188 research outputs found

    Shubnikov-de Haas oscillations of a single layer graphene under dc current bias

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    Shubnikov-de Haas (SdH) oscillations under a dc current bias are experimentally studied on a Hall bar sample of single layer graphene. In dc resistance, the bias current shows the common damping effect on the SdH oscillations and the effect can be well accounted for by an elevated electron temperature that is found to be linearly dependent on the current bias. In differential resistance, a novel phase inversion of the SdH oscillations has been observed with increasing dc bias, namely we observe the oscillation maxima develop into minima and vice versa. Moreover, it is found that the onset biasing current, at which a SdH extremum is about to invert, is linearly dependent on the magnetic field of the SdH extrema. These observations are quantitatively explained with the help of a general SdH formula.Comment: 5 pages, 4 figures, A few references adde

    Who\u27s Carrying Capacity?

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    Two-grid methods of finite element approximation for parabolic integro-differential optimal control problems

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    In this paper, we present a two-grid scheme of fully discrete finite element approximation for optimal control problems governed by parabolic integro-differential equations. The state and co-state variables are approximated by a piecewise linear function and the control variable is discretized by a piecewise constant function. First, we derive the optimal a priori error estimates for all variables. Second, we prove the global superconvergence by using the recovery techniques. Third, we construct a two-grid algorithm and discuss its convergence. In the proposed two-grid scheme, the solution of the parabolic optimal control problem on a fine grid is reduced to the solution of the parabolic optimal control problem on a much coarser grid; additionally, the solution of a linear algebraic system on the fine grid and the resulting solution maintain an asymptotically optimal accuracy. Finally, we present a numerical example to verify the theoretical results

    Epitope mapping of PfCP-2.9, an asexual blood-stage vaccine candidate of Plasmodium falciparum

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    <p>Abstract</p> <p>Background</p> <p>Apical membrane antigen 1 (AMA-1) and merozoite surface protein 1 (MSP1) of <it>Plasmodium falciparum </it>are two leading blood-stage malaria vaccine candidates. A <it>P. falciparum </it>chimeric protein 2.9 (PfCP-2.9) has been constructed as a vaccine candidate, by fusing AMA-1 domain III (AMA-1 (III)) with a C-terminal 19 kDa fragment of MSP1 (MSP1-19) via a 28-mer peptide hinge. PfCP-2.9 was highly immunogenic in animal studies, and antibodies elicited by the PfCP-2.9 highly inhibited parasite growth <it>in vitro</it>. This study focused on locating the distribution of epitopes on PfCP-2.9.</p> <p>Methods</p> <p>A panel of anti-PfCP-2.9 monoclonal antibodies (mAbs) were produced and their properties were examined by Western blot as well as <it>in vitro </it>growth inhibition assay (GIA). In addition, a series of PfCP-2.9 mutants containing single amino acid substitution were produced in <it>Pichia pastoris</it>. Interaction of the mAbs with the PfCP-2.9 mutants was measured by both Western blot and enzyme-linked immunosorbent assay (ELISA).</p> <p>Results</p> <p>Twelve mAbs recognizing PfCP-2.9 chimeric protein were produced. Of them, eight mAbs recognized conformational epitopes and six mAbs showed various levels of inhibitory activities on parasite growth <it>in vitro</it>. In addition, seventeen PfCP-2.9 mutants with single amino acid substitution were produced in <it>Pichia pastoris </it>for interaction with mAbs. Reduced binding of an inhibitory mAb (mAb7G), was observed in three mutants including M62 (Phe<sup>491</sup>→Ala), M82 (Glu<sup>511</sup>→Gln) and M84 (Arg<sup>513</sup>→Lys), suggesting that these amino acid substitutions are critical to the epitope corresponding to mAb7G. The binding of two non-inhibitory mAbs (mAbG11.12 and mAbW9.10) was also reduced in the mutants of either M62 or M82. The substitution of Leu<sup>31 </sup>to Arg resulted in completely abolishing the binding of mAb1E1 (a blocking antibody) to M176 mutant, suggesting that the Leu residue at this position plays a crucial role in the formation of the epitope. In addition, the Asn<sup>15 </sup>residue may also play an important role in the global folding of PfCP-2.9, as its substitution by Arg lead to reduced binding of most mAbs and abolishing the binding of mAb6G and mAbP5-W12.</p> <p>Conclusions</p> <p>This study provided valuable information on epitopes of PfCP-2.9 vaccine candidate through generation of a panel of mAbs and a series of PfCP-2.9 mutants. The information may prove to be useful for designing more effective malaria vaccines against blood-stage parasites.</p

    Application of photo-crosslinkable gelatin methacryloyl in wound healing

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    Wound healing is a complex and coordinated biological process easily influenced by various internal and external factors. Hydrogels have immense practical importance in wound nursing because of their environmental moisturising, pain-relieving, and cooling effects. As photo-crosslinkable biomaterials, gelatine methacryloyl (GelMA) hydrogels exhibit substantial potential for tissue repair and reconstruction because of their tunable and beneficial properties. GelMA hydrogels have been extensively investigated as scaffolds for cell growth and drug release in various biomedical applications. They also hold great significance in wound healing because of their similarity to the components of the extracellular matrix of the skin and their favourable physicochemical properties. These hydrogels can promote wound healing and tissue remodelling by reducing inflammation, facilitating vascularisation, and supporting cell growth. In this study, we reviewed the applications of GelMA hydrogels in wound healing, including skin tissue engineering, wound dressing, and transdermal drug delivery. We aim to inspire further exploration of their potential for wound healing
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