High-performance absorbing boundary conditions for photonic crystalwaveguide simulations

A high-performance absorbing boundary condition is newly developed for the reduction of spurious reflections in photonic crystal (PC) waveguide simulations. The PC waveguide is terminated with a perfectly matched layer (PML) in which the original PC structure remains as is. This PC-based PML works well, compared to a conventional PML, which acts as a homogeneous absorbing medium, simulating a semi-infinite free space and to a distributed-Bragg-reflector waveguide, which was recently developed to reduce reflections from PC waveguide ends, improving a wavenumber matching condition for PC waveguide modes     

Deformation behavior and mechanical properties of braided rectangular pipes

The purpose of this study is to clarify the deformation behavior and the relationship between the braiding angle and mechanical properties for the braided rectangular pipe. Three-point bending test was performed for each specimen. Furthermore, the effect of the solid-core bar on the deformation state of the rectangular pipe was studied by finite element method (FEM). Moreover, the effect of the braiding angle on the deformation behavior in detail was investigated. The bending modulus and the bending strength for each specimen were decreased with an increase in the braiding angle. The local deformations occurred at the compression side under loading nose and decreased with an increase in stiffness properties in circumferential direction. From FEM analysis, using the aluminum solid-core bar was effective to restrain the local deformation. The difference between the bending moduli of experiments and FEM was decreased with an increase in the modulus in transverse direction.     

The Characteristic Structure of Anti‐HIV Actinohivin in Complex with Three HMTG D1 Chains of HIV‐gp120

The anti‐HIV lectin actinohivin (AH) specifically interacts with HMTG (high‐mannose‐type glycan), which is attached to the glycoprotein gp120 of HIV‐1 in a process in which the three branched mannotriose chains (D1, D2, and D3) of HMTG exhibit different binding affinities, it being estimated that that of D1 is the strongest, that of D3 is weaker, and that of D2 is undetectable. These properties have been ascribed to the stereochemical differences in linkages between the second and the third mannose residues of the three chains. In order to clarify the interaction geometry between AH and the major target D1, an X‐ray determination of the crystal structure of AH in complex with D1—which is α(1,2)mannotriose composed of three mannose (Man) residues linked together only by α(1,2) bonding—has been performed. In each of the three D1‐binding pockets of AH, two Man residues of D1 are accommodated at zones 1 and 2 in the pocket, in the same way as those found in the α(1,2)mannobiose‐bound AH crystals. However, an OMIT map shows poor densities at both ends of the two residues. This suggests the existence of positional disorder of D1 in the pocket: the two zones are each occupied by two Man residues in two different modes, with mode A involving the Man1 and Man2 residues and mode B the Man2 and Man3 residues. In each mode, D1 is stabilized by adopting a double‐bracket‐shaped conformation through C?H ??? O interactions. In mode B, however, the Man1 residue, which is the most sensitive residue to AH binding, protrudes wholly into the solvent region without contacts with AH. In mode A, in contrast, the Man3 residue interacts with the essential hydrophobic amino acid residues (Tyr and Leu conserved between the three pockets) of AH. Therefore, mode A is likely to be the one that occurs when whole HMTG is bound. In this mode, the two hydroxy groups (O3 and O4) of the Man2 residue are anchored in zone 2 by four hydrogen bonds with Asp, Asn, and Tyr residues of AH. In addition, it has been found that an isolated water molecule buried in the hydrophobic long loop bridges between Asp of AH and the hydroxy group of Man2 through hydrogen bonds. The most interesting feature is found in the interaction of the Man1 and Man3 residues with AH. All eight hydroxy groups of the two residues are completely exposed in the solvent region, whereas their hydrophobic parts make contacts with a Leu residue and two Tyr residues so that the shape of D1 and the surface of AH fit well over a wide area. These structural characteristics are potentially useful for development of AH to produce more effective antiretroviral drugs to suppress the infectious expansion of HIV/AIDS and to help expedite an end to the HIV/AIDS pandemic in the near future.     

