1,367 research outputs found
Electron transfer via helical oligopeptide to laccase including chiral schiff base copper mediators
The oxygen reduction efficiency of a laccase-modified electrode was found to depend on the chirality of the oligopeptide linker used to bind the enzyme to the surface. At the same time, the electron transfer between the cathode electrode and the enzyme is improved by using a copper(II) complex with amino-acid derivative Schiff base ligand with/without azobenzene moiety as a mediator. The increased electrochemical current under both O2 and N2 proves that both the mediators are active towards the enzyme
Ionospheric conductivity dependence of dayside region-0, 1, and 2 field-aligned current systems: statistical study with DMSP-F7
The present study statistically examines the dependence of the intensities of dayside (MLT=8-12h) large-scale field-aligned currents (FACs) on the ionospheric conductance using the summary data of DMSP-F7 constructed by the procedure of Higuchi and Ohtani (2000). We have found that, in the dayside region, R1 and R0 have a higher correlation between ionospheric conductivity and FAC intensity than R2, suggesting that R0 and R1 are driven by a more voltage-like source than R2. This result is consistent with the idea that R1 and R0 are driven by the interaction between the solar wind and the open magnetospheric magnetic field. We have also found that dayside FAC intensities are latitudinally well balanced when they have a three sheet structure (R0, R1 and R2); on the other hand, for a two sheet structure (R1 and R2), the intensity of R1 is larger than that of R2, so that the net current has the polarity of R1
An Efficient Local Search for Partial Latin Square Extension Problem
A partial Latin square (PLS) is a partial assignment of n symbols to an nxn
grid such that, in each row and in each column, each symbol appears at most
once. The partial Latin square extension problem is an NP-hard problem that
asks for a largest extension of a given PLS. In this paper we propose an
efficient local search for this problem. We focus on the local search such that
the neighborhood is defined by (p,q)-swap, i.e., removing exactly p symbols and
then assigning symbols to at most q empty cells. For p in {1,2,3}, our
neighborhood search algorithm finds an improved solution or concludes that no
such solution exists in O(n^{p+1}) time. We also propose a novel swap
operation, Trellis-swap, which is a generalization of (1,q)-swap and
(2,q)-swap. Our Trellis-neighborhood search algorithm takes O(n^{3.5}) time to
do the same thing. Using these neighborhood search algorithms, we design a
prototype iterated local search algorithm and show its effectiveness in
comparison with state-of-the-art optimization solvers such as IBM ILOG CPLEX
and LocalSolver.Comment: 17 pages, 2 figure
Functional studies of signaling pathways in peri-implantation development of the mouse embryo by RNAi
BACKGROUND: Studies of gene function in the mouse have relied mainly on gene targeting via homologous recombination. However, this approach is difficult to apply in specific windows of time, and to simultaneously knock-down multiple genes. Here we report an efficient method for dsRNA-mediated gene silencing in late cleavage-stage mouse embryos that permits examination of phenotypes at post-implantation stages. RESULTS: We show that introduction of Bmp4 dsRNA into intact blastocysts by electroporation recapitulates the genetic Bmp4 null phenotype at gastrulation. It also reveals a novel role for Bmp4 in the regulation the anterior visceral endoderm specific gene expression and its positioning. We also show that RNAi can be used to simultaneously target several genes. When applied to the three murine isoforms of Dishevelled, it leads to earlier defects than previously observed in double knock-outs. These include severe delays in post-implantation development and defects in the anterior midline and neural folds at headfold stages. CONCLUSION: Our results indicate that the BMP4 signalling pathway contributes to the development of the anterior visceral endoderm, and reveal an early functional redundancy between the products of the murine Dishevelled genes. The proposed approach constitutes a powerful tool to screen the functions of genes that govern the development of the mouse embryo
Evaluation of Dynamic Cell Processes and Behavior Using Video Bioinformatics Tools
Just as body language can reveal a person’s state of well-being, dynamic changes in cell behavior and
morphology can be used to monitor processes in cultured cells. This chapter discusses how CL-Quant
software, a commercially available video bioinformatics tool, can be used to extract quantitative data on:
(1) growth/proliferation, (2) cell and colony migration, (3) reactive oxygen species (ROS) production, and
(4) neural differentiation. Protocols created using CL-Quant were used to analyze both single cells and
colonies. Time-lapse experiments in which different cell types were subjected to various chemical
exposures were done using Nikon BioStations. Proliferation rate was measured in human embryonic stem
cell colonies by quantifying colony area (pixels) and in single cells by measuring confluency (pixels).
Colony and single cell migration were studied by measuring total displacement (distance between the
starting and ending points) and total distance traveled by the colonies/cells. To quantify ROS production,
cells were pre-loaded with MitoSOX Red™, a mitochondrial ROS (superoxide) indicator, treated with
various chemicals, then total intensity of the red fluorescence was measured in each frame. Lastly, neural
stem cells were incubated in differentiation medium for 12 days, and time lapse images were collected
daily. Differentiation of neural stem cells was quantified using a protocol that detects young neurons. CLQuant
software can be used to evaluate biological processes in living cells, and the protocols developed in
this project can be applied to basic research and toxicological studies, or to monitor quality control in
culture facilities
Conceptualisation, Development, Fabrication and In Vivo Validation of a Novel Disintegration Tester for Orally Disintegrating Tablets
Disintegration time is the key critical quality attribute for a tablet classed as an Orally Disintegrating Tablet (ODT). The currently accepted in vitro testing regimen for ODTs is the standard United States Pharmacopeia (USP) test for disintegration of immediate release tablets, which requires a large volume along with repeated submergence of the dosage form within the disintegration medium. The aim of this study was to develop an in vivo relevant ODT disintegration test that mimicked the environment of the oral cavity, including lower volume of disintegration medium, with relevant temperature and humidity that represent the conditions of the mouth. The results showed that the newly developed Aston test was able to differentiate between different ODTs with small disintegration time windows, as well as between immediate release tablets and ODTs. The Aston test provided higher correlations between ODT properties and disintegration time compared to the USP test method and most significantly, resulted in a linear in vitro/in vivo correlation (IVIVC) (R 2 value of 0.98) compared with a "hockey stick" profile of the USP test. This study therefore concluded that the newly developed Aston test is an accurate, repeatable, relevant and robust test method for assessing ODT disintegration time which will provide the pharmaceutical industry and regulatory authorities across the world with a pragmatic ODT testing regime
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