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461.
In a stochastic environment pooling naturally leads to economies of scale, but heterogeneity can also create variability. In the article, we investigate this trade-off in the case of a manufacturing environment. Pooling for queueing systems has been widely investigated in the literature on the design of service systems; however, much less attention has been given to manufacturing systems where jobs are given a due date upon arrival. In such systems it is not the elapsed time until the actual completion of the job that counts, but rather the due date lead time that can be promised to the customer in order to guarantee a high service level. The purpose of the article is to get a deeper understanding about how pooling strategies and lead-time decisions can be implemented to attain a high due-date performance. To this end, we develop a simulation and analytical study to determine the benefits of pooling manufacturing systems with heterogeneous demand streams. Our work allows managers to identify the characteristics of production systems such that a pooling strategy would be beneficial. Our results demonstrate that when a due-date setting and scheduling mechanism is implemented, heterogeneity does generally not lead to deterioration of performance, as previously observed in service environments. Our studies also reveal that the benefits of pooling in terms of the expected sojourn time obtained by a simple analytical treatment can serve as a good prediction of the benefits of pooling on the average due date lead time in a wide range of situations. 相似文献
462.
463.
Frontispiece: Bottom‐Up Fabrication of Nanopatterned Polymers on DNA Origami by In Situ Atom‐Transfer Radical Polymerization
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464.
Bottom‐Up Fabrication of Nanopatterned Polymers on DNA Origami by In Situ Atom‐Transfer Radical Polymerization
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Yu Tokura Yanyan Jiang Dr. Alexander Welle Prof. Martina H. Stenzel Katarzyna M. Krzemien Prof. Jens Michaelis Dr. Rüdiger Berger Prof. Christopher Barner‐Kowollik Dr. Yuzhou Wu Prof. Tanja Weil 《Angewandte Chemie (International ed. in English)》2016,55(19):5692-5697
Bottom‐up strategies to fabricate patterned polymers at the nanoscale represent an emerging field in the development of advanced nanodevices, such as biosensors, nanofluidics, and nanophotonics. DNA origami techniques provide access to distinct architectures of various sizes and shapes and present manifold opportunities for functionalization at the nanoscale with the highest precision. Herein, we conduct in situ atom‐transfer radical polymerization (ATRP) on DNA origami, yielding differently nanopatterned polymers of various heights. After cross‐linking, the grafted polymeric nanostructures can even stably exist in solution without the DNA origami template. This straightforward approach allows for the fabrication of patterned polymers with low nanometer resolution, which provides access to unique DNA‐based functional hybrid materials. 相似文献
465.
Laura von Lüders Rita Tilmann Dr. Kangho Lee Dr. Cian Bartlam Dr. Tanja Stimpel-Lindner Dr. Tarja K. Nevanen Dr. Kristiina Iljin Dr. Kathrin C. Knirsch Prof. Dr. Andreas Hirsch Prof. Dr. Georg S. Duesberg 《Angewandte Chemie (International ed. in English)》2023,62(22):e202219024
We report on a controllable and specific functionalisation route for graphene field-effect transistors (GFETs) for the recognition of small physiologically active molecules. Key element is the noncovalent functionalisation of the graphene surface with perylene bisimide (PBI) molecules directly on the growth substrate. This Functional Layer Transfer enables the homogeneous self-assembly of PBI molecules on graphene, onto which antibodies are subsequently immobilised. The sensor surface was characterised by atomic force microscopy, Raman spectroscopy and electrical measurements, showing superior performance over conventional functionalisation after transfer. Specific sensing of small molecules was realised by monitoring the electrical property changes of functionalised GFET devices upon the application of methamphetamine and cortisol. The concentration dependent electrical response of our sensors was determined down to a concentration of 300 ng ml−1 for methamphetamine. 相似文献
466.
The lubrication properties of adsorbed poly(L-lysine)-graft-poly(ethylene glycol) in aqueous buffer solution were studied with the surface forces apparatus. In general, the polymer brushes revealed extremely low friction forces. Two distinct regimes could be identified. In response to lateral shear, the friction forces of intact polymer films at moderate loads were below the detection limit. At high loads, when the films were compressed to about 10% of the original equilibrium film thickness, the friction showed a reversible increase with load. Under certain conditions, film destruction was observed, immediately followed by a dramatic increase in the frictional force and an expansion of the adsorbed brush layer. By the addition of free polymer to the buffer solution, the resistance of the polymer brushes to abrasion was dramatically increased by readsorption of the polymer following friction-induced desorption. This self-healing capacity and the extremely low friction of the adsorbed copolymer films contribute to their excellent properties as lubricant additives for water-based lubrication under boundary conditions. 相似文献
467.