A Cyclic KLVFF‐Derived Peptide Aggregation Inhibitor Induces the Formation of Less‐Toxic Off‐Pathway Amyloid‐β Oligomers

Inhibition of amyloid‐β (Aβ) aggregation could be a target of drug development for the treatment of currently incurable Alzheimer's disease. We previously reported that a head‐to‐tail cyclic peptide of KLVFF (cyclic‐KLVFF), a pentapeptide fragment corresponding to the Aβ16–20 region (which plays a critical role in the generating Aβ fibrils), possesses potent inhibitory activity against Aβ aggregation. Here we found that the inhibitory activity of cyclic‐KLVFF was significantly improved by incorporating an additional phenyl group at the β‐position of the Phe4 side chain (inhibitor 3 ). Biophysical and biochemical analyses revealed the rapid formation of 3 ‐embedded oligomer species when Aβ1–42 was mixed with 3 . The oligomer species is an “off‐pathway” species with low affinity for cross‐β‐sheet‐specific dye thioflavin T and oligomer‐specific A11 antibodies. The oligomer species had a sub‐nanometer height and little capability of aggregation to amyloid fibrils. Importantly, the toxicity of the oligomer species was significantly lower than that of native Aβ oligomers. These insights will be useful for further refinement of cyclic‐KLVFF‐based aggregation inhibitors.     

Prevention of Cracks in Functionally Graded SiO2‐Mo Materials Fabricated by Uniaxial Compression Casting and Pressureless Sintering

In industrial high‐intensity discharge lamps, cracks and delaminations occasionally develop at the interface between SiO₂ and the Mo foil in the seal. Here, functionally graded SiO₂‐Mo materials for use in these lamps were fabricated by uniaxial compression casting and pressureless sintering. Consequently, vertical cracks developed across the sintered body layers, and interfacial cracks developed between the 100 wt% SiO₂ and 90 wt% SiO₂‐Mo layers. Therefore, the effects of residual stress, difference in the coefficient of thermal expansion (CTE), and difference in the volume shrinkage on these cracks were investigated. Vertical cracks were suppressed when residual stress was relaxed by annealing near the annealing point of silica glass during the cooling step in the sintering process. Interfacial cracks were suppressed when the difference in the CTE of the interface between the 100 wt% SiO₂ and 90 wt% SiO₂‐Mo layers was relaxed by inserting layers of 95 wt% SiO₂‐Mo between them. Furthermore, the suppression effect became stronger when the difference in the volume shrinkage of the layers was relaxed by sintering to join the separately sintered monolayers. Thus, the development of these cracks was influenced by the residual stress, CTE, and volume shrinkage. Therefore, these cracks can be prevented by optimizing these factors.     

Convenient Synthesis of Mesoporous Aluminosilicates by Using Pre-heated Sodium Aluminosilicate Gel

Hydrothermally stable Al-MCM-48 with variety of Si/Al ratios and Al-MCM-41 with tunable pore sizes were successfully obtained from pre-heated aluminosilicate gel precursor. They showed the higher acid strength and hydrothermal stability comparing with conventional ones. Thus, this synthetic strategy offers a straightforward and convenient access to mesoporous aluminosilicates with zeolite-like acidity and stability.     

α-Synuclein and DJ-1 as Potential Biological Fluid Biomarkers for Parkinson's Disease

Parkinson's disease (PD) is the most common form of movement disorder and affects approximately 4% of the population aged over 80 years old. Currently, PD cannot be prevented or cured, and no single diagnostic biomarkers are available. Notably, recent studies suggest that two familial PD-linked molecules, α-synuclein and DJ-1, are present in cerebrospinal fluid (CSF) and that their levels may be altered during the progression of PD. In this regard, sensitive and accurate methods for evaluation of α-synuclein and DJ-1 levels in the CSF and blood have been developed, and the results suggest that the levels of both molecules are significantly decreased in the CSF in patients with PD compared with age-matched controls. Furthermore, specific detection and quantification of neurotoxic oligometric forms of α-synuclein in the blood using enzyme-linked immunosorbent assays might be expected as potential peripheral biomarkers for PD, although further validation is required. Currently, neither α-synuclein nor DJ-1 is satisfactory as a single biomarker for PD, but combinatory evaluation of these biological fluid molecules with other biomarkers and imaging techniques may provide reliable information for diagnosis of PD.