Antiapoptotic activity of argon and xenon

Although chemically non-reactive, inert noble gases may influence multiple physiological and pathological processes via hitherto uncharacterized physical effects. Here we report a cell-based detection system for assessing the effects of pre-defined gas mixtures on the induction of apoptotic cell death. In this setting, the conventional atmosphere for cell culture was substituted with gas combinations, including the same amount of oxygen (20%) and carbon dioxide (5%) but 75% helium, neon, argon, krypton, or xenon instead of nitrogen. The replacement of nitrogen with noble gases per se had no effects on the viability of cultured human osteosarcoma cells in vitro. Conversely, argon and xenon (but not helium, neon, and krypton) significantly limited cell loss induced by the broad-spectrum tyrosine kinase inhibitor staurosporine, the DNA-damaging agent mitoxantrone and several mitochondrial toxins. Such cytoprotective effects were coupled to the maintenance of mitochondrial integrity, as demonstrated by means of a mitochondrial transmembrane potential-sensitive dye and by assessing the release of cytochrome c into the cytosol. In line with this notion, argon and xenon inhibited the apoptotic activation of caspase-3, as determined by immunofluorescence microscopy coupled to automated image analysis. The antiapoptotic activity of argon and xenon may explain their clinically relevant cytoprotective effects.     

X-pinch-based neutron source

Results are presented from experimental studies of the parameters of an X-pinch-based neutron source made of 70- to 80-μm-diameter deuterated polyethylene fibers. At currents of up to 1.7 MA and a current rise time of ～150 ns, hot plasma spots were observed in the fiber crossing region. The formation of hot spots was accompanied by the generation of short soft X-ray pulses with a duration of 2–4 ns, as well as by neutron emission. The neutron energy was measured using the time-of-flight technique in four directions, at 0°, 90°, 180°, and 270° with respect to the load axis. The mean energy of the neutrons emitted along the axis towards the anode and cathode was found to be 2.0 ± 0.2 and 2.6 ± 0.1 MeV, respectively, and that of neutrons emitted in two opposite directions along the radius, 2.5 ± 0.1 and 2.4 ± 0.1 MeV. The maximum neutron yield at a current amplitude of 1.6 MA was of 10¹⁰ neutrons per shot.     

Research on Beam-Focusing Characteristics of Krypton Hall Thruster

Plasma Physics Reports - The reserves of krypton are abundant, and it has become an important high specific impulse substitute for Hall thrusters as its physical properties are closest to xenon....     

A Mathematical Formulation for 3D Quasi-Static Multibody Models of Diarthrodial Joints

This study describes a genera] set of equations for quasi-static analysis of three-dimensional multibody systems, with a particular emphasis on modeling of diarthrodial joints. The model includes articular contact, muscle forces, tendons and tendon pulleys, ligaments, and the wrapping of soft tissue structures around bone and cartilage surfaces. The general set of equations governing this problem are derived using a consistent notation for all types of links, which can be converted conveniently into efficient computer codes. The computational efficiency of the model is enhanced by the use of analytical Jacobians, particularly in the analysis of articular surface contact and wrapping of soft tissue structures around bone and cartilage surfaces. The usefulness of the multibody model is demonstrated by modeling the patellofemoral joint of six cadaver knees, using cadaver-specific data for the articular surface and bone geometries, as well as tendon and ligament insertions and muscle lines of actions. Good accuracy was observed when comparing the model patellar kinematic predictions to experimental data (mean ± stand, dev. error in translation: 0.63 ± 1.19 mm, 0.10 ± 0.71 mm, -0.29 ± 0.84 mm along medial, proximal, and anterior directions, respectively; in rotation: -1.41 ± 1.71°, 0.27 ±2.38°, -1.13 ± 1.83° in flexion, tilt and rotation, respectively). The accuracy which can be achieved with this type of model, and the computational efficiency of the algorithm employed in this study may serve in many applications such as computer-aided surgical planning, and real-time computer-assisted surgery in the operating room.     

