101 research outputs found

    Atomic resolution structure of serine protease proteinase K at ambient temperature

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    Atomic resolution structures (beyond 1.20 ?) at ambient temperature, which is usually hampered by the radiation damage in synchrotron X-ray crystallography (SRX), will add to our understanding of the structure-function relationships of enzymes. Serial femtosecond crystallography (SFX) has attracted surging interest by providing a route to bypass such challenges. Yet the progress on atomic resolution analysis with SFX has been rather slow. In this report, we describe the 1.20 ? resolution structure of proteinase K using 13 keV photon energy. Hydrogen atoms, water molecules, and a number of alternative side-chain conformations have been resolved. The increase in the value of B-factor in SFX suggests that the residues and water molecules adjacent to active sites were flexible and exhibited dynamic motions at specific substrate-recognition sites. ? 2017 The Author(s).114Ysciescopu

    Hydroxyethyl cellulose matrix applied to serial crystallography

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    Serial femtosecond crystallography (SFX) allows structures of proteins to be determined at room temperature with minimal radiation damage. A highly viscous matrix acts as a crystal carrier for serial sample loading at a low flow rate that enables the determination of the structure, while requiring consumption of less than 1 mg of the sample. However, a reliable and versatile carrier matrix for a wide variety of protein samples is still elusive. Here we introduce a hydroxyethyl cellulose-matrix carrier, to determine the structure of three proteins. The de novo structure determination of proteinase K from single-wavelength anomalous diffraction (SAD) by utilizing the anomalous signal of the praseodymium atom was demonstrated using 3,000 diffraction images. ? 2017 The Author(s).113Ysciescopu

    Soft X-ray harmonic comb from relativistic electron spikes

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    We demonstrate a new high-order harmonic generation mechanism reaching the `water window' spectral region in experiments with multi-terawatt femtosecond lasers irradiating gas jets. A few hundred harmonic orders are resolved, giving uJ/sr pulses. Harmonics are collectively emitted by an oscillating electron spike formed at the joint of the boundaries of a cavity and bow wave created by a relativistically self-focusing laser in underdense plasma. The spike sharpness and stability are explained by catastrophe theory. The mechanism is corroborated by particle-in-cell simulations

    X-ray harmonic comb from relativistic electron spikes

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    X-ray devices are far superior to optical ones for providing nanometre spatial and attosecond temporal resolutions. Such resolution is indispensable in biology, medicine, physics, material sciences, and their applications. A bright ultrafast coherent X-ray source is highly desirable, for example, for the diffractive imaging of individual large molecules, viruses, or cells. Here we demonstrate experimentally a new compact X-ray source involving high-order harmonics produced by a relativistic-irradiance femtosecond laser in a gas target. In our first implementation using a 9 Terawatt laser, coherent soft X-rays are emitted with a comb-like spectrum reaching the 'water window' range. The generation mechanism is robust being based on phenomena inherent in relativistic laser plasmas: self-focusing, nonlinear wave generation accompanied by electron density singularities, and collective radiation by a compact electric charge. The formation of singularities (electron density spikes) is described by the elegant mathematical catastrophe theory, which explains sudden changes in various complex systems, from physics to social sciences. The new X-ray source has advantageous scalings, as the maximum harmonic order is proportional to the cube of the laser amplitude enhanced by relativistic self-focusing in plasma. This allows straightforward extension of the coherent X-ray generation to the keV and tens of keV spectral regions. The implemented X-ray source is remarkably easily accessible: the requirements for the laser can be met in a university-scale laboratory, the gas jet is a replenishable debris-free target, and the harmonics emanate directly from the gas jet without additional devices. Our results open the way to a compact coherent ultrashort brilliant X-ray source with single shot and high-repetition rate capabilities, suitable for numerous applications and diagnostics in many research fields

    Antisense epidermal growth factor receptor RNA transfection in human glioblastoma cells down-regulates telomerase activity and telomere length

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    Epidermal growth factor receptor is overexpressed and/or amplified in up to 50% of glioblastomas, suggesting an important role of this gene in glial tumorigenesis and progression. In the present study we demonstrated that epidermal growth factor receptor is involved in regulation of telomerase activity in glioblastoma. Antisense-epidermal growth factor receptor approach was used to inhibit epidermal growth factor receptor expression of glioblastoma U87MG cells. Telomerase activity in antisense-epidermal growth factor receptor cells decreased by up to 54 folds compared with control cells. Moreover, the telomere lengths of antisense-epidermal growth factor receptor cells were shortened. In addition, the tumorigenicity of antisense-epidermal growth factor receptor cells was significantly inhibited. Taken together, there were strong correlations between tumorigenicity and epidermal growth factor receptor expression levels, and between tumorigenicity and telomerase activity. These results provide evidence that epidermal growth factor receptor plays an important role in the regulation of telomerase activity of glioma cells. Our findings provide new insights into both the biological functions of epidermal growth factor receptor and the regulation of telomerase activity. The inhibition of telomerase activity triggered by antisense-epidermal growth factor receptor treatment may reflect yet another mechanism of antisense-epidermal growth factor receptor approach in tumour suppression

    Oil-free hyaluronic acid matrix for serial femtosecond crystallography

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    The grease matrix was originally introduced as a microcrystal-carrier for serial femtosecond crystallography and has been expanded to applications for various types of proteins, including membrane proteins. However, the grease-based matrix has limited application for oil-sensitive proteins. Here we introduce a grease-free, water-based hyaluronic acid matrix. Applications for proteinase K and lysozyme proteins were able to produce electron density maps at 2.3-angstrom resolution.open111011sciescopu

