Immobilization of surface non-affinitive protein onto a metal surface by an external electric field

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Tuning of ferrimagnetic nature and hyperfine interaction of Ni2+ doped cobalt ferrite nanoparticles for power transformer applications

Ferrites may contain single domain particles which gets converted into super-paramagnetic state near critical size. To explore the existence of these characteristic feature of ferrites, we have performed magnetization(M-H loop) and Mössbauer spectroscopic studies of Ni²⁺ substitution effect in Co_1-xNi_xFe₂O₄ (where x?=?0, 0.25, 0.5, 0.75 and 1) nanoparticles were fabricated by solution combustion route using mixture of carbamide and glucose as fuels for the first time. As prepared samples exhibit spinel cubic structure with lattice parameters which decreases linearly with increase in Ni²⁺ concentration. The M-H loops reveals that saturation magnetization(M_s), coercive field(H_c) remanence magnetization(M_r) and magnetron number(η_B) decreases significantly with increasing Ni²⁺ substitution. The variation of saturation magnetization has been explained on the basis of Neel's molecular field theory. The coercive field(H_c) is found strongly dependent on the concentration of Ni²⁺ and decrease of coercivity suggests that the particles have single domain and exhibits superparamagnetic behavior. The Mössbauer spectroscopy shows two ferrimagnetically relaxed Zeeman sextets distribution at room temperature. The dependence of Mössbauer parameters such as isomer shift, quadru pole splitting, line width and hyperfine magnetic field on Ni²⁺ concentration have been discussed. Hence our results suggest that synthesized materials are potential candidate for power transformer application.     

Invasion and Defense Interactions between Enzyme‐Active Liquid Coacervate Protocells and Living Cells

The design and construction of mutual interaction models between artificial microsystems and living cells have the potential to open a wide range of novel applications in biomedical and biomimetic technologies. In this study, an artificial form of invasion‐defense mutual interactions is established in a community of glucose oxidase (GOx)‐containing liquid coacervate microdroplets and living cells, which interact via enzyme‐mediated reactive oxygen species (ROS) damage. The enzyme‐containing coacervate microdroplets, formed via liquid–liquid phase separation, act as invader protocells to electrostatically bind with the host HepG2 cell, resulting in assimilation. Subsequently, the glucose oxidation in the liquid coacervates initiates the generation of H₂O₂, which serves as an ROS resource to block cell proliferation. As a defense strategy, introduction of catalase (CAT) into the host cells is exploited to resist the ROS damage. CAT‐mediated decomposition of H₂O₂ leads to the ROS scavenging and results in the recovery of cell viability. The results obtained in the current study highlight the remarkable opportunities for the development of mutual interacting communities on the interface of artificial protocells/living cells. They also provide a new approach for engineering cellular behaviors through exploiting artificial nonliving microsystems.     

Spin reorientation,normal and inverse magnetocaloric effects in heavy rare-earth iron garnets

Experiments for heavy rare-earth iron garnets Ho₃Fe₅O₁₂ and Er₃Fe₅O₁₂ show a compensation effect characterized by a near zero magnetization at 134 K and 80 K, respectively. The magnetic entropy change calculated according to the Maxwell's relation is shown to be positive and negative, indicating both normal and inverse magnetocaloric effects exist in the sample. The critical temperature (134 K for Ho₃Fe₅O₁₂, 80 K for Er₃Fe₅O₁₂) of the two types of magnetocaloric effect occurs at almost the same temperature as the compensation point. However, the compensation effect is attributed to the multiple exchange interactions among the octahedral sites Fe³⁺, the tetrahedral sites Fe³⁺ and the dodecahedral sites R³⁺, while the reversal of the magnetocaloric effect is originated from the spin reorientation. The maximum magnetic entropy change of the normal magnetocaloric effect is 4.72 J kg⁻¹ K⁻¹ for Ho₃Fe₅O₁₂ at 34 K and 4.94 J kg⁻¹ K⁻¹ for Er₃Fe₅O₁₂ at 24 K, respectively. Moreover, all the positive slopes of basic Arrott plots suggest only the second-order phase transition existing in Ho₃Fe₅O₁₂ and Er₃Fe₅O₁₂.     

应用响应曲面模型法研究丙泊酚与瑞芬太尼的最佳配伍剂量

目的:应用响应曲面模型法研究丙泊酚与瑞芬太尼合用抑制喉镜置入刺激的体动反应、循环反应及出现循环抑制副作用，评估两药相互作用方式和程度，并探索丙泊酚与瑞芬太尼最佳配伍剂量范围。方法:ASA Ⅰ-Ⅱ级患者70例，随机平行分组，选择一个预设的丙泊酚靶控输注浓度并维持丙泊酚靶浓度不变，阶梯式增加瑞芬太尼的靶浓度，评估喉镜置入刺激的体动反应、循环反应和循环抑制副作用。应用响应曲面模型分析丙泊酚与瑞芬太尼的药效学相互作用，构建最佳反应阈值范围。结果:响应曲面模型显示丙泊酚（≤9 μg/mL）和瑞芬太尼（≤10 ng/mL）联合使用在抑制喉镜置入体动反应、循环反应和产生循环抑制副作用有明显协同作用，Imax分别为2.89、5.02和2.55。将不同药效学观察指标的响应曲面相结合，构建出最佳配伍剂量范围。结论:响应曲面模型可以定性并定量的研究丙泊酚与瑞芬太尼之间的药物相互作用，并创建最佳反应阈值范围。     

超分子作用阻尼材料的动态力学模型修正

为提高飞机起落架载荷实测精度，以支柱式起落架结构为研究对象，探讨处理其载荷标定数据的工程方法。首先，对实际受载情况和单向加载工况标定数据的分析，挖掘出三向载荷、缓冲支柱压缩行程与应变码值间的数学关系，将预测的数学关系代入到多向工况的标定数据中，验证了它们的准确性;其次，根据两种标定数据回归方法，提出了对应使用的支柱式起落架载荷-应变标定方程的数学模型;最后，将两种标定方程代回到标定数据中，计算起落架三向载荷，所有反算载荷的误差均在可控范围内，表明标定方程满足精度要求。将标定方程代入实测数据中，实测曲线符合变化规律。该处理方法的应用能有力提高支柱式起落架的起飞-着陆载荷实测和载荷谱编制的准确度。     

Parallel color-coding

We present new parallelization and memory-reducing strategies for the graph-theoretic color-coding approximation technique, with applications to biological network analysis. Color-coding is a technique that gives fixed parameter tractable algorithms for several well-known NP-hard optimization problems. In this work, by efficiently parallelizing steps in color-coding, we create two new biological protein interaction network analysis tools: Fascia for subgraph counting and motif finding and FastPath for signaling pathway detection. We demonstrate considerable speedup over prior work, and the optimizations introduced in this paper can also be used for other problems where color-coding is applicable.     

Fatal Attraction: How Bacterial Adhesins Affect Host Signaling and What We Can Learn from Them

The ability of bacterial species to colonize and infect host organisms is critically dependent upon their capacity to adhere to cellular surfaces of the host. Adherence to cell surfaces is known to be essential for the activation and delivery of certain virulence factors, but can also directly affect host cell signaling to aid bacterial spread and survival. In this review we will discuss the recent advances in the field of bacterial adhesion, how we are beginning to unravel the effects adhesins have on host cell signaling, and how these changes aid the bacteria in terms of their survival and evasion of immune responses. Finally, we will highlight how the exploitation of bacterial adhesins may provide new therapeutic avenues for the treatment of a wide range of bacterial infections.