75 research outputs found

    The Momentum Kernel of Gauge and Gravity Theories

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    We derive an explicit formula for factorizing an nn-point closed string amplitude into open string amplitudes. Our results are phrased in terms of a momentum kernel which in the limit of infinite string tension reduces to the corresponding field theory kernel. The same momentum kernel encodes the monodromy relations which lead to the minimal basis of color-ordered amplitudes in Yang-Mills theory. There are interesting consequences of the momentum kernel pertaining to soft limits of amplitudes. We also comment on surprising links between gravity and certain combinations of kinematic and color factors in gauge theory.Comment: 19 pages, 1 figur

    Monodromy--like Relations for Finite Loop Amplitudes

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    We investigate the existence of relations for finite one-loop amplitudes in Yang-Mills theory. Using a diagrammatic formalism and a remarkable connection between tree and loop level, we deduce sequences of amplitude relations for any number of external legs.Comment: 24 pages, 6 figures, v2 typos corrected, reference adde

    The Complete KLT-Map Between Gravity and Gauge Theories

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    We present the complete map of any pair of super Yang-Mills theories to supergravity theories as dictated by the KLT relations in four dimensions. Symmetries and the full set of associated vanishing identities are derived. A graphical method is introduced which simplifies counting of states, and helps in identifying the relevant set of symmetries.Comment: 41 pages, 16 figures, published version, typos corrected, references adde

    Improvement of catalytic performance of lignin peroxidase for the enhanced degradation of lignocellulose biomass based on the imbedded electron-relay in long-range electron transfer route

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    Background: Although lignin peroxidase is claimed as a key enzyme in enzyme-catalyzed lignin degradation, in vitro enzymatic degradation of lignin was not easily observed in lab-scale experiments. It implies that other factors may hinder the enzymatic degradation of lignin. Irreversible interaction between phenolic compound and lignin peroxidase was hypothesized when active enzyme could not be recovered after the reaction with degradation product (guaiacol) of lignin phenolic dimer. Results: In the study of lignin peroxidase isozyme H8 from white-rot fungi Phanerochaete chrysosporium (LiPH8), W251 site was revealed to make the covalent coupling with one moiety of monolignolic radical (guaiacol radical) by LC-MS/MS analysis. Hypothetical electron-relay containing W251 residue was newly suggested based on the observation of repressed radical coupling and remarkably lower electron transfer rate for W215A mutant. Furthermore, the retardation of the suicidal radical coupling between the W251 residue and the monolignolic radical was attempted by supplementing the acidic microenvironment around the W251 residue to engineer radical-robust LiPH8. Among many mutants, mutant A242D showed exceptional catalytic performances by yielding 21.1- and 4.9-fold higher increases of k(cat) and k(cat)/K-M values, respectively, in the oxidation of non-phenolic model lignin dimer. Conclusions: A mechanism-based suicide inhibition of LiPH8 by phenolic compounds was firstly revealed and investigated in this work. Radical-robust LiPH8 was also successfully engineered by manipulating the transient radical state of radical-susceptible electron-relay. Radical-robust LiPH8 will play an essential role in degradation of lignin, which will be consequently linked with improved production of sugars from lignocellulose biomass.open

    BCJ Relation of Color Scalar Theory and KLT Relation of Gauge Theory

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    We present a field theoretical proof of the conjectured KLT relation which states that the full tree-level scattering amplitude of gluons can be written as a product of color-ordered amplitude of gluons and color-ordered amplitude of scalars with only cubic vertex. To give a proof we establish the KK relation and BCJ relation of color-ordered scalar amplitude using BCFW recursion relation with nonzero boundary contributions. As a byproduct, an off-shell version of fundamental BCJ relation is proved, which plays an important role in our work.Comment: 26 pages, 9 figure

    Plasmodium falciparum Choline Kinase Inhibition Leads to a Major Decrease in Phosphatidylethanolamine Causing Parasite Death

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    This work was supported by Agencia Aragonesa para la Investigación y Desarrollo (ARAID), Ministerio de Economía y Competitividad (CTQ2013-44367-C2-2-P to R.H.-G.) and Diputación General de Aragón (DGA; B89 to R.H.-G.) and the EU Seventh Framework Programme (2007–2013) under BioStruct-X (grant agreement 283570 and BIOSTRUCTX 5186, to R.H.-G.). T.K.S. was supported by the Wellcome Trust grant 093228 and European Community’s Seventh Framework Programme under grant agreement No. 602773 (Project KINDRED).Malaria is a life-threatening disease caused by different species of the protozoan parasite Plasmodium, with P. falciparum being the deadliest. Increasing parasitic resistance to existing antimalarials makes the necessity of novel avenues to treat this disease an urgent priority. The enzymes responsible for the synthesis of phosphatidylcholine and phosphatidylethanolamine are attractive drug targets to treat malaria as their selective inhibition leads to an arrest of the parasite’s growth and cures malaria in a mouse model. We present here a detailed study that reveals a mode of action for two P. falciparum choline kinase inhibitors both in vitro and in vivo. The compounds present distinct binding modes to the choline/ethanolamine-binding site of P. falciparum choline kinase, reflecting different types of inhibition. Strikingly, these compounds primarily inhibit the ethanolamine kinase activity of the P. falciparum choline kinase, leading to a severe decrease in the phosphatidylethanolamine levels within P. falciparum, which explains the resulting growth phenotype and the parasites death. These studies provide an understanding of the mode of action, and act as a springboard for continued antimalarial development efforts selectively targeting P. falciparum choline kinase.Publisher PDFPeer reviewe

    Quantitative assessment of paravalvular regurgitation following transcatheter aortic valve replacement

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    Paravalvular aortic regurgitation (PAR) following transcatheter aortic valve implantation (TAVI) is well acknowledged. Despite improvements, echocardiographic measurement of PAR largely remains qualitative. Cardiovascular magnetic resonance (CMR) directly quantifies AR with accuracy and reproducibility. We compared CMR and transthoracic echocardiography (TTE) analysis of pre-operative and post-operative aortic regurgitation in patients undergoing both TAVI and surgical aortic valve replacement (AVR).Gareth Crouch, Phillip J Tully, Jayme Bennetts, Ajay Sinhal, Craig Bradbrook, Amy L Penhall, Carmine G De Pasquale, Robert A Baker, and Joseph B Selvanayaga
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