1,058 results on '"Engineering and Physical Sciences Research Council (UK)"'
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1052. Real-space multiple scattering theory for superconductors with impurities
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Balazs Ujfalussy, Tom G. Saunderson, James F. Annett, Martin Gradhand, Zsolt Győrgypál, Gábor Csire, Engineering and Physical Sciences Research Council (UK), National Research, Development and Innovation Office (Hungary), European Commission, Ministerio de Ciencia, Innovación y Universidades (España), Agencia Estatal de Investigación (España), and Generalitat de Catalunya
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cond-mat.supr-con ,Center of excellence ,media_common.quotation_subject ,FOS: Physical sciences ,Library science ,02 engineering and technology ,01 natural sciences ,7. Clean energy ,Superconductivity (cond-mat.supr-con) ,Condensed Matter - Strongly Correlated Electrons ,Excellence ,Political science ,Condensed Matter::Superconductivity ,0103 physical sciences ,media_common.cataloged_instance ,European union ,010306 general physics ,media_common ,Strongly Correlated Electrons (cond-mat.str-el) ,Condensed Matter - Superconductivity ,Charter ,021001 nanoscience & nanotechnology ,Multiple scattering theory ,Christian ministry ,cond-mat.str-el ,0210 nano-technology - Abstract
We implement the Bogoliubov-de Gennes (BdG) equation in real-space using the screened Korringa-Kohn-Rostoker (KKR) method. This allows us to solve, self-consistently, the superconducting state for 3D crystals including substitutional impurities with a full normal-state DFT band structure. We apply the theoretical framework to bulk Nb with impurities. Without impurities, Nb has an anisotropic gap structure with two distinct peaks around the Fermi level. In the presence of nonmagnetic impurities, those peaks are broadened due to the scattering between the two bulk superconducting gaps, however the peaks remain separated. As a second example of self-consistent real-space solutions of the BdG equations, we examine superconducting clusters embedded within a nonsuperconducting bulk metallic host. This allows us to estimate the coherence length of the superconductor and we show that, within our framework, the coherence length of the superconductor is related to the inverse of the gap size, just as in bulk BCS theory., This work was financially supported by the Centre for Doctoral Training in Condensed Matter Physics, funded by EPSRC, Grant No. EP/L015544/1. B.U. was supported by the Hungarian National Research, Development and Innovation Office under Contract No. OTKA K131938. The research reported in this paper and carried out at BME has been supported by the NRDI Fund (TKP2020 IES, Grant No. BME-IE-NAT) based on the charter of bolster issued by the NRDI Office under the auspices of the Ministry for Innovation and Technology. G.C. gratefully acknowledges support from the European Union’s Horizon 2020 research and innovation programme under the Marie-Sklodowska-Curie Grant Agreement No. 754510. This work was supported by Spanish MINECO (the Severo Ochoa Centers of Excellence Program under Grant No. SEV-2017-0706), Spanish MICIU, AEI and EU FEDER (Grant No. PGC2018-096955-B-C43), and Generalitat de Catalunya (Grant No. 2017SGR1506 and the CERCA Program). The work was also supported by the European Union MaX Center of Excellence (EU-H2020 Grant No. 824143).