Exploring hydrophobic sites in proteins with xenon or krypton

X-ray diffraction is used to study the binding of xenon and krypton to a variety of crystallised proteins: porcine pancreatic elastase; subtilisin Carlsberg from Bacillus licheniformis; cutinase from Fusarium solani; collagenase from Hypoderma lineatum; hen egg lysozyme, the lipoamide dehydrogenase domain from the outer membrane protein P64k from Neisseria meningitidis; urate-oxidase from Aspergillus flavus, mosquitocidal δ-endotoxin CytB from Bacillus thuringiensis and the ligand-binding domain of the human nuclear retinoid-X receptor RXR-α. Under gas pressures ranging from 8 to 20 bar, xenon is able to bind to discrete sites in hydrophobic cavities, ligand and substrate binding pockets, and into the pore of channel-like structures. These xenon complexes can be used to map hydrophobic sites in proteins, or as heavy-atom derivatives in the isomorphous replacement method of structure determination. Proteins 30:61–73, 1998. © 1998 Wiley-Liss, Inc.     

Molecular simulation of volume of mixing,Helmholtz free energy of mixing and entropy of mixing in bulk fluid mixtures

We describe a kinetic Monte Carlo molecular simulation procedure to calculate the Helmholtz free energy, the entropy and the chemical potentials of all components in a bulk fluid mixture. This allows us to derive the excess properties (volume, free energy and entropy) resulting from the mixing of homogeneous fluids of pure components at constant temperature and pressure. We have chosen neon–xenon mixtures to illustrate our method because of the large difference in collision diameter and well-depth of the interaction energy. When xenon is predominant in the mixture, the volume of mixing is larger. The excess entropy of mixing correlates with the volume of mixing, since a positive excess volume enables more configurations (more possible molecular distributions). The excess thermodynamic quantities as functions of the total density were found to be insensitive to temperature. To investigate the effects of the molecular parameters, we also studied argon–nitrogen and argon–krypton mixtures. The effect of the difference in molecular parameters is in the order: argon–nitrogen < argon–krypton < neon–xenon. A large difference in the well-depth of the interaction energies results in an increase in the excess thermodynamic variables, which is in agreement with the literature McDonald IR. NpT-ensemble Monte Carlo calculations for binary liquid mixtures. Mol Phys. 1972;23(1):41–58; Singer JVL, Singer K. Monte Carlo calculation of thermodynamic properties of binary mixtures of Lennard-Jones (12-6) liquids. Mol Phys. 1972;24(2):357–390.     

Fan-precooling effect on heat strain while wearing protective clothing

This study compared heat strain during walking while wearing impermeable protective suits between fan-precooling and nonprecooling conditions. Six males engaged in 60 min of walking at a moderate speed (～2.5 km/h) in a hot environment (37 °C, 40 % relative humidity). Fanning using a fan (4.5 m/s) and spraying water over the body before wearing the suits produced significantly lower rectal temperature before the walking (37.3?±?0.1 °C vs. 37.0?±?0.1 °C, P?P?相似文献   

条背萤幼虫水生适应性形态与游泳行为研究

研究了条背萤Luciolasubstriata幼虫的形态特征及其对游泳行为的适应。形态及扫描电镜观察发现,条背萤幼虫存在二态现象。1～2龄幼虫虫体扁平,多毛。有7对呼吸鳃,分别位于腹部第1～7节。3～6龄幼虫虫体扁平呈船形,无呼吸鳃,靠气管呼吸。二者均具有扁平桨状的足、燕尾状尾节及位于尾节末端的圆柱形粘附器官。条背萤幼虫游动时身体腹面朝上,呈仰泳姿态,足向后划水。3～6龄幼虫仰泳时足共有8种摆动姿势。幼虫仰泳时足摆动1个周期所需时间为(0.611±0.16)s。腹部末端可上下左右摆动,当幼虫向前游动时,尾部上下摆动1个周期所需时间为(1.795±0.44)s。幼虫的游泳速度为(0.85±0.16)mh。仰泳中的幼虫改变方向时,头部和尾部同时向身体的一侧弯曲,当头部与尾部呈近90°时,幼虫用力将尾部伸直,此时水产生一个反作用力继续推动幼虫转向,幼虫转向的范围为0～90°。条背萤2种类型幼虫呼吸系统的不同决定着幼虫外部形态的差异及游泳行为的不同,而导致这种呼吸系统、形态及运动行为不同的原因很可能是条背萤对环境的适应性进化。     

Effect of static magnetic field on electricity production and wastewater treatment in microbial fuel cells

