4,633 research outputs found

    SUMO-2 promotes mRNA translation by enhancing interaction between eIF4E and eIF4G

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    Small ubiquitin-like modifier (SUMO) proteins regulate many important eukaryotic cellular processes through reversible covalent conjugation to target proteins. In addition to its many well-known biological consequences, like subcellular translocation of protein, subnuclear structure formation, and modulation of transcriptional activity, we show here that SUMO-2 also plays a role in mRNA translation. SUMO-2 promoted formation of the active eukaryotic initiation factor 4F (eIF4F) complex by enhancing interaction between Eukaryotic Initiation Factor 4E (eIF4E) and Eukaryotic Initiation Factor 4G (eIF4G), and induced translation of a subset of proteins, such as cyclinD1 and c-myc, which essential for cell proliferation and apoptosis. As expected, overexpression of SUMO-2 can partially cancel out the disrupting effect of 4EGI-1, a small molecule inhibitor of eIF4E/eIF4G interaction, on formation of the eIF4F complex, translation of the cap-dependent protein, cell proliferation and apoptosis. On the other hand, SUMO-2 knockdown via shRNA partially impaired cap-dependent translation and cell proliferation and promoted apoptosis. These results collectively suggest that SUMO-2 conjugation plays a crucial regulatory role in protein synthesis. Thus, this report might contribute to the basic understanding of mammalian protein translation and sheds some new light on the role of SUMO in this process. © 2014 Chen et al

    An iterative substructuring approach to the calculation of eigensolution and eigensensitivity

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    Author name used in this manuscript: You-Lin Xu2010-2011 > Academic research: refereed > Publication in refereed journalAccepted ManuscriptPublishe

    Substructure based approach to finite element model updating

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    Author name used in this manuscript: You-Lin Xu2010-2011 > Academic research: refereed > Publication in refereed journalAccepted ManuscriptPublishe

    Noise auto-correlation spectroscopy with coherent Raman scattering

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    Ultrafast lasers have become one of the most powerful tools in coherent nonlinear optical spectroscopy. Short pulses enable direct observation of fast molecular dynamics, whereas broad spectral bandwidth offers ways of controlling nonlinear optical processes by means of quantum interferences. Special care is usually taken to preserve the coherence of laser pulses as it determines the accuracy of a spectroscopic measurement. Here we present a new approach to coherent Raman spectroscopy based on deliberately introduced noise, which increases the spectral resolution, robustness and efficiency. We probe laser induced molecular vibrations using a broadband laser pulse with intentionally randomized amplitude and phase. The vibrational resonances result in and are identified through the appearance of intensity correlations in the noisy spectrum of coherently scattered photons. Spectral resolution is neither limited by the pulse bandwidth, nor sensitive to the quality of the temporal and spectral profile of the pulses. This is particularly attractive for the applications in microscopy, biological imaging and remote sensing, where dispersion and scattering properties of the medium often undermine the applicability of ultrafast lasers. The proposed method combines the efficiency and resolution of a coherent process with the robustness of incoherent light. As we demonstrate here, it can be implemented by simply destroying the coherence of a laser pulse, and without any elaborate temporal scanning or spectral shaping commonly required by the frequency-resolved spectroscopic methods with ultrashort pulses.Comment: To appear in Nature Physic

    Enumeration of distinct mechanically stable disk packings in small systems

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    We create mechanically stable (MS) packings of bidisperse disks using an algorithm in which we successively grow or shrink soft repulsive disks followed by energy minimization until the overlaps are vanishingly small. We focus on small systems because this enables us to enumerate nearly all distinct MS packings. We measure the probability to obtain a MS packing at packing fraction ϕ\phi and find several notable results. First, the probability is highly nonuniform. When averaged over narrow packing fraction intervals, the most probable MS packing occurs at the highest ϕ\phi and the probability decays exponentially with decreasing ϕ\phi. Even more striking, within each packing-fraction interval, the probability can vary by many orders of magnitude. By using two different packing-generation protocols, we show that these results are robust and the packing frequencies do not change qualitatively with different protocols.Comment: 4 pages, 3 figures, Conference Proceedings for X International Workshop on Disordered System

    Improved substructuring method for eigensolutions of large-scale structures

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    Author name used in this manuscript: You-Lin Xu2008-2009 > Academic research: refereed > Publication in refereed journalAccepted ManuscriptPublishe

    Inverse substructure method for model updating of structures

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    2011-2012 > Academic research: refereed > Publication in refereed journalAccepted ManuscriptPublishe

    Variation of structural vibration characteristics versus non-uniform temperature distribution

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    Author name used in this manuscript: You-Lin Xu2010-2011 > Academic research: refereed > Publication in refereed journalAccepted ManuscriptPublishe

    Cellulose acetate in wound dressings formulations: potentialities and electrospinning capability

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    Série: IFMBE Proceedings, vol. 76Any open wound is a potential site for microorganisms’ invasion since their presence around us is inevitable. Skin wound healing relies on a series of complex physiochemical processes that remain a big challenge for healthcare professionals, particularly when the wounds are colonized by bacteria. Wound dressings play a major role in wound healing as they manage the wounded site, controlling the moisture balance and protecting the wound from repeated trauma, and by preventing possible infections from developing into more serious complications. Recently, bioactive dressings loaded with drugs and/or antimicrobial agents, allowing for a continuous and sustainable release of these molecules at the wounded site, have appeared in the market. Antimicrobial resistance is a growing health care problem, requiring more effective solutions than antibiotics. As such, nano- and microfibrous mats produced via electrospinning technique and loaded with natural-origin antimicrobial agents have attracted a lot of attention. Various polymers have been applied to engineer nanofibrous electrospun dressings. However, the environment impact of the synthesis and processing methods of synthetic polymers is undesirable. Therefore, the application of cellulose-derived materials (highly abundant polymer of natural-origin) becomes crucial as a green alternative to produce electrospun wound dressings with superior wettability, breathability and high capacity to promote cell proliferation, at relatively low costs. In this paper, different biomolecules loaded onto cellulose acetate (CA)-based polymeric nanofibers were investigated, and their antimicrobial properties were highlighted as alternatives to conventional antibiotics.Authors acknowledge the Portuguese Foundation for Science and Technology (FCT), FEDER funds by means of Competitive Factors Operational Program (POCI) for funding the projects POCI-01-0145-FEDER-028074 and UID/CTM/00264/2019
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