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1053. Growth rate as a direct regulator of the start network to set cell size
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Martí Aldea, Kirsten Jenkins, Attila Csikász-Nagy, Ministerio de Economía y Competitividad (España), Ministerio de Ciencia e Innovación (España), and Engineering and Physical Sciences Research Council (UK)
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0301 basic medicine ,Mini Review ,Cells ,Cèl·lules ,Regulator ,Biology ,Cell cycle ,Cicle cel·lular ,Cell size ,03 medical and health sciences ,Cell and Developmental Biology ,Mathematical model ,Células ,Budding yeast ,Growth rate ,Set (psychology) ,lcsh:QH301-705.5 ,Crecimiento celular ,Cells-Growth ,Cell Biology ,Yeast ,Cell biology ,030104 developmental biology ,Size control ,lcsh:Biology (General) ,Function (biology) ,Developmental Biology - Abstract
Cells are able to adjust their growth and size to external inputs to comply with specific fates and developmental programs. Molecular pathways controlling growth also have an enormous impact in cell size, and bacteria, yeast, or epithelial cells modify their size as a function of growth rate. This universal feature suggests that growth (mass) and proliferation (cell number) rates are subject to general coordinating mechanisms. However, the underlying molecular connections are still a matter of debate. Here we review the current ideas on growth and cell size control, and focus on the possible mechanisms that could link the biosynthetic machinery to the Start network in budding yeast. In particular, we discuss the role of molecular chaperones in a competition framework to explain cell size control by growth at the individual cell level., Our work has been supported by grants from the Ministry of Economy and Competitiveness of Spain (BFU2016- 80234-R, BFU2013-47710, and Consolider-Ingenio 2010 CSD2007-15) and EPSRC Centre for Doctoral Training in Cross-Disciplinary Approaches to Non-Equilibrium Systems (CANES, EP/L015854/1)
1054. Immobilized graphene oxide-based membranes for improved pore wetting resistance in membrane distillation
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Monica Alberto, Clara Skuse, Marzieh Tamaddondar, Patricia Gorgojo, Engineering and Physical Sciences Research Council (UK), Agencia Estatal de Investigación (España), Ministerio de Ciencia, Innovación y Universidades (España), and Ministerio de Economía y Competitividad (España)
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Pore wetting resistance ,Mechanical Engineering ,General Chemical Engineering ,Surfactant ,General Materials Science ,Membrane distillation ,General Chemistry ,Wastewater treatment ,Water Science and Technology ,Graphene oxide - Abstract
Membrane distillation (MD) is a useful method for the purification of difficult feedwaters but it cannot be applied in a range of industries due to pore wetting. In this work, graphene oxide (GO) laminate coatings are explored to overcome the pore wetting issues. Air gap MD (AGMD) configuration was considered, using a 35 g L−1 NaCl solution with 150 mg L−1 (150 ppm) of Triton X-100 surfactant as feed material. The GO is deposited as a laminate membrane on top of a commercial porous polyvinylidene fluoride (PVDF) support and good adhesion is achieved through the use of polydopamine (PDA) to form a hydrophilic tri-layer membrane. The small pore size achieved with the laminate GO led to increased pore wetting resistance for at least 90 h compared to 20 min with pristine commercial PVDF. Additionally, the extra layers of GO and PDA did not affect the membrane flux. Overall, a tri-layer immobilized GO membrane is synthesized with superior performance when compared to current commercial membranes, meaning that MD can be used for a new range of wastewater applications., The authors acknowledge the Engineering and Physical Sciences Research Council (EPSRC) grant EP/S032258/1 for supporting this work. Clara Skuse would like to acknowledge the EPSRC for funding this work through the NOWNANO CDT. Patricia Gorgojo is grateful to the Spanish Ministerio de Economía y Competitividad and the European Social Fund for her Ramón y Cajal Fellowship (RYC2019-027060-I/AEI/10.13039/501100011033).
1055. Pathways to cellular supremacy in biocomputing
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Lewis Grozinger, Ruud Stoof, Diego A. Oyarzún, Martyn Amos, Huseyin Tas, Paolo Zuliani, Harold Fellermann, Angel Goñi-Moreno, Thomas E. Gorochowski, Pablo Carbonell, Engineering and Physical Sciences Research Council (UK), European Commission, and Royal Society (UK)
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0301 basic medicine ,Chemistry(all) ,Exploit ,Computer science ,Science ,Cells ,Distributed computing ,Computation ,General Physics and Astronomy ,BrisSynBio ,Physics and Astronomy(all) ,General Biochemistry, Genetics and Molecular Biology ,genetic circuits ,Computers, Molecular ,03 medical and health sciences ,Synthetic biology ,0302 clinical medicine ,Application areas ,Cellular computing ,lcsh:Science ,bioengineering ,Multidisciplinary ,Computers ,Biochemistry, Genetics and Molecular Biology(all) ,Model of computation ,Bristol BioDesign Institute ,C100 ,biocomputing ,General Chemistry ,Conceptual mapping ,Living systems ,030104 developmental biology ,Perspective ,cellular supremacy ,lcsh:Q ,DNA computing and cryptography ,030217 neurology & neurosurgery - Abstract
Synthetic biology uses living cells as the substrate for performing human-defined computations. Many current implementations of cellular computing are based on the “genetic circuit” metaphor, an approximation of the operation of silicon-based computers. Although this conceptual mapping has been relatively successful, we argue that it fundamentally limits the types of computation that may be engineered inside the cell, and fails to exploit the rich and diverse functionality available in natural living systems. We propose the notion of “cellular supremacy” to focus attention on domains in which biocomputing might offer superior performance over traditional computers. We consider potential pathways toward cellular supremacy, and suggest application areas in which it may be found., Synthetic biology uses cells as its computing substrate, often based on the genetic circuit concept. In this Perspective, the authors argue that existing synthetic biology approaches based on classical models of computation limit the potential of biocomputing, and propose that living organisms have under-exploited capabilities.
