibit high adsorption capability toward the protein fragments (peptides); thus, the OPIE approach for detecting the digested protein fragments via ESI and MALDI ionization could be achieved. The current technique is also a washing and separation-free technique for accelerating and enriching microwave-assisted tryptic digestion of proteins in the ESI-MS and MALDI-MS. It exhibits potential to be widely applied to biotechnology and proteome research in the near future.

Topics: Animals; Cadmium Compounds; Cattle; Chickens; Cytochromes c; Hot Temperature; Microwaves; Molecular Probes; Muramidase; Nanoparticles; Peptide Fragments; Quantum Dots; Spectrometry, Mass, Electrospray Ionization; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Sulfides; Titanium; Trypsin

The high conductive TiO(2) nanoneedles film is first employed as a support matrix for immobilizing model enzyme, cytochrome c (cyt c) to facilitate the electron transfer between redox enzymes and electrodes. Reversible and direct electron transfer of cyt c is successfully achieved at the nanostructured TiO(2) surface with the redox formal potential (E(0)') of 108.0 +/- 1.9 mV versus Ag|AgCl and heterogeneous electron transfer rate constant (k(s)) of 13.8 +/- 2.1 s(-1). Experimental data indicate that cyt c is stably immobilized onto the TiO(2) nanoneedles film and maintains inherent enzymatic activity toward H(2)O(2). On the basis of these results, the cyt c-TiO(2) nanocomposits film is capable of sensing H(2)O(2) at a suitable potential, 0.0 V (vs Ag|AgCl), where not only common anodic interferences like ascorbic acid, uric acid, 3,4-dihydroxyphenylacetic acid but also a cathodic interference, O(2), are effectively avoided. Besides high selectivity, the present biosensor for H(2)O(2) shows broad dynamic range and low detection limit. These remarkable analytical advantages, as well as the characteristic of TiO(2) nanoneedles film such as high conductivity, biocompatibility, and facile ability to miniaturize establishes a novel approach to detection of extracellular H(2)O(2) released from human liver cancer cells.

Topics: Biosensing Techniques; Cell Line, Tumor; Cytochromes c; Electrochemistry; Electrodes; Electron Transport; Extracellular Space; Humans; Hydrogen Peroxide; Linear Models; Liver Neoplasms; Nanostructures; Reproducibility of Results; Sensitivity and Specificity; Spectrophotometry, Ultraviolet; Surface Properties; Titanium

This paper demonstrates a novel approach for developing the analytical performance of electrochemical biosensors in which hydrogen peroxide (H(2)O(2)) is selected as a model target, based on surface plasmon resonance of gold nanoparticles (Au NPs) deposited onto a TiO(2) nanoneedle film. Direct electron transfer of cytochrome c (cyt. c) is realized at Au NPs deposited onto a TiO(2) nanoneedle film (Au/TiO(2) film), and both anodic and cathodic currents of the redox reaction at the Au/TiO(2) film upon visible-light irradiation are amplified. Meanwhile, in the presence of oxidized or reduced states of cyt. c, cathodic or anodic photocurrents are generated respectively by the Au/TiO(2) film, suggesting that the amplified anodic and cathodic currents are ascribed to the visible-light excitation. The photocurrent action spectrum obtained at the Au/TiO(2) film in the presence of cyt. c is in a good agreement with the surface plasmon absorption spectrum of Au NPs deposited onto the TiO(2) film, and maximum photocurrent is also consistent with the plasmon absorption peak of Au NPs themselves. It indicates that the enhanced photocurrents generated by visible-light irradiation are attributed to the surface plasmon resonance of Au NPs. On the other hand, experimental results reveal that cyt. c is stably immobilized onto the Au/TiO(2) film and maintains inherent enzymatic activity toward H(2)O(2) even under continuous visible-light illumination. The amplified redox currents of cyt. c produced by surface plasmon resonance of Au NPs, combined with the stability and enzymatic activity of cyt. c confined on the Au/TiO(2) film even after continuous visible-light illumination, subsequently provide the enhanced analytical performance in determination of H(2)O(2). The sensitivity of the present biosensor for H(2)O(2) is 4-fold larger than that obtained without visible-light irradiation, the detection limit is achieved to be 4.5 x 10(-8) M and the dynamic detection linear range extends from 1 x 10(-7) M to 1.2 x 10(-2) M.

Topics: Animals; Cytochromes c; Electrochemistry; Gold; Horses; Metal Nanoparticles; Nanostructures; Oxidation-Reduction; Photochemistry; Sensitivity and Specificity; Surface Plasmon Resonance; Titanium

A simple route for controlling the direction of plasmon-induced photocurrents at gold nanoparticles deposited on TiO(2) films is reported for the first time that is based on the electronic state of gold nanoparticles conjugated to redox-active cytochrome c and plasmon-enhanced electron exchange.

Topics: Cytochromes c; Electrodes; Gold; Metal Nanoparticles; Oxidation-Reduction; Titanium

We demonstrate remarkably fast incorporation and high loading of cytochrome c within thin films of periodically ordered nanocrystalline TiO(2) deposited on transparent electrodes. The immobilized cytochrome c is not denaturated and it can be reversibly reduced without mediator over the time scale of a few seconds as evidenced by spectroelectrochemistry.

