Development of a novel aptamer-based sensing system using atomic force microscopy

Atomic force microscopy (AFM) can dynamically detect the adhesion or affinity force between a sample surface and a cantilever. This feature is useful as a detection method using aptamers--single-strand DNA that recognizes its target with very high affinity. The present study proposes a novel DNA aptamer-based sensing system using AFM. In this study, thrombin was chosen as the target molecule, and a DNA aptamer-based AFM sensing system based on competition was developed. The affinity force between the gold chip and the cantilever decreased as the concentration of thrombin increased. Moreover, a low detection limit of 0.2 nM was achieved. Therefore, the AFM sensing system used would be appropriate for the measurement of various chemical compounds.     

Improvement in photo-alignment efficiency of azobenzene-containing polyimide films

We have investigated the photo-induced in-plane anisotropy of the films of two different polyimides (PIs) containing azobenzene in the backbone structure (Azo-PIs), which were synthesized from the same diamine, 4, 4′-diaminoazobenzene (DAAB), and two different dianhydrides, pyromellitic dianhydride (PMDA) or oxydiphthalic anhydride (ODPA). Under the same photo-alignment condition, the in-plane anisotropy of the ODPA–DAAB PI film was significantly larger than that of the PMDA–DAAB PI film. This result shows that the photo-alignment efficiency of the former is higher than that of the latter; i.e. the photo-alignment efficiency of Azo-PI can be improved by changing the backbone structure. We believe that the observed enhancement in the photo-alignment efficiency is attributed to a lowering of the polymer chain rigidity, which is caused by introducing an ether linkage with free rotation around non-parallel bonds into the dianhydride part.     

Vitamin K2 selectively induces apoptosis of blastic cells in myelodysplastic syndrome: flow cytometric detection of apoptotic cells using APO2.7 monoclonal antibody

We have previously reported that vitamin K2 (VK2) but not VK1 has a potent apoptosis-inducing effect on freshly isolated leukemia cells from patients with various types of leukemia. By multi-color flow cytometric analysis using monoclonal antibody (mAb), APO2.7, which detects mitochondrial 7A6 antigen specifically expressed by cells undergoing apoptosis, we further investigated the apoptosis-inducing effect of VK2 on minor populations of leukemic blast cells in bone marrow from patients with myelodysplastic syndrome (MDS) and overt myeloid leukemia (post-MDS AML). Limiting dilution of CD95 (anti-Fas) mAb-treated apoptotic Jurkat cells with nonapoptotic CTB-1 cells revealed that APO2.7-positive Jurkat cells were consistently detectable by flow cytometry when present at levels of at least 5% in the CTB-1 suspension. In patient samples the gating area for leukemic clone was determined using cell surface antigen-specific mAbs conjugated with either fluorescein isothionate (FITC) or phycoerythrin (PE) and subsequently the cells stained with phycoerythrin cyanine (PE-Cy5)-conjugated APO2.7 mAb were assessed within the gating area of the leukemic clone for monitoring apoptosis. Treatment of the bone marrow mononuclear cells with 3-10 microM of VK2 (menaquinone-3, -4 and -5) in vitro potently induced apoptosis of the leukemic blast cells as compared with the untreated control cells in all 15 MDS patients tested. This effect was more prominent on blastic cells than that on mature myeloid cells such as CD34-/CD33+ gated cells. In addition, VK2 performed much less effectively on CD3-positive lymphoid cells. In contrast to VK2, VK1 did not show apoptosis-inducing activity. These data suggest that VK2 may be used for treatment of patients with MDS in blastic transformation.     

On the increase of the intensity ratio of doubly charged ions to singly charged ions for liquid gold and copper ion sources.

The reason for the increase of R21 which is defined by the intensity ratio of the doubly charged ions to the singly charged ions, was studied. Based on the conventional field evaporation theory, an increase in the electric field and/or the source temperature is considered to be attributable. We took the fact that R21 turned to decrease at the higher current regime into consideration and examined whether the change of R21 due to change in the field or temperature would finally meet the criterion for the decrease of R21. It was concluded that an increase of the source temperature may be a possible reason for the increase of R21.     