    MolecularĀ mechanismsĀ ofĀ vaspinĀ action: fromĀ adiposeĀ tissueĀ toĀ skinĀ andĀ bone,Ā fromĀ bloodĀ  vesselsĀ toĀ theĀ brainĀ 

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    VisceralĀ adiposeĀ tissue derivedĀ serineĀ proteaseĀ inhibitorĀ (vaspin)Ā orĀ SERPINA12Ā accordingĀ toĀ theĀ serpinĀ nomenclatureĀ wasĀ identifiedĀ togetherĀ withĀ otherĀ genesĀ andĀ geneĀ productsĀ thatĀ  wereĀ specificallyĀ expressedĀ orĀ overexpressedĀ inĀ theĀ intra abdominalĀ orĀ visceralĀ adiposeĀ tissueĀ  (AT)Ā ofĀ theĀ OtsukaĀ Long-EvansĀ TokushimaĀ fattyĀ rat.Ā TheseĀ ratsĀ spontaneouslyĀ developĀ visceralĀ  obesity,Ā insulinĀ resistance,Ā hyperinsulinemiaĀ andĀ ā€glycemia,Ā asĀ wellĀ asĀ hypertensionĀ andĀ thusĀ representĀ aĀ wellĀ suitedĀ animalĀ modelĀ ofĀ obesityĀ andĀ relatedĀ metabolicĀ disordersĀ suchĀ asĀ typeĀ  2Ā diabetes.Ā  TheĀ follow-upĀ studyĀ reportingĀ theĀ cloning,Ā expressionĀ andĀ functionalĀ characterizationĀ ofĀ  vaspinĀ suggestedĀ theĀ greatĀ andĀ promisingĀ potentialĀ ofĀ thisĀ moleculeĀ toĀ counteractĀ obesityĀ inducedĀ insulinĀ resistanceĀ andĀ inflammationĀ andĀ hasĀ sinceĀ initiatedĀ overĀ 300Ā publications,Ā clinicalĀ andĀ experimental,Ā thatĀ haveĀ contributedĀ toĀ uncoverĀ theĀ multifacetedĀ functionsĀ andĀ molecularĀ mechanismsĀ ofĀ vaspinĀ actionĀ notĀ onlyĀ inĀ theĀ adipose,Ā butĀ inĀ manyĀ differentĀ cells,Ā tissuesĀ andĀ organs.Ā ThisĀ reviewĀ willĀ giveĀ anĀ updateĀ onĀ mechanisticĀ andĀ structuralĀ aspectsĀ ofĀ vaspinĀ withĀ aĀ focusĀ onĀ itsĀ serpinĀ function,Ā theĀ physiologyĀ andĀ regulationĀ ofĀ vaspinĀ expression,Ā andĀ willĀ summarizeĀ theĀ latestĀ onĀ vaspinĀ functionĀ inĀ variousĀ tissuesĀ suchĀ asĀ theĀ differentĀ adiposeĀ tissueĀ depotsĀ asĀ wellĀ asĀ theĀ vasculature,Ā skin,Ā boneĀ andĀ theĀ brain

    Telomerase reverse transcriptase and telomeric-repeat binding factor protein 1 as regulators of telomerase activity in pancreatic cancer cells

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    Telomerase adds hexameric repeats of 5ā€²-TTAGGG-3ā€² termed telomeres to ends of chromosomal DNA. This enzyme has been implicated in cellular immortalization and cellular senescence. Recently, a number of relevant genes have been cloned, including these encoding three major components of human telomerase: human telomerase RNA component (hTR), human telomerase reverse transcriptase (hTERT), and telomerase-associated protein-1 (TEP1). Also important are genes encoding human telomeric-repeat binding factor protein (TRF) 1 and 2. To clarify mechanisms regulating telomerase activity, we studied telomerase activity, the telomeric restriction fragment (TRF) length and gene expression of these telomerase components and the telomeric-repeat binding factor proteins in sequential observation following X-irradiation of cultured pancreatic cancer cells. We previously reported that PANC-1 cells are better able to tolerate thermal stress, antineoplastic drugs, and exposure to tumour necrosis factor than MIAPaCa-2 cells. MIAPaCa-2 and PANC-1 cells were exposed to X-irradiation, their telomerase activity was increased at 2 days and then decreased gradually. Of the three telomerase components, only hTERT mRNA expression showed parallel changes. TRF length was stable just before and after X-irradiation. Among binding factor proteins, TRF1 mRNA showed reciprocal changes possibly directed toward maintaining a stable telomere length. In this study, our results demonstrate that not only hTERT but also TRF1 are important regulator of telomerase activity. Ā© 2001 Cancer Research Campaign http://www.bjcancer.co

    Native sulfur/chlorine SAD phasing for serial femtosecond crystallography

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    Serial femtosecond crystallography (SFX) allows structures to be determined with minimal radiation damage. However, phasing native crystals in SFX is not very common. Here, the structure determination of native lysozyme from single-wavelength anomalous diffraction (SAD) by utilizing the anomalous signal of sulfur and chlorine at a wavelength of 1.77 angstrom is successfully demonstrated. This sulfur SAD method can be applied to a wide range of proteins, which will improve the determination of native crystal structures.open112633sciescopu
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