Topics: Cytochromes c; Electrodes; Immobilized Proteins; Metal Nanoparticles; Oxidation-Reduction; Porosity; Spectrophotometry, Ultraviolet; Titanium

Titanium dioxide (TiO(2)), a commercially important material, is used in a wide variety of products. Although TiO(2) is generally regarded as nontoxic, the cytotoxicity, pathogenicity, and carcinogenicity of TiO(2) nanoparticles have been recently recognized. The present study investigated TiO(2) nanoparticle-induced cell apoptosis and molecular mechanisms involved in this process in a mouse epidermal (JB6) cell line. Using the 3-(4,5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide (MTT) assay, TiO(2) nanoparticles were found to exhibit higher cytotoxicity than fine particles. YO-PRO-1 iodide (YP) staining demonstrated that both TiO(2) nanoparticles and fine particles induced cell death through apoptosis. The signaling pathways involved in TiO(2) particle-induced apoptosis were investigated. Western-blot analysis showed an activation of caspase-8, Bid, BAX, and caspase-3 and a decrease of Bcl-2 in JB6 cells treated with TiO(2) particles. Time-dependent poly(ADP)ribose polymerase (PARP) cleavage induced by TiO(2) nanoparticles was observed. TiO(2) particles also induced cytochrome c release from mitochondria to cytosol. Further studies demonstrated that TiO(2) nanoparticles induced significant changes in mitochondrial membrane permeability, suggesting the involvement of mitochondria in the apoptotic process. In conclusion, evidence indicated that TiO(2) nanoparticles exhibit higher cytotoxicity and apoptotic induction compared to fine particles in JB6 cells. Caspase-8/Bid and mitochondrial signaling may play a major role in TiO(2) nanoparticle-induced apoptosis involving the intrinsic mitochondrial pathway. Unraveling the complex mechanisms associated with these events may provide further insights into TiO(2) nanoparticle-induced pathogenicity and potential to induce carcinogenicity.

Topics: Animals; Apoptosis; bcl-2-Associated X Protein; BH3 Interacting Domain Death Agonist Protein; Caspase 3; Caspase 8; Cell Line; Cell Survival; Cytochromes c; Epidermal Cells; Gene Expression Regulation; Mice; Mitochondria; Mitochondrial Membranes; Nanoparticles; Necrosis; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerases; Proto-Oncogene Proteins c-bcl-2; Titanium

Hybrid protein films incorporating Cyt-c immobilized on TiO(2) films were prepared and characterised optically with UV-visible spectroscopy and electrochemically with cyclic voltammetry, and their conductivity properties were studied in detail. In addition the effects of a thin overlayer coating of a second metal oxide such as SiO(2), Al(2)O(3), ZrO(2) and MgO(2) were studied and the effects over the electrochemical properties of the hybrid working electrodes were discussed.

Topics: Cytochromes c; Electric Conductivity; Electrochemistry; Electrodes; Electron Transport; Enzymes, Immobilized; Oxides; Spectrum Analysis; Titanium

Due to the dynamic nature and low stoichiometry of protein phosphorylation, enrichment of phosphorylated peptides from proteolytic mixtures is often necessary prior to their characterization by mass spectrometry. Immobilized metal affinity chromatography (IMAC) is a popular way to enrich phosphopeptides; however, conventional IMAC lacks enough specificity for efficient phosphoproteome analysis. In this study, novel Fe 3O 4@TiO 2 microspheres with well-defined core-shell structure were prepared and developed for highly specific purification of phosphopeptides from complex peptide mixtures. The enrichment conditions were optimized using tryptic digests of beta-casein, and the high specificity of the Fe 3O 4@TiO 2 core-shell microspheres was demonstrated by effectively enriching phosphopeptides from the digest mixture of alpha-casein and beta-casein, as well as a five-protein mixture containing nonphosphoproteins (bovine serum albumin (BSA), myoglobin, cytochrome c) and phosphoproteins (ovalbumin and beta-casein). The Fe 3O 4@TiO 2 core-shell microspheres were further successfully applied for the nano-LC-MS/MS analysis of rat liver phosphoproteome, which resulted in identification of 56 phosphopeptides (65 phosphorylation sites) in mouse liver lysate in a single run, indicating the excellent performance of the Fe 3O 4@TiO 2 core-shell microspheres.