In this paper we define partially ordered quasi-uniform spaces (X,
, ≤) (PO-quasi-uniform spaces) as those space with a biconvex quasi-uniformity
on the poset (X, ≤) and give a construction of a (transitive) biconvex compatible quasi-uniformity on a partially ordered topological space
when its topology satisfies certain natural conditions. We also show that under certain conditions on the topology
of a PO-quasi-uniform space (X,
, ≤), the bicompletion
of (X,
) is also a PO-quasi-uniform space (
, ⪯) with a partial order ⪯ on
that extends ≤ in a natural way.
相似文献
468.
Voss CV Gruber CC Faber K Knaus T Macheroux P Kroutil W 《Journal of the American Chemical Society》2008,130(42):13969-13972
Black and white are opposites as are oxidation and reduction. Performing an oxidation, for example, of a sec-alcohol and a reduction of the corresponding ketone in the same vessel without separation of the reagents seems to be an impossible task. Here we show that oxidative cofactor recycling of NADP (+) and reductive regeneration of NADH can be performed simultaneously in the same compartment without significant interference. Regeneration cycles can be run in opposing directions beside each other enabling one-pot transformation of racemic alcohols to one enantiomer via concurrent enantioselective oxidation and asymmetric reduction employing defined alcohol dehydrogenases with opposite stereo- and cofactor-preference. Thus, by careful selection of appropriate enzymes, NADH recycling can be performed in the presence of NADP (+) recycling to achieve overall, for example, deracemisation of sec-alcohols or stereoinversion representing a possible concept for a "green" equivalent to the chemical-intensive Mitsunobu inversion. 相似文献
469.
Mladenovic M Fink RF Thiel W Schirmeister T Engels B 《Journal of the American Chemical Society》2008,130(27):8696-8705
Papain-like cysteine proteases are ubiquitous proteolytic enzymes. The protonated His199/deprotonated Cys29 ion pair (cathepsin B numbering) in the active site is essential for their proper functioning. The presence of this ion pair stands in contrast to the corresponding intrinsic residue p K a values, indicating a strong influence of the enzyme environment. In the present work we show by molecular dynamics simulations on quantum mechanical/molecular mechanical (QM/MM) potentials that the ion pair is stabilized by a complex hydrogen bond network which comprises several amino acids situated in the active site of the enzyme and 2-4 water molecules. QM/MM reaction path computations for the proton transfer from His199 to the thiolate of the Cys29 moiety indicate that the ion pair is about 32-36 kJ mol (-1) more stable than the neutral form if the whole hydrogen bonding network is active. Without any hydrogen bonding network the ion pair is predicted to be significantly less stable than the neutral form. QM/MM charge deletion analysis and QM model calculations are used to quantify the stabilizing effect of the active-site residues and the L1 helix in favor of the zwitterionic form. The active-site water molecules contribute about 30 kJ mol (-1) to the overall stabilization. Disruption of the hydrogen bonding network upon substrate binding is expected to enhance the nucleophilic reactivity of the thiolate. 相似文献
470.
Kirschbaum M Jaeger MS Schenkel T Breinig T Meyerhans A Duschl C 《Journal of chromatography. A》2008,1202(1):83-89
The gentle and careful in vitro processing of live cells is essential in order to make them available to future therapeutic applications. We present a protocol for the activation of single-T cells based on the contact formation with individual anti-CD3/anti-CD28 presenting microbeads in a lab-on-chip environment. The chips consist of microfluidic channels and microelectrodes for performing dielectrophoretic manipulation employing a.c. electric fields. The dielectrophoretic guiding elements allow the assembly of cell-bead pairs while avoiding ill-defined physical contacts with their environment. After overnight cultivation of the manipulated cells, 77% of the bead-associated T cells expressed the activation marker molecule CD69. Physiological stress on the cells was shown to be mainly due to the single-cell cultivation and not to the manipulation in the chips. The same approach could be useful for the in vitro regulation of stem cell differentiation. 相似文献