Discovery of an Allosteric Ligand Binding Site in SMYD3 Lysine Methyltransferase

SMYD3 is a multifunctional epigenetic enzyme with lysine methyltransferase activity and various interaction partners. It is implicated in the pathophysiology of cancers but with an unclear mechanism. To discover tool compounds for clarifying its biochemistry and potential as a therapeutic target, a set of drug-like compounds was screened in a biosensor-based competition assay. Diperodon was identified as an allosteric ligand; its R and S enantiomers were isolated, and their affinities to SMYD3 were determined (K_D=42 and 84 μM, respectively). Co-crystallization revealed that both enantiomers bind to a previously unidentified allosteric site in the C-terminal protein binding domain, consistent with its weak inhibitory effect. No competition between diperodon and HSP90 (a known SMYD3 interaction partner) was observed although SMYD3–HSP90 binding was confirmed (K_D=13 μM). Diperodon clearly represents a novel starting point for the design of tool compounds interacting with a druggable allosteric site, suitable for the exploration of noncatalytic SMYD3 functions and therapeutics with new mechanisms of action.     

Improvements of the structural,thermal, and mechanical properties of structural adhesive with functionalized boron nitride nanoparticles

Investigations on the production and development of nanoparticle-reinforced polymer materials have been attracted attention by researchers. Various nanoparticles have been used to improve the mechanical, chemical, thermal, and physical properties of polymer matrix composites. Boron compounds come to the fore to improve the mechanical and thermal properties of polymers. In this study, mechanical, thermal, and structural properties of structural adhesive have been examined by adding nano hexagonal boron nitride (h-BN) to epoxy matrix at different percentages (0.5, 1, 2, 3, 4, and 5%). For this purpose, nano h-BN particles were functionalized with 3-aminopropyltriethoxysilane (APTES) to disperse the h-BN nanoparticles homogeneously in epoxy matrix and to form a strong bond at the matrix interface. Two-component structural epoxy adhesive was modified by using functionalized h-BN nanoparticles. The structural and thermal properties of the modified adhesives were investigated by scanning electron microscopy and energy dispersion X-ray spectroscopy, Fourier transform infrared spectroscopy, differential scanning calorimetry, and thermogravimetric analysis techniques. Tensile test and dynamic mechanical analysis were performed to determine the mechanical properties of the adhesives. When the results obtained from analysis were examined, it was seen that the nano h-BN particles functionalized with APTES were homogeneously dispersed in the epoxy matrix and formed a strong bond. In addition that, it was concluded from the experimental results that the thermal and mechanical properties of adhesives were improved by adding functionalized nano h-BN particles into epoxy at different ratios.     

Structural,thermal, and mechanical properties of silanized boron carbide doped epoxy nanocomposites

In the presented study, the structural, thermal, and mechanical properties of the nanocomposites were investigated by doping silanized hexagonal boron carbide (h-B₄C) nanoparticles in varying proportions (0.5%, 1%, 2%, 3%, 4%, and 5%) into the epoxy resin by weight. For this purpose, the surfaces of h-B₄C nanoparticles were silanized by using 3-(glycidyloxypropyl) trimethoxysilane (GPS) to improve adhesion between h-B₄C nanoparticles and epoxy matrix. Then, the silanized nanoparticles were added to the resin by ultrasonication and mechanical stirring techniques to produce nanocomposites. The bond structure differences of silanized B₄C nanoparticles (s-B₄C) and nanoparticle doped composites were investigated by using Fourier transform infrared spectroscopy. Scanning electron microscopy and energy dispersion X-ray spectroscopy (SEM-EDS) technique was used to examine the distribution of nanoparticles in the modified nanocomposites. Differential scanning calorimetry and thermogravimetric analysis techniques were used to determine the thermal properties of the neat and s-B₄C doped nanocomposites. The tensile test and dynamic mechanical analysis were performed to determine the mechanical properties. When the experimental results were examined, changes in the bonding structure of the s-B₄C nanoparticles doped nanocomposites and significant improvements in the mechanical and thermal properties were observed. The optimum doping ratio was determined as 2% by weight. At this doping ratio, the T_g, tensile strength and storage modulus increased approximately 18%, 35%, and 44% compared to the neat composite, respectively.     