The effect of a magnetic field (MF) on electricity production and wastewater treatment in two-chamber microbial fuel cells (MFCs) has been investigated. Electricity production capacity could be improved by the application of a low-intensity static MF. When a MF of 50 mT was applied to MFCs, the maximum voltage, total phosphorus (TP) removal efficiency, and chemical oxygen demand (COD) removal efficiency increased from 523?±?2 to 553?±?2 mV, ～93 to ～96 %, and ～80 to >90 %, respectively, while the start-up time and coulombic efficiency decreased from 16 to 10 days and ～50 to ～43 %, respectively. The MF effects were immediate, reversible, and not long lasting, and negative effects on electricity generation and COD removal seemed to occur after the MF was removed. The start-up and voltage output were less affected by the MF direction. Nitrogen compounds in magnetic MFCs were nitrified more thoroughly; furthermore, a higher proportion of electrochemically inactive microorganisms were found in magnetic systems. TP was effectively removed by the co-effects of microbe absorption and chemical precipitation. Chemical precipitates were analyzed by a scanning electron microscope capable of energy-dispersive spectroscopy (SEM-EDS) to be a mixture of phosphate, carbonate, and hydroxyl compounds.     

Effect of xenon binding to a hydrophobic cavity on the proton pumping cycle in bacteriorhodopsin

To understand the functional role of apolar cavities in bacteriorhodopsin, a light-driven proton pump found in Halobacterium salinarum, we investigated the crystal structure in pressurized xenon or krypton. Diffraction data from the P622 crystal showed that one Xe or Kr atom binds to a preexisting hydrophobic cavity buried between helices C and D, located at the same depth from the membrane surface as Asp96, a key residue in the proton uptake pathway. The occupation fraction of Xe or Kr was calculated as approximately 0.32 at a pressure of 1 MPa. In the unphotolyzed state, the binding of Xe or Kr caused no large deformation of the cavity. However, the proton pumping cycle was greatly perturbed when an aqueous suspension of purple membrane was pressurized with xenon gas; that is, the decay of the M state was accelerated significantly (~5 times at full occupancy), while the decay of an equilibrium state of N and O was slightly decelerated. A similar but much smaller perturbation in the reaction kinetics was observed upon pressurization with krypton gas. In a glycerol/water mixture, xenon-induced acceleration of M decay became less significant in proportion to the water activity. Together with the structure of the xenon-bound protein, these observations suggest that xenon binding helps water molecules permeate into apolar cavities in the proton uptake pathway, thereby accelerating the water-mediated proton transfer from Asp96 to the Schiff base.     

DIFFERENCES IN FORAGING LOCATION OF MEXICAN AND CALIFORNIA ELEPHANT SEALS: EVIDENCE FROM STABLE ISOTOPES IN PUPS

Female northern elephant seals, Mirounga angustirostris, from Año Nuevo (AN) in central California feed offshore in mid‐latitude waters (40°–55°N). Migratory patterns and foraging locations of seals from Mexico are unknown. Rookeries on San Benitos (SB) islands in Baja California Sur, Mexico, are ～1,170 km south of AN. Although the colonies are similar in size, seals from SB begin breeding earlier and have an earlier breeding birthing peak than seals from AN. To determine if the foraging location of seals from Mexico was similar to that of seals from California, we measured δ¹³C and δ¹⁵N values in the hair of 48 suckling pups at SB and 37 from AN, assuming that their isotopic signatures reflected those of mothers' milk, their exclusive diet. The mean δ¹³C and δ¹⁵N values for SB pups (?16.1‰± 0.9‰ and 17.7‰± 0.9‰, respectively) were significantly higher than those for AN pups (?17.6‰± 0.4‰ and 15.6‰± 1.0‰, respectively). From data on environmental isotope gradients and known behavior of SB and AN populations, we hypothesize that the isotope differences are due to females in the SB colony foraging ～8° south of seals from AN. This hypothesis can be tested by deployment of satellite tags on adult females from the SB colony.     

Stereochemistry of peptides containing 1-aminocyclopentanecarboxylic acid (Acc5): Solution and solid-state conformations of Boc-Acc5-Acc5-NHMe

The conformational analysis of a protected homodipeptide of 1-aminocyclopentanecarboxylic acid (Acc⁵) has been carried out. ¹H-nmr studies establish a β-turn conformation for Boc-Acc⁵-Acc⁵-NHMe in chloroform and dimethylsulfoxide solutions involving the methylamide NH in an intramolecular hydrogen bond. Supportive evidence for the formation of an intramolecular hydrogen bond is obtained from ir studies. X-ray diffraction studies reveal a type III β-turn conformation in the solid state stabilized by a 4 → 1 hydrogen bond between the Boc CO and methylamide NH groups. The ?,ψ values for both Acc⁵ residues are close to those expected for an ideal 3₁₀-helical conformation (?? ± 60°, ψ～ ±30°).     