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1056. Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents
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Nuria Martinez-Saez, Gonzalo Jiménez-Osés, Maria João Matos, Elizabeth R. Perkins, Inês S. Albuquerque, Gonçalo J. L. Bernardes, Antonio C. B. Burtoloso, Pedro M. S. D. Cal, Francisco Corzana, Bruno L. Oliveira, Barbara Bernardim, Bernardim de Souza, Barbara [0000-0002-0554-2728], Lopes Bernardes, Goncalo [0000-0001-6594-8917], Apollo - University of Cambridge Repository, Fundação para a Ciência e a Tecnologia (Portugal), Fundação de Amparo à Pesquisa do Estado de São Paulo, Xunta de Galicia, European Commission, Royal Society (UK), Ministerio de Educación, Cultura y Deporte (España), Ministerio de Economía y Competitividad (España), European Research Council, and Engineering and Physical Sciences Research Council (UK)
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Protein Conformation, alpha-Helical ,Fluorophore ,Acetonitriles ,Immunoconjugates ,Receptor, ErbB-2 ,Science ,health care facilities, manpower, and services ,education ,General Physics and Astronomy ,Sulfides ,010402 general chemistry ,01 natural sciences ,Benzoates ,General Biochemistry, Genetics and Molecular Biology ,Article ,Maleimides ,chemistry.chemical_compound ,PEG ratio ,Humans ,Amino Acid Sequence ,Cysteine ,Annexin A5 ,health care economics and organizations ,chemistry.chemical_classification ,Multidisciplinary ,Bioconjugation ,Staining and Labeling ,010405 organic chemistry ,Chemistry ,Protein Stability ,Rational design ,Stereoisomerism ,General Chemistry ,Trastuzumab ,PROTEÍNAS ,Combinatorial chemistry ,0104 chemical sciences ,Cross-Linking Reagents ,HEK293 Cells ,Biochemistry ,Acrylates ,Reagent ,Thiol ,Protein Conformation, beta-Strand ,Conjugate - Abstract
This work is licensed under a Creative Commons Attribution 4.0 International License.-- et al., Maleimides remain the reagents of choice for the preparation of therapeutic and imaging protein conjugates despite the known instability of the resulting products that undergo thiol-exchange reactions in vivo. Here we present the rational design of carbonylacrylic reagents for chemoselective cysteine bioconjugation. These reagents undergo rapid thiol Michael-addition under biocompatible conditions in stoichiometric amounts. When using carbonylacrylic reagents equipped with PEG or fluorophore moieties, this method enables access to protein and antibody conjugates precisely modified at pre-determined sites. Importantly, the conjugates formed are resistant to degradation in plasma and are biologically functional, as demonstrated by the selective imaging and detection of apoptotic and HER2+ cells, respectively. The straightforward preparation, stoichiometric use and exquisite cysteine selectivity of the carbonylacrylic reagents combined with the stability of the products and the availability of biologically relevant cysteine-tagged proteins make this method suitable for the routine preparation of chemically defined conjugates for in vivo applications., We thank FAPESP (2012/22274-2; BEPE 2015/07509-1 to B.B., and 2013/25504-1 for A.C.B.B.), Xunta de Galicia (M.J.M.), FCT Portugal (FCT Investigator to G.J.L.B.; SFRH/BPD/103172/2014 Postdoctoral fellowship to P.M.S.D.C.; SFRH/BD/111556/2015 PhD Studentship to I.S.A.), the EU (Marie-Sklodowska Curie ITN Protein Conjugates), the EPSRC, MECD (‘Salvador Madariaga’ mobility grant PRX15/00638 to F.C.) and MINECO (CTQ2015-70524-R and RYC-2013-14706 to G.J.-O.) for funding. . G.J.L.B. is a Royal Society University Research Fellow and the recipient of an European Research Council Starting Grant (TagIt).
