1,436 research outputs found

    Optimal design of particle dampers for structures with low first eigenfrequency under forced vibration

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    Lightweight designs are becoming increasingly important these days to reduce energy consumption and natural resources. However, a smaller weight typically causes a decrease in stiffness and non-negligible vibration amplitudes over a wide frequency range. One passive damping technique to reduce such vibrations is the use of particle dampers. Thereby containers attached to a vibrating structure or holes embedded in the vibrating structure are filled with granular material. Due to the structural vibrations, momentum is transferred to the granular material which interacts with each other. As a result, energy is dissipated by impacts and frictional phenomena between the particles. Recently, the rolling attribute of spheres has been used to design efficient particle dampers for low amplitude vibrations. As long as the container’s acceleration stays below the gravitational acceleration, this rolling effect can be used to damp horizontal vibrations efficiently. The description of the damper’s energy dissipation is accurately possible using analytical formulas which are presented here. In this presentation, the workflow for a systematic damper design is presented using the analytical formulas and validated experimentally . A good agreement between analytical and experimental measurements is achieved for an optimized damper, validating the presented approach

    Competition of Dzyaloshinskii-Moriya and higher-order exchange interactions in Rh/Fe atomic bilayers on Ir(111)

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    Using spin-polarized scanning tunneling microscopy and density functional theory we demonstrate the occurrence of a novel type of noncollinear spin structure in Rh/Fe atomic bilayers on Ir(111). We find that higher-order exchange interactions depend sensitively on the stacking sequence. For fcc-Rh/Fe/Ir(111) frustrated exchange interactions are dominant and lead to the formation of a spin spiral ground state with a period of about 1.5 nm. For hcp-Rh/Fe/Ir(111) higher-order exchange interactions favor a double-row wise antiferromagnetic or "uudd" state. However, the Dzyaloshinskii- Moriya interaction at the Fe/Ir interface leads to a small angle of about 4{\deg} between adjacent magnetic moments resulting in a canted "uudd" ground state

    A tree without leaves

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    The puzzle presented by the famous stumps of Gilboa, New York, finds a solution in the discovery of two fossil specimens that allow the entire structure of these early trees to be reconstructed

    Switching the Switch: Ligand Induced Disulfide Formation in HDAC8

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    Human histone deacetylase 8 is a well‐recognized target for T‐cell lymphoma and particularly childhood neuroblastoma. PD‐404,182 was shown to be a selective covalent inhibitor of HDAC8 that forms mixed disulfides with several cysteine residues and is also able to transform thiol groups to thiocyanates. Moreover, HDAC8 was shown to be regulated by a redox switch based on the reversible formation of a disulfide bond between cysteines Cys102_{102} and Cys153_{153}. This study on the distinct effects of PD‐404,182 on HDAC8 reveals that this compound induces the dose‐dependent formation of intramolecular disulfide bridges. Therefore, the inhibition mechanism of HDAC8 by PD‐404,182 involves both, covalent modification of thiols as well as ligand mediated disulfide formation. Moreover, this study provides a deep molecular insight into the regulation mechanism of HDAC8 involving several cysteines with graduated capability to form reversible disulfide bridges

    3‐Chloro‐5‐Substituted‐1,2,4‐Thiadiazoles (TDZs) as Selective and Efficient Protein Thiol Modifiers

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    The study of cysteine modifications has gained much attention in recent years. This includes detailed investigations in the field of redox biology with focus on numerous redox derivatives like nitrosothiols, sulfenic acids, sulfinic acids and sulfonic acids resulting from increasing oxidation, S-lipidation, and perthiols. For these studies selective and rapid blocking of free protein thiols is required to prevent disulfide rearrangement. In our attempt to find new inhibitors of human histone deacetylase 8 (HDAC8) we discovered 5-sulfonyl and 5-sulfinyl substituted 1,2,4-thiadiazoles (TDZ), which surprisingly show an outstanding reactivity against thiols in aqueous solution. Encouraged by these observations we investigated the mechanism of action in detail and show that these compounds react more specifically and faster than commonly used N-ethyl maleimide, making them superior alternatives for efficient blocking of free thiols in proteins. We show that 5-sulfonyl-TDZ can be readily applied in commonly used biotin switch assays. Using the example of human HDAC8, we demonstrate that cysteine modification by a 5-sulfonyl-TDZ is easily measurable using quantitative HPLC/ESI-QTOF-MS/MS, and allows for the simultaneous measurement of the modification kinetics of seven solvent-accessible cysteines in HDAC8
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