670 research outputs found

    Experimental determination of the evolution of the Bjorken integral at low Q^2

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    We extract the Bjorken integral Gamma^{p-n}_1 in the range 0.17 < Q^2 < 1.10 GeV^2 from inclusive scattering of polarized electrons by polarized protons, deuterons and 3He, for the region in which the integral is dominated by nucleon resonances. These data bridge the domains of the hadronic and partonic descriptions of the nucleon. In combination with earlier measurements at higher Q^2, we extract the non-singlet twist-4 matrix element f_2.Comment: Quoted world data updated. Minor change in some results, Minor rephrasin

    Small Angle Polarization in High Energy P--P Scattering Through Nonperturbative Chiral Symmetry Breaking

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    We show that a large anomalous contribution due to nonperturbative instanton-like gluonic field configurations to the axial charge of the proton implies high-energy spin effects in p−pp-p elastic scattering. This is the same mechanism which is responsible for anomalous baryon number violation at high energy in the standard model. We compute the proton polarization due to these effects and we show that it is proportional to the center-of-mass scattering angle with a universal (energy-independent) slope of order unity.Comment: (13 pages, 2 figures

    Knockout studies reveal an important role of <i>plasmodium</i> lipoic acid protein ligase a1 for asexual blood stage parasite survival

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    Lipoic acid (LA) is a dithiol-containing cofactor that is essential for the function of a-keto acid dehydrogenase complexes. LA acts as a reversible acyl group acceptor and 'swinging arm' during acyl-coenzyme A formation. The cofactor is post-translationally attached to the acyl-transferase subunits of the multienzyme complexes through the action of octanoyl (lipoyl): &lt;i&gt;N&lt;/i&gt;-octanoyl (lipoyl) transferase (LipB) or lipoic acid protein ligases (LplA). Remarkably, apicomplexan parasites possess LA biosynthesis as well as scavenging pathways and the two pathways are distributed between mitochondrion and a vestigial organelle, the apicoplast. The apicoplast-specific LipB is dispensable for parasite growth due to functional redundancy of the parasite's lipoic acid/octanoic acid ligases/transferases. In this study, we show that &lt;i&gt;LplA1&lt;/i&gt; plays a pivotal role during the development of the erythrocytic stages of the malaria parasite. Gene disruptions in the human malaria parasite &lt;i&gt;P.falciparum&lt;/i&gt; consistently were unsuccessful while in the rodent malaria model parasite &lt;i&gt;P. berghei&lt;/i&gt; the &lt;i&gt;LplA1&lt;/i&gt; gene locus was targeted by knock-in and knockout constructs. However, the &lt;i&gt;LplA1&lt;/i&gt; &lt;sup&gt;(-)&lt;/sup&gt; mutant could not be cloned suggesting a critical role of LplA1 for asexual parasite growth &lt;i&gt;in vitro&lt;/i&gt; and &lt;i&gt;in vivo&lt;/i&gt;. These experimental genetics data suggest that lipoylation during expansion in red blood cells largely occurs through salvage from the host erythrocytes and subsequent ligation of LA to the target proteins of the malaria parasite

    A Measurement of the Electric Form Factor of the Neutron through d⃗(e⃗,e′n)p\vec{d}(\vec{e},e'n)p at Q2=0.5Q^2 = 0.5 (GeV/c)2^2

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    We report the first measurement of the neutron electric form factor GEnG_E^n via d⃗(e⃗,e′n)p\vec{d}(\vec{e},e'n)p using a solid polarized target. GEnG_E^n was determined from the beam-target asymmetry in the scattering of longitudinally polarized electrons from polarized deuterated ammonia, 15^{15}ND3_3. The measurement was performed in Hall C at Thomas Jefferson National Accelerator Facility (TJNAF) in quasi free kinematics with the target polarization perpendicular to the momentum transfer. The electrons were detected in a magnetic spectrometer in coincidence with neutrons in a large solid angle segmented detector. We find GEn=0.04632±0.00616(stat.)±0.00341(syst.)G_E^n = 0.04632\pm0.00616 (stat.) \pm0.00341 (syst.) at Q2=0.495Q^2 = 0.495 (GeV/c)2^2.Comment: Latex2e 5 pages, 3 figure

    Coumarins and pyranocoumarins, potential novel pharmacophores for inhibition ofmeasles virus replication

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    A series of coumarin and pyranocoumarin analogues were evaluated in vitro for antiviral efficacy against measles virus (MV), strain Chicago. Of the 22 compounds tested for inhibition, six were found to have selectivity indices greater than 10. These were compounds 5-hydroxy-7-propionyloxy- 4-propylcoumarin (2a), 5,7-bis(tosyloxy)-4- propylcoumarin (7); 5-hydroxy-4-propyl-7-tosyloxy- coumarin (8); 6,6-dimethyl-9-propionyloxy-4- propyl-2H,6H-benzo[1,2-b:3,4-b′]dipyran-2-one (9); 6,6-dimethyl-9-pivaloyloxy-4-propyl-2H,6Hbenzo[ 1,2-b:3,4-b′]dipyran-2-one (10); and 7,8-cis- 10,11,12-trans-4-propyl-6,6,10,11-tetramethyl- 7,8,9-trihydroxy-2H,6H,12H-benzo[1,2-b:3,4-b′:5,6- b′′]tripyran-2-one (18). Three of the active drugs were propyl coumarin analogues (2a, 7 and 8), two were dipyranone or chromeno-coumarins (9 and 10), and one was a benzotripyranone with a coumarin nucleus (18). Some appeared to be rather specific and potent inhibitors of MV with EC50 values ranging from 0.2 to 50 μg/ml and the majority of the EC50 values being less than 5 μg/ml. The compounds inhibited an additional nine strains of MV, and in virucidal tests the drugs did not physically disrupt the virion to inhibit virus replication. The inhibitory activity for one of the compounds tested (7) was somewhat dependent on virus concentration and it was still active when added to cells up to 24 h after virus exposure. When used in combination with ribavirin, compound 7 appeared not to profoundly affect the antiviral efficacy of ribavirin or its cell-associated toxicity. However, a slightly antagonistic MVinhibitory effect was observed at the highest concentration of ribavirin used in combination with most concentrations of compound 7 tested. This and related compounds may be valuable leads in the development of a potent and selective class of MV inhibitors that could be used in future in the clinic

    Exclusive Photoproduction of Large Momentum-Transfer K and K* Mesons

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    The reactions gamma p -> K+ Lambda and gamma p -> K* Lambda are analyzed within perturbative QCD, allowing for diquarks as quasi-elementary constituents of baryons. The diquark-model parameters and the quark-diquark distribution amplitudes of proton and Lambda are taken from previous investigations of electromagnetic baryon form factors and Compton-scattering off protons. Unpolarized differential cross sections and polarization observables are computed for different choices of the K and K* distribution amplitudes. The asymptotic form of the K distribution amplitude (proportional to x1 x2) is found to provide a satisfactory description of the K photoproduction data.Comment: 32 pages, 7 figures available as tared, compressed and uuencoded PS-file
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