87 research outputs found

    3D Printed Bioplastics with Shape-Memory Behavior Based on Native Bovine Serum Albumin

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    Unformatted postprintBio-based plastics that can supplant petroleum-derived materials are necessary to meet the future demands of sustainability in the life cycle of plastic materials. While there are significant efforts to develop protein-based plastic materials for commercial use, their application is limited by poor processability and limitations in mechanical performance. Here, we present a bovine serum albumin (BSA)-based resin for stereolithographic apparatus (SLA) 3D printing that affords bioplastic objects with shape memory behavior. We demonstrate that the native conformation of these globular proteins is largely retained in the 3D printed constructs, and that each protein molecule possesses a “stored length” that could be revealed during mechanical deformation (extension or compression) of the 3D bioplastic objects. While the plastically deformed objects could retain this state for an indefinite period of time, heating the object or submerging in water allowed it to return to its original 3D printed shape.We thank the Center for Research in Education and Simulation Technologies (CREST) at The University of Washington, and in particular Alex Gong for his assistance during the tensile tests. E.S.-R. thanks the European funding by the Marie Sklodowska-Curie Individual Fellowships (MSCA-IF-GF) 841879-4D Biogel. H.S. and A.G.-L. thank MINECO for funding through MAT2017-83373-R. A.N. thanks the National Science Foundation for support (1752972). A.L.C. thanks the European Research Council ERC-CoG-648071-ProNANO, and Agencia Estatal de Investigación, Spain (PID2019-111649RB-I00). This work was performed partially under the Maria de Maeztu Units of Excellence Program from the Spanish State Research Agency – Grant No. MDM-2017-0720 (CIC biomaGUNE)

    Meiotic Regulation of TPX2 Protein Levels Governs Cell Cycle Progression in Mouse Oocytes

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    Formation of female gametes requires acentriolar spindle assembly during meiosis. Mitotic spindles organize from centrosomes and via local activation of the RanGTPase on chromosomes. Vertebrate oocytes present a RanGTP gradient centred on chromatin at all stages of meiotic maturation. However, this gradient is dispensable for assembly of the first meiotic spindle. To understand this meiosis I peculiarity, we studied TPX2, a Ran target, in mouse oocytes. Strikingly, TPX2 activity is controlled at the protein level through its accumulation from meiosis I to II. By RNAi depletion and live imaging, we show that TPX2 is required for spindle assembly via two distinct functions. It controls microtubule assembly and spindle pole integrity via the phosphorylation of TACC3, a regulator of MTOCs activity. We show that meiotic spindle formation in vivo depends on the regulation of at least a target of Ran, TPX2, rather than on the regulation of the RanGTP gradient itself

    The nucleoporin ALADIN regulates Aurora A localization to ensure robust mitotic spindle formation

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    The formation of the mitotic spindle is a complex process that requires massive cellular reorganization. Regulation by mitotic kinases controls this entire process. One of these mitotic controllers is Aurora A kinase, which is itself highly regulated. In this study, we show that the nuclear pore protein ALADIN is a novel spatial regulator of Aurora A. Without ALADIN, Aurora A spreads from centrosomes onto spindle microtubules, which affects the distribution of a subset of microtubule regulators and slows spindle assembly and chromosome alignment. ALADIN interacts with inactive Aurora A and is recruited to the spindle pole after Aurora A inhibition. Of interest, mutations in ALADIN cause triple A syndrome. We find that some of the mitotic phenotypes that we observe after ALADIN depletion also occur in cells from triple A syndrome patients, which raises the possibility that mitotic errors may underlie part of the etiology of this syndrome

    Ionospheric modelling using GPS to calibrate the MWA. 1 : Comparison of first order ionospheric effects between GPS models and MWA observations

