1,034 research outputs found

    Coherence retrieval using trace regularization

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    The mutual intensity and its equivalent phase-space representations quantify an optical field's state of coherence and are important tools in the study of light propagation and dynamics, but they can only be estimated indirectly from measurements through a process called coherence retrieval, otherwise known as phase-space tomography. As practical considerations often rule out the availability of a complete set of measurements, coherence retrieval is usually a challenging high-dimensional ill-posed inverse problem. In this paper, we propose a trace-regularized optimization model for coherence retrieval and a provably-convergent adaptive accelerated proximal gradient algorithm for solving the resulting problem. Applying our model and algorithm to both simulated and experimental data, we demonstrate an improvement in reconstruction quality over previous models as well as an increase in convergence speed compared to existing first-order methods.Comment: 28 pages, 10 figures, accepted for publication in SIAM Journal on Imaging Science

    Simultaneous measurement and reconstruction tailoring for quantitative phase imaging

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    We propose simultaneous measurement and reconstruction tailoring (SMaRT) for quantitative phase imaging; it is a joint optimization approach to inverse problems wherein minimizing the expected end-to-end error yields optimal design parameters for both the measurement and reconstruction processes. Using simulated and experimentally-collected data for a specific scenario, we demonstrate that optimizing the design of the two processes together reduces phase reconstruction error over past techniques that consider these two design problems separately. Our results suggest at times surprising design principles, and our approach can potentially inspire improved solution methods for other inverse problems in optics as well as the natural sciences.Singapore-MIT Alliance. BioSystems and Micromechanics (BioSyM) Inter-Disciplinary Research GroupSingapore. National Research Foundatio

    Study on the Application of Hydrogen Fuel Cells in Passenge Cars and Prospects

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    The increasing demand for clean and sustainable energy sources has driven extensive research and development in the field of hydrogen fuel cell technology. This article provides an in-depth analysis of the advancements in hydrogen fuel cell technology and its potential application in passenger cars as a widely available, clean, and efficient energy source. By reviewing the current status of hydrogen fuel cells and national policies governing their implementation, this study aims to shed light on the development characteristics of China's hydrogen fuel cell industry, while also drawing comparisons with international hydrogen fuel cell policies and applications. Additionally, the article evaluates the performance of existing hydrogen fuel cell passenger cars in the market and proposes the application of future cutting-edge technologies to further enhance their capabilities. Through meticulous paraphrasing and enrichment, this scholarly work offers a comprehensive overview of hydrogen fuel cell technology, delves into the intricate landscape of the industry, and explores the promising prospects for its continued advancement. By encompassing a wide array of aspects related to hydrogen fuel cell technology, this article contributes to the academic discourse surrounding sustainable and efficient energy solutions for the transportation sector

    Functional identification of PGM1 in the regulating development and depositing of inosine monophosphate specific for myoblasts

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    BackgroundInosine monophosphate (IMP) is naturally present in poultry muscle and plays a key role in improving meat flavour. However, IMP deposition is regulated by numerous genes and complex molecular networks. In order to excavate key candidate genes that may regulate IMP synthesis, we performed proteome and metabolome analyses on the leg muscle, compared to the breast muscle control of 180-day-old Jingyuan chickens (hens), which had different IMP content. The key candidate genes identified by a differential analysis were verified to be associated with regulation of IMP-specific deposition.ResultsThe results showed that the differentially expressed (DE) proteins and metabolites jointly involve 14 metabolic pathways, among which the purine metabolic pathway closely related to IMP synthesis and metabolism is enriched with four DE proteins downregulated (with higher expression in breast muscles than in leg muscles), including adenylate kinase 1 (AK1), adenosine monophosphate deaminase 1 (AMPD1), pyruvate kinase muscle isoenzyme 2 (PKM2) and phosphoglucomutase 1 (PGM1), six DE metabolites, Hypoxanthine, Guanosine, L-Glutamine, AICAR, AMP and Adenylsuccinic acid. Analysis of PGM1 gene showed that the high expression of PGM1 promoted the proliferation and differentiation of myoblasts and inhibited the apoptosis of myoblasts. ELISA tests have shown that PGM1 reduced adenosine triphosphate (ATP) and IMP and uric acid (UA), while enhancing the biosynthesis of hypoxanthine (HX). In addition, up-regulation of PGM1 inhibited the expression of purine metabolism pathway related genes, and promoted the IMP de novo and salvage synthesis pathways.ConclusionThis study preliminarily explored the mechanism of action of PGM1 in regulating the growth and development of myoblasts and specific IMP deposition in Jingyuan chickens, which provided certain theoretical basis for the development and utilization of excellent traits in Jingyuan chickens

    Tuning electronic properties of epitaxial multilayer-graphene/4H–SiC(0001) by Joule heating decomposition in hydrogen

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    Abstract(#br)On the semi-insulating 4H–SiC (0001) surface, hydrogenated multilayers graphene (MLG) were epitaxially prepared by the method of Joule heating decomposition in the hydrogen atmosphere. The structural and chemical characteristics of multilayers graphene have been elaborately analyzed by the X-ray photoelectron and Raman spectroscopies, showing the level of hydrogenation being promoted with the increase of hydrogen pressure. Then, diodes with MLG/4H–SiC contact were fabricated and studied, proving that the Schottky barrier height (SBH) of MLG/4H–SiC junction was enhanced by the hydrogenation. By studying the typical current-voltage characteristics, the SBH was observed to be heightened from 0.84 eV to 1.0 eV along with the hydrogen pressure increasing from 10 −2 mbar to 10 2 mbar. Finally, graphene-semiconductor-graphene photodetectors were fabricated, showing peak responsivity as high as~ 0.9 A/W and external quantum efficiency of 345%, under the 324 nm illumination and biased at 3V

    Polypharmacology of Berberine Based on Multi-Target Binding Motifs

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    Background: Polypharmacology is emerging as the next paradigm in drug discovery. However, considerable challenges still exist for polypharmacology modeling. In this study, we developed a rational design to identify highly potential targets (HPTs) for polypharmacological drugs, such as berberine.Methods and Results: All the proven co-crystal structures locate berberine in the active cavities of a redundancy of aromatic, aliphatic, and acidic residues. The side chains from residues provide hydrophobic and electronic interactions to aid in neutralization for the positive charge of berberine. Accordingly, we generated multi-target binding motifs (MBM) for berberine, and established a new mathematical model to identify HPTs based on MBM. Remarkably, the berberine MBM was embodied in 13 HPTs, including beta-secretase 1 (BACE1) and amyloid-β1-42 (Aβ1-42). Further study indicated that berberine acted as a high-affinity BACE1 inhibitor and prevented Aβ1-42 aggregation to delay the pathological process of Alzheimer’s disease.Conclusion: Here, we proposed a MBM-based drug-target space model to analyze the underlying mechanism of multi-target drugs against polypharmacological profiles, and demonstrated the role of berberine in Alzheimer’s disease. This approach can be useful in derivation of rules, which will illuminate our understanding of drug action in diseases
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