Poster Sessions AP02: Proteins,Amino Acids,Peptides and Metabolism. The effect of proline rich polypeptide on the interaction between activated factor X and anti‐thrombin III

The effect of the hypothalamic neurosecretory Proline Rich Polypeptide (PRP) on the interaction of human Factor Xa (Xa) with human antithrombin III (ATIII) was investigated by SDS–PAGE and Western Blot analysis. Xa runs as two bands with masses of ～51 and ～47 kDa. A fraction of the ATIII (～55 kDa) undergoes a conformational change upon interaction with Xa to run slower at ～58 kDa. Xa and ATIII form a 1° duplex complex of ～109 and ～104 kDa, a 2° duplex complex of ～99 and ～94 kDa, and a 3° duplex complex of ～66 and ～62 kDa. Additionally, a Xa degradation product (～35 kDa) is noted. Pre‐incubation of 1.5 μg of either Xa or ATIII with 8 μg PRP for 15′ at R.T., or essentially simultaneous addition of all three, increases the 2° complex upper band, 3° complex lower band, ATIII conformational change, and the Xa degradation product. It also decreases the 3° complex upper band and the native ATIII. Xa/PRP premixtures cause a decrease in unreacted Xa. ATIII/PRP premixtures produce an increase in the 1° complex lower band and a decrease in the unreacted Xa upper band. Xa/ATIII/PRP mixtures increase both bands of the 1° complex. Thus, 8 μg PRP promotes 1° complex formation as well as formation of the 2° and 3° degradation complexes. It also promotes modification of ATIII and degradation of Xa, possibly by autolysis and/or promotion of proteolysis of the 1° complex by free Xa. Data obtained indicate the role of PRP in the molecular mechanisms of blood clotting. (Supported, in part, from a grant by the Office of Sponsored Programs and Research, BGSU.)     

Optimizations of sulphide and organic modifications of the DEAMOX process

Effect of various operational parameters (pH, bicarbonate concentration, and temperature) on the efficiency of the S- and O-modifications of the DEAMOX process was studied. It was demonstrated that the optimum pH values for the S- and O-DEAMOX processes are 7.5 ± 0.05 and 8.1 ± 0.08, respectively. The optimum bicarbonate concentration for both modifications does not exceed 24 mM. The optimum temperature for the S-DEAMOX process is 35°C, and any deviation from this value has a significant impact on this process. For the O-DEAMOX process, the optimum temperature range is 25–35°C.     

Stability of niosomes with encapsulated vitamin D3 and ferrous sulfate generated using a novel supercritical carbon dioxide method

Niosomes were prepared using a novel supercritical carbon dioxide based method to simultaneously encapsulate ferrous sulfate and vitamin D₃ as hydrophilic and hydrophobic cargo, respectively. Vesicle particle size was determined to be bimodal with peak diameters of 1.44?±?0.16?μm and 7.21?±?0.64?μm, with the smaller peak comprising 98.8% of the total niosomal volume. Encapsulation efficiency of ferrous sulfate was 25.1?±?0.2% and encapsulation efficiency of vitamin D₃ was 95.9?±?1.47%. Physical stability of the produced niosomes was assessed throughout a storage period of 21 days. Niosomes showed good physical stability at 20?°C, but storage at 4?°C showed an initial burst release, indicating possible rupture of the niosomal membrane. The Korsmeyer–Peppas equation was used to model the release of ferrous sulfate over time at both storage temperatures.     

Spatial structure and ecological efficiency in the summer zooplankton of a glacial lake

In June–July of 1993 and 1995, pelagic zooplankton dynamics of aglacial lake was investigated. In those years weather conditions diffferedsubstantially. This resulted not only in a great difference in the watersurface temperature (in 1993, <17.8± 0.47 °C; in 1995, 20.4± 0.33 °C), but also in an increase in the depth of metalimnionzone in 1995 in comparison with 1993. The ecological efficiency(K_e, the ratio of secondary to primary consumer productions,was 0.28 ± 0.031 in 1993 and 0.21± 0.034 in 1995. The higherK_e was accompanied by lowering of spatial structurization,primary and secondary consumer production. This revised version was published online in July 2006 with corrections to the Cover Date.     