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    This document is the Accepted Manuscript version of the following article: B. S. Arora, et al, ‘Ionospheric Modelling using GPS to Calibrate the MWA. I: Comparison of First Order Ionospheric Effects between GPS Models and MWA Observations’, Publications of the Astronomical Society of Australia, Vol. 32, e029, August 2015. The final, published version is available online at doi: https://doi.org/10.1017/pasa.2015.29. COPYRIGHT: © Astronomical Society of Australia 2015.We compare first order (refractive) ionospheric effects seen by the Murchison Widefield Array (MWA) with the ionosphere as inferred from Global Positioning System (GPS) data. The first order ionosphere manifests itself as a bulk position shift of the observed sources across an MWA field of view. These effects can be computed from global ionosphere maps provided by GPS analysis centres, namely the Center for Orbit Determination in Europe (CODE), using data from globally distributed GPS receivers. However, for the more accurate local ionosphere estimates required for precision radio astronomy applications, data from local GPS networks needs to be incorporated into ionospheric modelling. For GPS observations, the ionospheric parameters are biased by GPS receiver instrument delays, among other effects, also known as receiver Differential Code Biases (DCBs). The receiver DCBs need to be estimated for any non-CODE GPS station used for ionosphere modelling, a requirement for establishing dense GPS networks in arbitrary locations in the vicinity of the MWA. In this work, single GPS station-based ionospheric modelling is performed at a time resolution of 10 minutes. Also the receiver DCBs are estimated for selected Geoscience Australia (GA) GPS receivers, located at Murchison Radio Observatory (MRO1), Yarragadee (YAR3), Mount Magnet (MTMA) and Wiluna (WILU). The ionospheric gradients estimated from GPS are compared with the ionospheric gradients inferred from radio source position shifts observed with the MWA. The ionospheric gradients at all the GPS stations show a correlation with the gradients observed with the MWA. The ionosphere estimates obtained using GPS measurements show promise in terms of providing calibration information for the MWA.Peer reviewe

    Use of anticoagulants and antiplatelet agents in stable outpatients with coronary artery disease and atrial fibrillation. International CLARIFY registry

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    Cholinium-based ion gels as solid electrolytes for long-term cutaneous electrophysiology

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    Cholinium-based bio-ion gels were prepared by photopolymerization of poly(cholinium lactate methacrylate) network within cholinium lactate ionic liquid. The rheological and thermal properties as well as ionic conductivity of ion gels of different compositions were measured. As indicated by rheological measurements, the ion gels show the properties of gel materials which become soft by increasing the amount of free ionic liquid. Cholinium ion gels with various composition of free ionic liquid vs. methacrylic network show glass transitions between -40° and -70 °C and thermal stability up to 200 °C. The ionic conductivity of these gels increases from 10-8 to 10-3 S cm-1 at 20 °C by varying the amount of free ionic liquid between 0 and 60 wt%, respectively. Low glass transition temperature and enhanced ionic conductivity make the cholinium-based ion gels good candidates to be used as a solid electrolytic interface between the skin and an electrode. The ion gels decrease the impedance with the human skin to levels that are similar to commercial Ag/AgCl electrodes. Accurate physiologic signals such as electrocardiography (ECG) were recorded with ion gels assisted electrodes for a long period of time (up to 72 h) with a remarkable stability. The low toxicity and superior ambient stability of cholinium ionic liquids and ion gels make these materials highly attractive for long-term cutaneous electrophysiology and other biomedical applications

    Stereocomplexed Functional and Statistical Poly(lactide-carbonate)s via a Simple Organocatalytic System

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    The stereocomplexation of polylactide (PLA) has been widely relied upon to develop degradable, sustainable materials with increased strength and improved material properties in comparison to stereopure PLA. However, forming functionalized copolymers of PLA while retaining high crystallinity remains elusive. Herein, the controlled ring-opening copolymerization (ROCOP) of lactide (LA) and functionalized cyclic carbonate monomers is undertaken. The produced polymers are shown to remain crystalline up to 25 mol % carbonate content and are efficiently stereocomplexed with homopolymer PLA and copolymers of opposite chirality. Polymers with alkene and alkyne pendent handles are shown to undergo efficient derivatization with thiol–ene click chemistry, which would allow both the covalent conjugation of therapeutic moieties and tuning of material properties
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