Ultrastructural basis for the transition of cell death mode from apoptosis to necrosis in menadione-treated osteosarcoma 143B cells

Time-dependent ultrastructural changes of menadione-treated human osteosarcoma 143B cells were correlated with those in their stainability to Annexin V and propidium iodide (PI). Populations of both apoptotic (Annexin V(+)/PI(-)) and necrotic (Annexin V(+)/PI(+)) cells, judged by flow cytometry, began to increase at 2 h after menadione treatment. The former reached a maximum at 6 h followed by abrupt decreases thereafter, while the latter continued to increase. Electron microscopically, cells obtained at 6 h after the menadione treatment consisted of mixed populations of cells with typical apoptotic features and those with a mixture of apoptotic and necrotic features, while cells obtained at 8-24 h consisted exclusively of cells with a mixture of apoptotic and necrotic features. Thus, necrotic cells, as judged by flow cytometry, were in a transitional state of cell death mode from apoptosis to necrosis and are thus designated as 'intermediate cells'. Lack of apoptotic bodies, judged by flow cytometric analysis on sub-G1 nuclei and by electron microscopy in menadione-treated cells, suggested that the transition of cell death mode from apoptosis to necrosis occurred before the apoptotic processes were completed. Effects of N-acetylcysteine and Z-VAD-fmk on menadione-induced ultrastructural changes were also studied.     

Relationships between Tg and cohesive energy: 1. Dependence of Tg on the composition of copolymers

The possibility of expressing the glass transition temperature of copolymers and homopolymers with an n-alkyl side chain as a function of two parameters (cohesive energy and steric factor) is discussed. An empirical equation representing these two factors is proposed. Calculated values are in good agreement with literature data for the investigated systems.     

Role of Sulfur on the Transition from Graphite to Cementite Eutectic in Cast Iron

In the current study, an analytic solution is considered to explain the influence of sulfur on the transition from graphite to cementite eutectic in cast iron. The outcome from the current study indicates that this transition can be related to (a) the graphite nucleation potential (directly characterized by the cell count and indirectly by the nucleation coefficients; (b) the eutectic graphite growth rate coefficient; (c) the temperature range between the equilibrium temperature for graphite eutectic and the formation temperature for cementite eutectic; and (d) the liquid volume fraction, after pre-eutectic austenite solidification. In addition, the absolute and the relative chilling tendencies, as well as critical cooling rates including the chill width of the cast iron can be predicted from the current study. The analytic model was experimentally verified for castings with various sulfur contents. It is found that the main role of sulfur on the transition from graphite to cementite eutectic is through its effect on lowering the growth coefficient, and hence, the graphite eutectic growth rate. In addition, it is found that with the increasing sulfur content, the critical cooling rate is significantly reduced, thus increasing the absolute and the relative chilling tendency values, including the chill width.     

The second evolution of ionic liquids: from solvents and separations to advanced materials--energetic examples from the ionic liquid cookbook

In this Account of the small portion of the recent research in ionic liquids (ILs) by the Rogers Group, we fast forward through the first evolution of IL research, where ILs were studied for their unique set of physical properties and the resulting potential for tunable "green solvents", to the second evolution of ILs, where the tunability of the cation and anion independently offers almost unlimited access to targeted combinations of physical and chemical properties. This approach is demonstrated here with the field of energetic ionic liquids (EILs), which utilizes this design flexibility to find safe synthetic routes to ILs with high energy content and targeted physical properties.     

