Investigation of quasi-realistic heterotic string models with reduced Higgs spectrum

Quasi-realistic heterotic-string models in the free fermionic formulation typically contain an anomalous U(1) that leads to supersymmetry breaking. Supersymmetry is restored by imposing F- and D-flatness on the vacuum. A three generation free fermionic standard-like model which did not admit stringent F- and D-flat directions has been presented (Cleaver et al. in Phys. Rev. D 78, 046009, 2008) and it was argued that all the moduli in that model were fixed. The particular property of that model was the reduction of the untwisted Higgs spectrum by a combination of symmetric and asymmetric internal dimension boundary conditions with respect to the internal fermions associated with the compactified dimensions. This reduction occurred without the need or presence of flat directions. In this paper we extend the analysis of free fermionic models with reduced Higgs spectrum to models with the same internal space but with modified gauge groups: SO(10) or flipped SU(5) subgroup. We show that all the models studied in this paper do admit stringent flat directions. Currently, the only examples of models that do not admit stringent flat directions are the standard-like models of Cleaver et al. (Phys. Rev. D 78, 046009, 2008). We comment on the relationship between flat directions and reduced Higgs in free fermionic models as well as the possible connection between moduli stabilization and model phenomenology.     

Crystalline Pr:SrAl12O19 waveguide laser in the visible spectral region

We fabricated waveguides in Pr:SrAl(12)O(19) crystals by direct femtosecond laser writing. The propagation losses were calculated to be as low as 0.16 dB/cm at a wavelength of 633 nm. Laser oscillation in a diode-pumped waveguide at a wavelength of 643.5 nm was realized. The output power of the waveguide laser was 28.1 mW at a slope efficiency of 8%.     

Thermal and environmental stability of poly(4-ethynyl-p-xylylene-co-p-xylylene) thin films

The aim of this paper was to test the thermal and environmental stability of poly(4-ethynyl-p-xylyleneco-p-xylylene) thin films prepared by chemical vapor deposition(CVD) and to optimize the reaction conditions of the polymer.Fourier transformed infrared spectroscopy(FTIR),thermogravimetric analysis(TGA) and fluorescence microscopy were employed to investigate the stability of the reactive polymer coatings in various environmental conditions.Chemical reactivity of the thin films were then tested by Huisgen 1,3-dipolar cycloaddition reaction(‘‘click' reaction).The alkyne functional groups on poly(4-ethynyl-p-xylylene-co-p-xylylene) thin films were found to be stable under ambient storage conditions and thermally stable up to 100 8C when annealed at 0.08 Torr in argon.We also optimized the click reaction conditions of azide-functionalized molecules with poly(4-ethynyl-p-xylylene-co-p-xylylene).The best reaction result was achieved,when copper concentration was 0.5 mmol/L,sodium ascorbate concentration to copper concentration was 5:1.In contrast,the azide concentration and temperature had no obvious effect on the surface reaction.     

Mining for bioactive scaffolds with scaffold networks: improved compound set enrichment from primary screening data

Identification of meaningful chemical patterns in the increasing amounts of high-throughput-generated bioactivity data available today is an increasingly important challenge for successful drug discovery. Herein, we present the scaffold network as a novel approach for mapping and navigation of chemical and biological space. A scaffold network represents the chemical space of a library of molecules consisting of all molecular scaffolds and smaller "parent" scaffolds generated therefrom by the pruning of rings, effectively leading to a network of common scaffold substructure relationships. This algorithm provides an extension of the scaffold tree algorithm that, instead of a network, generates a tree relationship between a heuristically rule-based selected subset of parent scaffolds. The approach was evaluated for the identification of statistically significantly active scaffolds from primary screening data for which the scaffold tree approach has already been shown to be successful. Because of the exhaustive enumeration of smaller scaffolds and the full enumeration of relationships between them, about twice as many statistically significantly active scaffolds were identified compared to the scaffold-tree-based approach. We suggest visualizing scaffold networks as islands of active scaffolds.     

Development of highly potent inhibitors of the ras-targeting human acyl protein thioesterases based on substrate similarity design

A matter of common sense: A common recognition motif consisting of a negatively charged group five to six bonds away (red) from the (thio)ester functionality (green) and a positively charged tail group ten to twelve bonds away (blue) was identified in two native acyl protein thioesterase?1 (APT1) substrates. This similarity led to the design of potent inhibitors of the Ras-depalmitoylating enzyme APT1.