Electric dichroism studies of the bonding of Co(III) chelate with synthetic polyelectrolytes

The interactions of bis-2-(2-pyridylazo)-1-naphthol Co(III), [Co(III) (αPAN)₂⁺], with five kinds of synthetic polyelectrolytes have been studied by spectrophotometric and transient electric dichroism measurements. The polyelectrolytes were: poly(styrene sulphonic acid) (PSS); poly(acrylic acid) (PAA); poly(l-glutamic acid) (PLG); $\text{poly}\text{(N}{}^{\mathrm{<mtext>e</mtext>}}\text{,N}{}^{\mathrm{<mtext>e</mtext>}}\text{-}\text{dicarboxylmethyl-}\text{l}\text{-lysine}$ (PDCML); and poly(l-lysine) (PLL). The equilibrium constant of the reaction:

with P = polyelectrolyte residue was determined spectrophotometrically: K₁ is > 10⁷ M^?1 (PSS); (1.4 ± 0.2) × 10⁴ M^?1 (PAA); (4.0 ± 0.4) × 10³ M^?1 (PLG); (1.4 ± 0.2) × 10⁶ M^?1 (PDCML); and < 10² M^?1 (PLL) at pH 6–8. From transient electric dichroism, the angle (ψ) between the αPAN plane and the polymer axis was determined to be 65° (PSS); 52° (PAA); 55° (PLG); and 52° (PDCML). The large K₁ and ψ values for PSS are ascribed to the hydrophobic interaction between the aromatic αPAN ring and the styrene sulphonate residues of PSS. Using stopped-flow electric dichroism measurements, rapid transfer of a bound Co(III) chelate from the PDCML to PSS chains was shown to occur.     

Recent progress in the development of visible light-driven powdered photocatalysts for water splitting

Many photocatalyst materials for water splitting have been developed, particularly since the second half of the 1990s. Highly efficient water splitting on tantalate photocatalysts under UV irradiation has been achieved. Moreover, band engineering by doping, valence band formation, and synthesis of solid solutions, has led to the development of a large number of visible light-driven photocatalysts for _H2${\mathrm{H}}_2$ or _O2${\mathrm{O}}_2$ evolution from aqueous solutions containing electron donors or acceptors. Z-scheme photocatalyst systems for water splitting to _H2${\mathrm{H}}_2$ and _O2${\mathrm{O}}_2$ under visible light irradiation have been developed. This progress in the development of visible light-driven photocatalysts for water splitting is reviewed.     

Fracture toughness of silica particulate‐filled epoxy composite

The relationship between the postcuring conditions and fracture toughness on three silica particulate‐filled epoxy composites was investigated. The glass transition temperature, T_g, and the fragility parameter, m, derived from the thermo‐viscoelasticity, were used to characterize the composites, which were postcured under various conditions. The glass transition temperature and fragility both depended on both of the curing conditions and the volume fraction of silica particles. The glass transition temperature increased with the postcuring time and temperature, while the fragility generally decreased as the volume fraction increased. There was no direct correlation between the glass transition temperature and fragility. The fracture toughness depended on both the glass transition temperature and fragility. The composites with a high glass transition temperature and low fragility had high fracture toughness. These results indicate that the glass transition temperature and fragility are useful parameters for estimating the fracture toughness of the silica particulate‐filled epoxy composites. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2261–2265, 2002     

Distributed memory implementation of KLIC

This paper describes external reference management and distributed unification in a distributed implementation of a concurrent logic programming language KL1. This implementation is based on the KLIC system. KLIC has a feature calledgeneric objects that enable easy modification and extension of the system without changes in the core implementation. This distributed implementation is built upon the same core and external references are represented using generic objects. Unification operations are defined as methods of generic objects. Since creation of interprocessor reference loops cannot be avoided, we studied a new unification scheme that can cope with interprocessor reference loops. We built several experimental distributed systems that all demonstrate reasonable efficiency.     

Numerical Simulation of Solidification Process on Single Crystal Ni-Based Superalloy Investment Castings

Bridgman directional solidification of investment castings is a key technology for the production of reliable and highly efficient gas turbine blades. In this paper, a mathematical model for three-dimensional （3D） simulation of solidification process of single crystal investment castings was developed based on basic heat transfer equations. Complex heat radiation among the multiple blade castings and the furnace wall was considered in the model. Temperature distribution and temperature gradient in superalloy investment castings of single blade and multiple ones were investigated, respectively. The calculated cooling curves were compared with the experimental results and agreed well with the latter. It is indicated that the unsymmetrical temperature distribution and curved liquid-solid interface caused by the circle distribution of multiple turbine blades are probably main reasons why the stray grain and other casting defects occur in the turbine blade.