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1057. APC/C Cdh1 Enables Removal of Shugoshin-2 from the Arms of Bivalent Chromosomes by Moderating Cyclin-Dependent Kinase Activity
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Rattani, A, Ballesteros Mejia, R, Roberts, K, Roig, MB, Godwin, J, Hopkins, M, Eguren, M, Sanchez-Pulido, L, Okaz, E, Ogushi, S, Wolna, M, Metson, J, Pendás, AM, Malumbres, M, Novák, B, Herbert, M, Nasmyth, K, European Commission, Engineering and Physical Sciences Research Council (UK), Biotechnology and Biological Sciences Research Council (UK), Medical Research Council (UK), Wellcome Trust, Ministerio de Economía y Competitividad (España), and Boehringer Ingelheim Fonds
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Meiosis ,Shugoshin-2 ,Journal Article ,Aneuploidy ,Aurora kinase ,Cohesins ,health care economics and organizations - Abstract
In mammalian females, germ cells remain arrested as primordial follicles. Resumption of meiosis is heralded by germinal vesicle breakdown, condensation of chromosomes, and their eventual alignment on metaphase plates. At the first meiotic division, anaphase-promoting complex/cyclosome associated with Cdc20 (APC/C) activates separase and thereby destroys cohesion along chromosome arms. Because cohesion around centromeres is protected by shugoshin-2, sister chromatids remain attached through centromeric/pericentromeric cohesin. We show here that, by promoting proteolysis of cyclins and Cdc25B at the germinal vesicle (GV) stage, APC/C associated with the Cdh1 protein (APC/C) delays the increase in Cdk1 activity, leading to germinal vesicle breakdown (GVBD). More surprisingly, by moderating the rate at which Cdk1 is activated following GVBD, APC/C creates conditions necessary for the removal of shugoshin-2 from chromosome arms by the Aurora B/C kinase, an event crucial for the efficient resolution of chiasmata., A.R., R.B.M., and M. Hopkins were supported by PhD fellowships from the Boehringer Ingelheim Fonds, Barbour Foundation, and EPSRC (EP/G03706X/1), respectively. A.M.P. is supported by Ministerio de Economia y Competitividad (MINECO) (grant number: BFU-2014-59307); M. Herbert is funded by the Medical Research Council (MR/J003603/1), Wellcome Trust (096919), and European Community’s Horizon 2020 Research and Innovation Programme under grant agreement 634113 (GermAge); and B.N. is supported by a BBSRC Strategic LoLa grant (BB/M00354X/1). The European Community’s Seventh Framework MitoSys (241548), Medical Research Council (84673), and Wellcome Trust (019859/Z/10/Z) funded this project. Open Access funded by Wellcome Trust.
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1058. Probing 3D magnetic nanostructures by dark-field magneto-optical Kerr effect
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Dédalo Sanz-Hernández, Luka Skoric, Miguel Ángel Cascales-Sandoval, Amalio Fernández-Pacheco, University of Cambridge, Agence Nationale de la Recherche (France), Centre National de la Recherche Scientifique (France), European Commission, Gobierno de Aragón, and Engineering and Physical Sciences Research Council (UK)
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Magneto-optical Kerr effect ,Three dimensional ,General Physics and Astronomy ,Dark field ,Nanostructures - Abstract
Magneto-optical techniques are key tools for the characterization of magnetic effects at the nanoscale. Here, we present the dark-field magneto-optical Kerr effect (DFMOKE), a technique we have recently developed for the characterization of three-dimensional magnetic nanostructures. We introduce the principles of DFMOKE, based on the separation of an incident beam into multiple reflected beams when focusing on a 3D nano-geometry. We show the key modifications needed in a standard focused MOKE magnetometer to perform these measurements. Finally, we showcase the power of this method by detecting the magnetic switching of a single tilted 3D nanowire, independently from the switching of a magnetic thin film that surrounds it. We obtain independent and simultaneous switching detection of the nanowire and the film for all nanowire dimensions investigated, allowing us to estimate a magnetic sensitivity of 7 × 10-15 A m2 for DFMOKE in the setup used. We conclude the article by providing perspectives of future avenues where DFMOKE can be a very powerful characterization tool in future investigations of 3D magnetic nanostructures., DSH and AFP are grateful to the University of Cambridge, where part of this research was performed. DSH acknowledges funding from ANR/CNRS under the French Plan Relance de l’Etat for the preservation of R&D. This work was supported by the European Community under the Horizon 2020 Program, Contract No. 101001290 (3DNANOMAG), the MCIN with funding from European Union NextGenerationEU (PRTR-C17.I1), and the Aragon Government through the Project Q-MAD. L.S. acknowledges support from the EPSRC Cambridge NanoDTC EP/L015978/1
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