The real photon structure functions in massive parton model in NLO

We investigate the one-gluon-exchange ($\alpha \alpha_s$) corrections to the real photon structure functions $W_{TT}$, $W_{LT}$, $W_{TT}^{a}$ and $W_{TT}^\tau$ in the massive parton model. We employ a technique based on the Cutkosky rules and the reduction of Feynman integrals to master integrals. We show that a positivity constraint, which is derived from the Cauchy-Schwarz inequality, is satisfied among the unpolarized and polarized structure functions $W_{TT}$, $W_{TT}^a$ and $W_{TT}^\tau$ calculated up to the next-to-leading order in QCD.Comment: arXiv admin note: text overlap with arXiv:1110.262

Enzymatic one-step ring contraction for quinolone biosynthesis.

The 6,6-quinolone scaffolds on which viridicatin-type fungal alkaloids are built are frequently found in metabolites that display useful biological activities. Here we report in vitro and computational analyses leading to the discovery of a hemocyanin-like protein AsqI from the Aspergillus nidulans aspoquinolone biosynthetic pathway that forms viridicatins via a conversion of the cyclopenin-type 6,7-bicyclic system into the viridicatin-type 6,6-bicyclic core through elimination of carbon dioxide and methylamine through methyl isocyanate

Systemic production of foreign peptides on the particle surface of tobacco mosaic virus

AbstractBy using a new tobacco mosaic virus (TMV) vector [Hamamoto, H., et al. (1993) Bio/Technology, 11, 930–932], we have constructed TMV particles which present three different kinds of epitopes, two of them from influenza virus hemagglutinin (HA), and one from human immunodeficiency virus type I (HIV-I) envelope protein, on the surface of the particles. Each of these TMV particles reacted with each anti-peptide antiserum. These results suggest that this TMV vector can be used as an antigen presentation system

Enzyme-catalyzed cationic epoxide rearrangements in quinolone alkaloid biosynthesis.

Epoxides are highly useful synthons and biosynthons for the construction of complex natural products during total synthesis and biosynthesis, respectively. Among enzyme-catalyzed epoxide transformations, a reaction that is notably missing, in regard to the synthetic toolbox, is cationic rearrangement that takes place under strong acid. This is a challenging transformation for enzyme catalysis, as stabilization of the carbocation intermediate upon epoxide cleavage is required. Here, we discovered two Brønsted acid enzymes that can catalyze two unprecedented epoxide transformations in biology. PenF from the penigequinolone pathway catalyzes a cationic epoxide rearrangement under physiological conditions to generate a quaternary carbon center, while AsqO from the aspoquinolone pathway catalyzes a 3-exo-tet cyclization to forge a cyclopropane-tetrahydrofuran ring system. The discovery of these new epoxide-modifying enzymes further highlights the versatility of epoxides in complexity generation during natural product biosynthesis

Individually separated supramolecular polymer chains toward solution-processable supramolecular polymeric materials

Herein, we present a simple design concept for a monomer that affords individually separated supramolecular polymer chains. Random introduction of alkyl chains with different lengths onto a monomer prevented its supramolecular polymers from bundling, permitting the preparation of concentrated solutions of the supramolecular polymer without gelation, precipitation, or crystallization. With such a solution in hand, we succeeded in fabricating self-standing films and threads consisting of supramolecular polymers

Control of all the transitions between ground state manifolds of nitrogen vacancy centers in diamonds by applying external magnetic driving fields

We demonstrate control of all the three transitions among the ground state sublevels of NV centers by applying magnetic driving fields. To address the states of a specific NV axis among the four axes, we apply a magnetic field orthogonal to the NV axis. We control two transitions by microwave pulses and the remaining transition by radio frequency (RF) pulses. In particular, we investigate the dependence of Rabi oscillations on the frequency and intensity of the RF pulses. In addition, we perform a π pulse by the RF pulses and measured the coherence time between the ground state sublevels. Our results pave the way for control of NV centers for the realization of quantum information processing and quantum sensing

Establishment of a monoclonal antibody for human LXRα: Detection of LXRα protein expression in human macrophages

Liver X activated receptor alpha (LXRα) forms a functional dimeric nuclear receptor with RXR that regulates the metabolism of several important lipids, including cholesterol and bile acids. As compared with RXR, the LXRα protein level in the cell is low and the LXRα protein itself is very hard to detect. We have previously reported that the mRNA for LXRα is highly expressed in human cultured macrophages. In order to confirm the presence of the LXRα protein in the human macrophage, we have established a monoclonal antibody against LXRα, K-8607. The binding of mAb K-8607 to the human LXRα protein was confirmed by a wide variety of different techniques, including immunoblotting, immunohistochemistry, and electrophoretic mobility shift assay (EMSA). By immunoblotting with this antibody, the presence of native LXR protein in primary cultured human macrophage was demonstrated, as was its absence in human monocytes. This monoclonal anti-LXRα antibody should prove to be a useful tool in the analysis of the human LXRα protein

Accurate Retrieval of Atomic Structures from High-Order Harmonic Spectra

We extracted the photorecombination cross sections from the high-order harmonic spectra generated from rare gases by intense femtosecond pulses. By taking the ratio between the observed high-order harmonic spectra and recolliding electron wave packets, we successfully obtained the photorecombination cross sections