On the pitting corrosion resistance of nitrogen alloyed cold worked austenitic stainless steels

Pitting corrosion studies were carried out on cold worked (5%, 10%, 15%, 20%, 30% and 40%) nitrogen-bearing (0.05%, 0.1% and 0.22% N) type 316L austenitic stainless steels in neutral chloride medium. Potentiodynamic anodic polarisation study revealed that cold working up to 20% enhanced the pitting resistance, and thereafter a sudden decrease in pitting resistance was noticed at 30% and 40% cold working. Increase in nitrogen content was beneficial up to 20% cold work in improving the pitting corrosion resistance, beyond which it had a detrimental effect at 30% and 40% cold working. The role of nitrogen in influencing the deformation band width and dislocation configuration is explained based on the results of transmission electron microscopy investigations. Scanning electron microscopy observation of the pitted specimens indicated decreasing size and increasing density of pits, along the deformation bands with increasing nitrogen for 40% cold worked specimens. The macrohardness values increased as the cold working increased from 0% to 40%. X-ray diffraction studies revealed the increased peak broadening of austenite peak {0 2 2} with increase in cold working. The relationship between pitting corrosion and deformation structures with respect to nitrogen addition and cold working is discussed.     

Excimer Laser Micro Texturing of Cold Forging Tool Surfaces - Influence on Tool Life

In bulk metal forming the tribological state is significantly dependent on the surface topography of tool and workpiece. To provide the process with an improved tribological behaviour in some cases the billet's surface is prepared by shot blasting. Micro texturing of the tool surface provides an additional opportunity to optimise the frictional conditions.This paper deals with the investigation of micro texturing of the surface of TiN-coated tools with regard to their tribological behaviour in the field of cold forging. The micro textures are applied by excimer laser radiation. Tool life investigations in an industrial press shop yield that the tool surface can be improved significantly leading to higher tool life.     

K_(1.3)—Free图成为哈米顿的一个邻域并条件

在本文中,我们给出下列定理:设G为阶是n≥3的2—连通,K_(13)—free图且满足NC(G)≥n—δ—2。则G为哈米顿的,这里NC(G)=min{|N(u)N(v)|E}。     

Anisotropy of the electric transport properties of decagonal Al–Cu–Co(Fe) quasicrystals

The method of growth from a melt solution was used to obtain iron-alloyed (0.08 at %) Al–Cu–Co single crystals with a decagonal symmetry. The temperature dependences of the electrical resistivity in magnetic fields of 0–18 T were measured using samples oriented in the periodic direction (ρ_p(T)) and in the quasi-periodic plane (ρ_q(T)). A strong anisotropy of the resistivity was observed; the ρ_p(T) curve is linear, whereas the ρ_q(T) curve is approximated well by a second-order polynomial. A strong anisotropy of the magnetoresistance was also observed; a positive magnetoresistance Δρ/ρ ~ 10^–3 for the current flowing in the quasiperiodic plane; and a weak (close to zero) negative magnetoresistance for the current flowing along the periodic direction.     

Oxidation Behavior of the CrMnFeCoNi High-Entropy Alloy

Oxidation of the Cr₂₀Mn₂₀Fe₂₀Co₂₀Ni₂₀ (at%) high-entropy alloy (HEA) was investigated at 500–900 °C in laboratory air. At 600 °C the oxide was mainly Mn₂O₃ with a thin inner Cr₂O₃ layer; at 700 and 800 °C it was mainly Mn₂O₃ with some Cr enrichment; at 900 °C it was Mn₃O₄. The oxidation rate was initially linear but became parabolic at longer times with an activation energy of 130 kJ/mol, comparable to that of Mn diffusion in Mn oxides but much lower than that for sluggish diffusion of Mn in the HEA. The diffusion of Mn through the oxide is considered to be the rate-limiting process.