First Abundance Measurement of Organic Molecules in the Atmosphere of HH 212 Protostellar Disk

HH 212 is one of the well-studied protostellar systems, showing the first vertically resolved disk with a warm atmosphere around the central protostar. Here we report a detection of 9 organic molecules (including newly detected ketene, formic acid, deuterated acetonitrile, methyl formate, and ethanol) in the disk atmosphere, confirming that the disk atmosphere is, for HH 212, the chemically rich component, identified before at a lower resolution as a "hot-corino". More importantly, we report the first systematic survey and abundance measurement of organic molecules in the disk atmosphere within $\sim$ 40 au of the central protostar. The relative abundances of these molecules are similar to those in the hot corinos around other protostars and in Comet Lovejoy. These molecules can be either (i) originally formed on icy grains and then desorbed into gas phase or (ii) quickly formed in the gas phase using simpler species ejected from the dust mantles. The abundances and spatial distributions of the molecules provide strong constraints on models of their formation and transport in star formation. These molecules are expected to form even more complex organic molecules needed for life and deeper observations are needed to find them.Comment: 12 pages, 4 figure

Phase sensitivity at the Heisenberg limit in an SU(1,1) interferometer via parity detection

We theoretically investigate the phase sensitivity with parity detection on an SU(1,1) interferometer with a coherent state combined with a squeezed vacuum state. This interferometer is formed with two parametric amplifiers for beam splitting and recombination instead of beam splitters. We show that the sensitivity of estimation phase approaches Heisenberg limit and give the corresponding optimal condition. Moreover, we derive the quantum Cram\'er-Rao bound of the SU(1,1) interferometer.Comment: 9 pages, 2 figures, 3 table

Fibrin Gel as an Injectable Biodegradable Scaffold and Cell Carrier for Tissue Engineering

Due to the increasing needs for organ transplantation and a universal shortage of donated tissues, tissue engineering emerges as a useful approach to engineer functional tissues. Although different synthetic materials have been used to fabricate tissue engineering scaffolds, they have many limitations such as the biocompatibility concerns, the inability to support cell attachment, and undesirable degradation rate. Fibrin gel, a biopolymeric material, provides numerous advantages over synthetic materials in functioning as a tissue engineering scaffold and a cell carrier. Fibrin gel exhibits excellent biocompatibility, promotes cell attachment, and can degrade in a controllable manner. Additionally, fibrin gel mimics the natural blood-clotting process and self-assembles into a polymer network. The ability for fibrin to cure in situ has been exploited to develop injectable scaffolds for the repair of damaged cardiac and cartilage tissues. Additionally, fibrin gel has been utilized as a cell carrier to protect cells from the forces during the application and cell delivery processes while enhancing the cell viability and tissue regeneration. Here, we review the recent advancement in developing fibrin-based biomaterials for the development of injectable tissue engineering scaffold and cell carriers

Loop Formulas for Description Logic Programs

Description Logic Programs (dl-programs) proposed by Eiter et al. constitute an elegant yet powerful formalism for the integration of answer set programming with description logics, for the Semantic Web. In this paper, we generalize the notions of completion and loop formulas of logic programs to description logic programs and show that the answer sets of a dl-program can be precisely captured by the models of its completion and loop formulas. Furthermore, we propose a new, alternative semantics for dl-programs, called the {\em canonical answer set semantics}, which is defined by the models of completion that satisfy what are called canonical loop formulas. A desirable property of canonical answer sets is that they are free of circular justifications. Some properties of canonical answer sets are also explored.Comment: 29 pages, 1 figures (in pdf), a short version appeared in ICLP'1

Mechanism of action and resistant profile of anti-HIV-1 coumarin derivatives

Dicamphanoyl khellactone (DCK) is a coumarin derivative that can potently inhibit HIV-1 replication. DCK does not inhibit RNA-dependent DNA synthesis. However, an HIV reverse transcriptase (RT) inhibitor-resistant strain, HIV-1/RTMDR1, is resistant to DCK. Thus, it is possible that HIV-1 RT is the target of DCK. To test this possibility, DCK-resistant viruses were selected in the presence of DCK. Our results indicate that a single amino acid mutation, E138K in HIV-1 RT, is sufficient to confer DCK resistance. Interestingly, a DCK derivative, 3'R,4'R-Di-O-(-)-camphanoyl-2-ethyl-2',2'-dimethyldihydropyrano[2,3-f]chromo ne (DCP8), is effective against HIV-1/RTMDR1. However, the DCK-escape virus carrying the E138K mutation remains resistant to DCP8. Since DCK did not inhibit the RNA-dependent DNA polymerase activity of HIV-1 RT when using poly-rA or poly-rC as template, we evaluated the effect of DCK on the DNA-dependent DNA polymerase activity of HIV-1 RT. Our results indicate that DCK can inhibit the DNA-dependent DNA polymerase activity of HIV-1 RT. In conclusion, DCK is a unique HIV-1 RT inhibitor that inhibits the DNA-dependent DNA polymerase activity. In contrast, DCK did not significantly affect the RNA-dependent DNA polymerase activity when poly-rA or poly-rC was used as templates. An E138K mutation in the non-nucleoside RT inhibitors (NNRTIs) binding pocket of HIV-1 RT confers resistance to DCK and its chromone derivative, DCP8