Topics: Amino Acid Sequence; Animals; Caseins; Cytochromes c; Ferric Compounds; Ferrous Compounds; Hydrogen-Ion Concentration; Iron Compounds; Liver; Microspheres; Molecular Sequence Data; Myoglobin; Ovalbumin; Phosphopeptides; Phosphoproteins; Phosphorylation; Proteomics; Rats; Serum Albumin, Bovine; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Tandem Mass Spectrometry; Titanium; Trypsin

Topics: Adsorption; Caseins; Cytochromes c; Polyethylene Glycols; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Titanium

Cytochrome c is accumulated into a film of TiO(2) nanoparticles and phytate by adsorption from an aqueous solution into the mesoporous structure. Stable voltammetric responses and high concentrations of redox protein within the TiO(2) phytate layer can be achieved. Two types of electrode systems are reported with (i) the modified TiO(2) phytate film between electrode and aqueous solution phase and (ii) the modified TiO(2) phytate film buried under a porous gold electrode ('porotrode'). The electrical conductivity of TiO(2) phytate films is measured and compared in the dry and in the wet state. Although in the dry state essentially insulating, the TiO(2) phytate film turns into an electrical conductor (with approximately 4 Omega cm specific resistivity assuming ohmic behaviour) when immersed in aqueous 0.1 M phosphate buffer solution at pH 7. The redox protein cytochrome c is therefore directly connected to the electrode via diffusion and migration of electrons in the three dimensional mesoporous TiO(2) phytate host structure. Electron transfer from cytochrome c to TiO(2) is proposed to be the rate-determining step for this conduction mechanism.

Topics: Cytochromes c; Electric Conductivity; Electrochemistry; Electrodes; Membranes, Artificial; Oxidation-Reduction; Phytic Acid; Surface Properties; Titanium

The interfacing of nanostructured semiconductor photoelectrodes with redox proteins is an innovative approach to the development of artificial photosynthetic systems. In this paper, we have investigated the photoinduced electron-transfer reactions of zinc-substituted cytochrome c, ZnCyt-c, immobilized on mesoporous, nanocrystalline metal oxide electrodes. Efficient electron injection from the triplet state of ZnCyt-c is observed into TiO(2) electrodes (t(50%) approximately 100 micros) resulting in a long-lived charge-separated state (lifetime of up to 0.4 s). Further studies were undertaken as a function of electrolyte pH and metal oxide employed. Optimum yield of a long-lived charge-separated state was observed employing TiO(2) electrodes at pH 5, consistent with our previous studies of analogous dye-sensitized metal oxide electrodes. The addition of EDTA as a sacrificial electron donor to the electrolyte resulted in efficient photogeneration of molecular hydrogen, with a quantum yield per one absorbed photon of 10 +/- 5%.

Topics: Crystallization; Cytochromes c; Edetic Acid; Electrodes; Electron Transport; Enzymes, Immobilized; Hydrogen; Hydrogen-Ion Concentration; Kinetics; Metals; Nanotechnology; Oxidation-Reduction; Oxides; Protons; Titanium

This study describes a new means to conduct molecular recognition-based analysis using mass spectrometry. Taking advantage of the unique characteristic of the absorption capacity of the TiO(2) sol-gel material in the UV region, a TiO(2) sol-gel-deposited thin film was employed as the sample substrate to assist in UV laser desorption/ionization of analytes. Sol-gels are polymeric materials that are easy to prepare and modify at low temperatures. Molecularly imprinted TiO(2) sol-gels were generated for molecular recognition-based analysis. alpha-Cyclodextrin (CD) was selected as the template molecule and doped into TiO(2) in a sol-gel reaction. The molecularly imprinted TiO(2) sol was spin-coated on a glass slide, and appropriate template cavities in the TiO(2) sol-gel material were formed after the template molecules were removed. We demonstrate that this modified glass slide can be used to select alpha-CD from a sample solution containing equal amounts of alpha-, beta-, and gamma-CD (50 ppb each, 18 mL); alpha-CD was directly detected from the modified glass slide by matrix-assisted laser desorption/ionization mass spectrometry without the addition of extra matrix. This approach provides a new detection method for molecular recognition-based analysis.

Topics: alpha-Cyclodextrins; Bradykinin; Cyclodextrins; Cytochromes c; Insulin; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Spectrophotometry; Titanium

This paper describes a matrix-free method for performing desorption/ionization directly from mesoporous nanocrystalline titania sol-gel thin films, which have good absorption capacity in the ultraviolet (UV) range and can act as assisting materials during UV matrix-assisted laser desorption/ionization mass spectrometric (MALDI-MS) analysis. A high concentration of citrate buffer was added into this system to provide the proton source and to reduce the presence of alkali cation adducts of the analytes. The analyte signals appear uniformly over the whole sample deposition area. Protonated molecules (MH(+) ions) of analytes dominate the titania MALDI mass spectra. Surfactants, peptides, tryptic digest products, and small proteins with molecular weights below ca. 24 000 Da, are observed in the titania MALDI mass spectra. Detection limits for insulin are as low as ca. 2 fmol with mass resolution of ca. 660.

Topics: Bradykinin; Crystallization; Cytochromes c; Gels; Insulin; Nanotechnology; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Titanium; Trypsinogen

Transient optical spectroscopies and photocurrent action spectra are used to demonstrate photoinduced charge separation between zinc-substituted cytochrome c and a nanocrystalline TiO2 electrode.

Topics: Absorptiometry, Photon; Cytochrome c Group; Cytochromes c; Electrodes; Electrons; Enzymes, Immobilized; Porosity; Spectrometry, X-Ray Emission; Titanium