1,650 research outputs found

    Achievable Performance in Product-Form Networks

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    We characterize the achievable range of performance measures in product-form networks where one or more system parameters can be freely set by a network operator. Given a product-form network and a set of configurable parameters, we identify which performance measures can be controlled and which target values can be attained. We also discuss an online optimization algorithm, which allows a network operator to set the system parameters so as to achieve target performance metrics. In some cases, the algorithm can be implemented in a distributed fashion, of which we give several examples. Finally, we give conditions that guarantee convergence of the algorithm, under the assumption that the target performance metrics are within the achievable range.Comment: 50th Annual Allerton Conference on Communication, Control and Computing - 201

    The protein challenge:Matching future demand and supply in Indonesia

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    Indonesia has the fourth largest population in the world and in the coming years food production will need to catch up with its growth. To fulfill the protein demand of this growing population, the productivity of the Indonesian agricultural sector should be increased. This can be achieved either by expanding the agricultural land or by increasing the productivity of existing agricultural land and protein use efficiency. An expansion of agricultural land is not always possible or desirable: large parts of Indonesia comprise forest areas, including tropical rain forests. Consequently, the optimization of the use of existing agricultural land is inevitable. The present manuscript describes and discusses the current protein consumption and production in Indonesia. It presents the levels predicted for 2035, which would imply a strong gap between consumption and production. Alternatives therefore need to be considered to avoid protein shortage in the future. These would include the use of new biomass resources, utilization of agricultural residues as alternative protein sources for feed and other nonfood applications, and biorefining of biomass sources.</p

    End-functional styrene-maleic anhydride copolymers via catalytic chain transfer polymerization

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    Styrene-maleic anhydride copolymers have been successfully synthesized using catalytic chain transfer polymerization employing the low spin [bis(difluoroboryl)dimethylglyoximato]cobalt(II) (COBF) complex. By partially replacing styrene with α-methylstyr

    The impact of entrepreneurship research on other academic fields

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    The remarkable ascent of entrepreneurship witnessed as a scientific field over the last 4 decades has been made possible by entrepreneurship’s ability to absorb theories, paradigms, and methods from other fields such as economics, psychology, sociology, geography, and even biology. The respectability of entrepreneurship as an academic discipline is now evidenced by many other fields starting to borrow from the entrepreneurship view. In the present paper, seven examples are given from this “pay back” development. These examples were first presented during a seminar at the Erasmus Entrepreneurship Event called what has the entrepreneurship view to offer to other academic fields? This article elaborates on the core ideas of these presentations and focuses on the overarching question of how entrepreneurship research impacts the development of other academic fields. We found that entrepreneurship research questions the core assumptions of other academic fields and provides new insights into the antecedents, mechanisms, and consequences of their respective core phenomena. Moreover, entrepreneurship research helps to legitimize other academic fields both practically and academically.</p

    Modelling the effects of ethanol on the solubility of the proteinogenic amino acids with the NRTL, Gude and Jouyban-Acree models

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    The addition of organic solvents, such as ethanol, to molecules in solution is an effective process for crystallization and is used in industrial settings (i.e. pharmaceutical production, downstream processing, etc.). In this study, we use solubility data of all proteinogenic α-amino acids in binary ethanol/water systems to model their excess solubility. We use the empirical and regressive models of Gude and NRTL and the predictive Jouyban-Acree model. Based on the results, we hypothesize that amino acids that are spherical and lack a reactive side chain show little or no excess solubility. Being rod-like and/or having a reactive side chain leads to a positive excess solubility in a mixed solvent of ethanol and water. The empirical and regressed models, NRTL and Gude, fit the data well and the predictive Jouyban-Acree model, not originally intended to be used for small molecules, is less accurate but offers insights into the thermodynamic properties of the amino acids

    Differential binding of neutralizing and non-neutralizing antibodies to native-like soluble HIV-1 Env trimers, uncleaved Env proteins, and monomeric subunits

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    Background: The trimeric envelope glycoproteins (Env) on the surface of HIV-1 virions are the targets for neutralizing antibodies (NAbs). No candidate HIV-1 immunogen has yet induced potent, broadly active NAbs (bNAbs). Part of the explanation may be that previously tested Env proteins inadequately mimic the functional, native Env complex. Trimerization and the proteolytic processing of Env precursors into gp120 and gp41 profoundly alter antigenicity, but soluble cleaved trimers are too unstable to serve as immunogens. By introducing stabilizing mutations (SOSIP), we constructed soluble, cleaved Env trimers derived from the HIV-1 subtype A isolate BG505 that resemble native Env spikes on virions both structurally and antigenically. Results: We used surface plasmon resonance (SPR) to quantify antibody binding to different forms of BG505 Env: the proteolytically cleaved SOSIP.664 trimers, cleaved gp120-gp41ECTO protomers, and gp120 monomers. Non-NAbs to the CD4-binding site bound only marginally to the trimers but equally well to gp120-gp41ECTO protomers and gp120 monomers, whereas the bNAb VRC01, directed to the CD4bs, bound to all three forms. In contrast, bNAbs to V1V2 glycan-dependent epitopes bound preferentially (PG9 and PG16) or exclusively (PGT145) to trimers. We also explored the antigenic consequences of three different features of SOSIP.664 gp140 trimers: the engineered inter-subunit disulfide bond, the trimer-stabilizing I559P change in gp41ECTO, and proteolytic cleavage at the gp120-gp41ECTO junction. Each of these three features incrementally promoted native-like trimer antigenicity. We compared Fab and IgG versions of bNAbs and validated a bivalent model of IgG binding. The NAbs showed widely divergent binding kinetics and degrees of binding to native-like BG505 SOSIP.664. High off-rate constants and low stoichiometric estimates of NAb binding were associated with large amounts of residual infectivity after NAb neutralization of the corresponding BG505.T332N pseudovirus. Conclusions: The antigenicity and structural integrity of cleaved BG505 SOSIP.664 trimers render these proteins good mimics of functional Env spikes on virions. In contrast, uncleaved gp140s antigenically resemble individual gp120-gp41ECTO protomers and gp120 monomers, but not native trimers. Although NAb binding to functional trimers may thus be both necessary and sufficient for neutralization, the kinetics and stoichiometry of the interaction influence the neutralizing efficacy of individual NAbs
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