Bivalent peptides as models for multimeric targets of PDZ domains

PDZ domains are among the most common modules in eukaryotic, including human, genomes. They are found exclusively in large, multidomain cytosolic proteins--often with other domains that belong to a variety of families--and are involved in a plethora of physiological and pathophysiological events. PDZ domains mediate protein-protein interactions by binding to solvent-exposed and extended C-terminal short fragments of membrane-associated proteins, such as receptors and ion channels. Most of what is known about the mechanisms of target binding by PDZ domains is inferred from studies that involve isolated recombinant PDZ domains and short synthetic peptides that represent the targets. These binary systems constitute an obvious oversimplification and disregard factors such as noncanonical modes of binding and enhanced affinity due to multimeric interactions mediated by clusters and oligomers of PDZ-domain-containing proteins. We have tested whether the interaction between a dimeric form of PDZ domain that mimics a functional dimeric guanine nucleotide exchange factor, PDZ-RhoGEF (PDZ-containing RhoA-specific guanine nucleotide exchange factor) or LARG (leukemia-associated RhoA specific guanine nucleotide exchange factor), and a bivalent peptide that mimics the dimer of the plexin B receptor, could enhance the interaction between the two moieties. Peptide dimerization was achieved by cross-linking the N-terminal ends of peptides attached to Wang resin with poly(ethylene glycol) spacers (30-45 Angstroms in length). The interaction of dimeric PDZ domains with dimeric peptides resulted in an up to 20-fold increase in affinity compared to the simple binary system. This is consistent with the notion that multimerization of both receptors and PDZ-containing proteins might constitute an important regulatory mechanism.     

Dual-polymer flocculation with unmodified and ultrasonically conditioned flocculant

Dual-polymer flocculation with unmodified and ultrasonically conditioned flocculant is presented in this paper. In the experiments two types of suspensions, i.e. chalk dust and kaolin clay in RO water were investigated. In the former case the bridging mechanism was expected whereas in the latter case charge neutralization and charge patching mechanisms should be dominant. The measurements were carried out in a laboratory setup for on-line particle size distribution (PSD) analysis consisting of stirred vessel with turbine mixer, laser particle size analyzer Fritsch Analysette 22 and peristaltic pump. The flocculation kinetics is described in terms of PSD and mean particle diameter change in time. Authors proved that ultrasonic conditioning may be an effective alternative for a dual-polymer flocculation where two different flocculants are used. In some cases the mechanical strength of flocs, created by combination of unmodified and conditioned polymers, was improved which resulted in reduction of time needed to achieve the steady state of the system.     

Chemical structure of poly(β‐cyclodextrin‐co‐citric acid)

We synthesized water‐insoluble polymers, poly(β‐cyclodextrin‐co‐citric acid)s, by heating a mixture of citric acid, cyclodextrin (CD), and Na₂HPO₄ as a catalyst with a 6 : 1 : 2 molar ratio at 160, 170, and 180°C for 10 and 20 min. The chemical composition of the polyesters was determined by high pressure liquid chromatography (HPLC) analysis of the polymer hydrolysates. The crosslinking mechanisms and thermal degradation of the polymers were also investigated. The polyesters contained 30–35% citric acid, 1–4% unsaturated carboxylic acids (i.e., itaconic, cis‐aconitic, trans‐aconitic, and mesaconic acids), and 60–70% CD, whereas about 40% of them were able to form inclusion complexes. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Investigation of the thermal and magnetic properties of Fe61Co10Zr2 Fe61Co10Zr2.5Hf2.5Me2W2B20 (Me = Y, Nb, W, Ti, Mo, Ni) bulk amorphous alloys obtained by an induction suction method

The microstructure, magnetic properties and thermal stability of Fe₆₁Co₁₀Zr_2.5Hf_2.5Me₂W₂B₂₀ (Me = Y, Nb, W, Ti, Mo, Ni) alloys were investigated. The samples were obtained by an induction suction method as 0.5 mm thickness plates. The microstructure was examined using X-ray diffraction and Mössbauer spectroscopy. It was shown that the investigated samples have amorphous structure throughout the volumes of the samples. The magnetic properties were measured using a Vibrating Sample Magnetometer. The investigated alloys are soft magnetic materials with low coercivity field (from 5.8 A/m to 54 A/m) and high saturation of the magnetization (from 0.87 T to 1.26 T). The studies of thermal stability were performed using a differential scanning calorimeter. It was shown that the addition of respective atoms led to changes of Curie temperature in the range from 497 to 587 K, depending on the composition of the alloys.