Sec13 induces genomic instability in U2OS cells

Sec13p has been known as an endoplasmic reticulum-Golgi transport protein. Recently, it has also been shown to be required for the formation of septation in the fission yeast Schizosaccharomyces pombe. In the present study, we focused on the role of a human homolog of Saccharomyces cerevisiae SEC13, Sec13 protein during mitosis in U2OS cells. We found that the expression of Sec13 was constant throughout the cell cycle, and localized to the kinetochores at metaphase during mitosis. By using green fluorescent protein technology, we observed that Sec13 is required for evasion of mitotic arrest in response to spindle damage, leading to G1-like phase and apoptotic cell death. In addition, cells expressing exogenous Sec13 showed giant nuclei compared to endogenous ones in the absence of nocodazole. These results demonstrate that Sec13 is involved in the regulation of the metaphase/anaphase transition and may be functionally associated with mitotic machinery to maintain genomic stability during mitosis.     

Synthesis of monodisperse chromium nanoparticles from the thermolysis of a Fischer carbene complex

We successfully synthesized monodisperse chromium nanoparticles from the thermolysis of a Fischer carbene complex.     

Studies on terbium activated yttrium based tantalate phosphors

Terbium activated yttrium niobium tantalate phosphors were prepared by solid-state reaction and were characterized by photoluminescence measurements, X-ray diffraction and scanning electron microscopy. Photoluminescence (PL) of Y_0.95Tb_0.05Ta_1?xNb_xO₄ phosphors (x = 0–1) are influenced by the host-lattice composition, degree of crystalline order and particle morphology and size. The effect of the morpho-structural properties on PL characteristics of Y(Ta,Nb)O₄:Tb powders is reported.     

Incommensurate structural correlations in the disordered spin-dimer state induced by X-Ray and electron irradiation in CuIr2S4

Irradiation with approximately 10 keV x rays or medium-energy electrons destroys long-range order of Ir spin dimers in CuIr2S4 while preserving the dimers locally. We find that as the order is destroyed, a new type of incommensurate structural correlations appears. This represents an intriguing example of order from disorder phenomenon, in which a previously unknown incommensurate order appears in the radiation-induced disordered state. These results suggest that two competing instabilities, one of which can be suppressed by radiation, are present in the system. Otherwise unrealized structural or electronic states can, therefore, be revealed in correlated systems by x-ray or electron irradiation.     

Coexistence of localized and delocalized surface plasmon modes in percolating metal films

Near-field intensity statistics in semicontinuous silver films over a wide range of surface coverage are investigated using near-field scanning optical microscopy. The variance of intensity fluctuations and the high-order moments of intensity enhancement exhibit local minima at the percolation threshold. This reduction in local field fluctuations results from resonant excitation of delocalized surface plasmon modes. By probing the modification of the critical indices for high-order moments of intensity enhancement caused by the delocalized states, we provide the first experimental evidence for the coexistence of localized and delocalized surface plasmon modes in percolating metal films.     

Analytic solutions of the susceptibility for Doppler-broadened two-level atoms

We derive the rigorous analytic solutions for the susceptibility of Doppler-broadened two-level atoms, valid for arbitrary laser intensities. As is usually the case with real atoms, we observe that, when the homogeneous linewidth is much narrower than the Doppler width, the real part of the susceptibility is given by the product of an imaginary error function and a Gaussian, whereas the imaginary part consists simply of a Gaussian function. By employing the analytic results, in particular, we study the effects of optical pumping and saturation on the atomic susceptibility. We also find that the real (imaginary) part of the susceptibility is weakly (strongly) dependent on such parameters as the laser intensity or the optical pumping rate. The availability of analytic solutions for the simple laser-atom interaction may provide convenient tools for its understanding as well as application to more general and realistic situations.     

Surface structure and interface dynamics of alkanethiol self-assembled monolayers on Au(111)

Scanning tunneling microscopy (STM) and high-resolution electron energy loss spectroscopy (HREELS) were used to examine the structural transitions and interface dynamics of octanethiol (OT) self-assembled monolayers (SAMs) caused by long-term storage or annealing at an elevated temperature. We found that the structural transitions of OT SAMs from the c(4 x 2) superlattice to the (6 x square root 3) superlattice resulting from long-term storage were caused by both the dynamic movement of the adsorbed sulfur atoms on several adsorption sites of the Au(111) surface and the change of molecular orientation in the ordered layer. Moreover, it was found that the chemical structure of the sulfur headgroups does not change from monomer to dimer by the temporal change of SAMs at room temperature. Contrary to the results of the long-term-stored SAMs, it was found that the annealing process did not modify either the interfacial or chemical structures of the sulfur headgroups or the two-dimensional c(4 x 2) domain structure. Our results will be very useful for a better understanding of the interface dynamics and stability of sulfur atoms in alkanethiol SAMs on Au(111) surfaces.     

Synthesis of brominated directly fused diporphyrins through gold(III)-mediated oxidation

Highly efficient synthesis of meso,meso-dibromo doubly and triply fused diporphyrins has been achieved through a powerful oxidative coupling mediated by AuCl3-AgOTf combination. In addition, palladium-catalyzed debromination of meso-bromoporphyrins has been developed. This debromination protocol enables employment of bromine as a protecting group for the reactive meso-position of porphyrins.     

Development of New Atom Transfer Radical Polymerization System by Iron (III)‐Metal Salts Without Using any External Initiator and Reducing Agent

Atom transfer radical polymerization (ATRP) catalyzed by high oxidation state metal salts of FeX₃ is developed for the first time in the absence of both external initiator and reducing agent. Methyl methacrylate (MMA) and styrene are polymerized successfully using FeX₃/Phosphorous ligands with well‐controlled molecular weight distributions (=1.5). The molecular weight of the polymers increases with monomer consumption with the progress of time and the polymerization behaviors show a decent ATRP trend. Activators and initiators are suggested to generate in situ by the addition reaction of MMA and one equivalent of FeX₃. The PMMA synthesized from without‐initiator system is characterized by ¹H, ¹³C and DEPT (distortionless enhancement by polarization transfer nuclear magnetic resonance) nuclear magnetic resonance spectroscopy. Chain extension and copolymerization experiments prove the livingness of the obtained polymer.