Fibrinogen — fibrin transformation: 2. Influence of temperature,pH and of various enzymes on the intermediate structures

Light scattering from fibrin structures, obtained by exposure of fibrinogen to thrombin, Batroxobin (Reptilase) or coagulant fraction extracted from Contortrix venom at 20 and and 37°C, show in every case that rod-like intermediates are formed in the beginning of the aggregation process. The fibrils differ in the extent of branching and in lateral aggregation. Contortrix enzyme causes the highest branching density but the lowest lateral aggregation. Thrombin and Batroxobin give almost identical results. A change of temperature from 20 to 37°C yields an increase in branching density and lateral aggregation for the fibrin structures induced by the two snake venoms. With thrombin, however, the branching density decreases with the elevated temperature while the lateral aggregation strongly increases. Mostly opaque clots are obtained, with the exception of the clots induced by thrombin at 37°C, where a fine or traslucent gel is obtained. A very low extent of branching and translucent gels are also found with thrombin at 20°C and pH 7.3 but at pH 9.5 no correlation between a preferential cleavange of fibrinopeptide B and the lateral aggregation could be detected. The opacity is discussed as being the result of inhomogeneity in both branching and lateral aggregation. A quantitative analysis of the angular dependence of the scattered light indicates that non-activated human fibrinogen exists at least in the two conformations of a long rod, L = 95 ± 5 nm, and a short rod of 47.5 ± 5 nm, with mass fractions of ～ 70 and 30%, respectively. Only the long rod conformation of the monomer is built in the fibril. The model of a pure end-to-end aggregation is shown to be unlikely and the possibility of an overlapping of the monomeric rods over a region of ～ 8 nm is discussed.     

甜菜夜蛾人工饲料及饲养技术研究

研究了人工继代繁殖甜菜夜蛾饲料配方及饲养方法 ,测定了各虫态发育历期、幼虫死亡率、化蛹率、羽化率、蛹畸形率及不同世代蛹重。采用改进的饲料配方饲养的深圳种群 ,第 2代幼虫死亡率、化蛹率、蛹畸形率、羽化率分别为 7 8% ,97 3 % ,2 7%和 93 8% ,第 2 ,5 ,9,1 2代平均单头蛹重分别为 1 1 9 7± 1 6 1 ,98 3± 1 1 4,94 3± 1 2 6和 82 4± 9 6mg,平均单雌产卵量分别为 1 1 3 7 2± 63 3 ,684 5± 5 3 7,45 6 9± 40 2和 3 91 7± 45 6粒。人工饲养的甜菜夜蛾 ,卵、幼虫、蛹、雌性成虫的发育历期分别为 2 5～3 5 ,1 0～ 1 2 5 ,7～ 8 5和 8～ 1 4天 ,完成一个世代需要 2 1～ 2 5天。     

Stability study of stavudine-loaded O-palmitoyl-anchored carbohydrate-coated liposomes

The purpose of this study was to evaluate the physicochemical stability of carbohydrate-anchored liposomes. In the present study, carbohydrate (galactose, fucose, and mannose) was palmitoylated and anchored on the surface of positively charged liposomes (PL). The stabilities of plain neutral liposomes (NL), PL, and O-palmitoyl carbohydrate-anchored liposomes were determined. The effects of storage conditions (4°C±2°C, 25°C±2°C/60%±5% relative humidity [RH], or 40°C±2°C/75%±5% RH for a period of 10, 20, and 30 days) were observed on the vesicle size, shape, zeta potential, drug content, and in vitro ligand agglutination assay by keeping the liposomal formulations in sealed ambercolored vials (10-mL capacity) after flushing with nitrogen. The stability of liposomal formulations was found to be temperature dependent. All the liposomal formulations were found to be stable at 4°C±2°C up to 1 month. Storage at 25°C±2°C/60%±5% RH and 40°C±2°C/75%±5% RH adversely affected uncoated liposomal formulations. Carbohydrate coating of the liposomes could enhance the stability of liposomes at 25°C±2°C/60%±5% RH and 40°C±2°C/75%±5% RH. Published: May 18, 2007