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Träfflista för sökning "WFRF:(Ignatenko N.) "

Sökning: WFRF:(Ignatenko N.)

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1.
  • Faatz, B., et al. (författare)
  • Simultaneous operation of two soft x-ray free-electron lasers driven by one linear accelerator
  • 2016
  • Ingår i: New Journal of Physics. - : IOP Publishing. - 1367-2630. ; 18
  • Tidskriftsartikel (refereegranskat)abstract
    • Extreme-ultraviolet to x-ray free-electron lasers (FELs) in operation for scientific applications are up to now single-user facilities. While most FELs generate around 100 photon pulses per second, FLASH at DESY can deliver almost two orders of magnitude more pulses in this time span due to its superconducting accelerator technology. This makes the facility a prime candidate to realize the next step in FELs-dividing the electron pulse trains into several FEL lines and delivering photon pulses to several users at the same time. Hence, FLASH has been extended with a second undulator line and self-amplified spontaneous emission (SASE) is demonstrated in both FELs simultaneously. FLASH can now deliver MHz pulse trains to two user experiments in parallel with individually selected photon beam characteristics. First results of the capabilities of this extension are shown with emphasis on independent variation of wavelength, repetition rate, and photon pulse length.
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2.
  • Strakova, A., et al. (författare)
  • Recurrent horizontal transfer identifies mitochondrial positive selection in a transmissible cancer
  • 2020
  • Ingår i: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 11
  • Tidskriftsartikel (refereegranskat)abstract
    • Autonomous replication and segregation of mitochondrial DNA (mtDNA) creates the potential for evolutionary conflict driven by emergence of haplotypes under positive selection for 'selfish' traits, such as replicative advantage. However, few cases of this phenomenon arising within natural populations have been described. Here, we survey the frequency of mtDNA horizontal transfer within the canine transmissible venereal tumour (CTVT), a contagious cancer clone that occasionally acquires mtDNA from its hosts. Remarkably, one canine mtDNA haplotype, A1d1a, has repeatedly and recently colonised CTVT cells, recurrently replacing incumbent CTVT haplotypes. An A1d1a control region polymorphism predicted to influence transcription is fixed in the products of an A1d1a recombination event and occurs somatically on other CTVT mtDNA backgrounds. We present a model whereby 'selfish' positive selection acting on a regulatory variant drives repeated fixation of A1d1a within CTVT cells.
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3.
  • Ekeberg, Tomas, 1983-, et al. (författare)
  • Observation of a single protein by ultrafast X-ray diffraction
  • 2024
  • Ingår i: Light. - : Springer Nature. - 2095-5545 .- 2047-7538. ; 13:1
  • Tidskriftsartikel (refereegranskat)abstract
    • The idea of using ultrashort X-ray pulses to obtain images of single proteins frozen in time has fascinated and inspired many. It was one of the arguments for building X-ray free-electron lasers. According to theory, the extremely intense pulses provide sufficient signal to dispense with using crystals as an amplifier, and the ultrashort pulse duration permits capturing the diffraction data before the sample inevitably explodes. This was first demonstrated on biological samples a decade ago on the giant mimivirus. Since then, a large collaboration has been pushing the limit of the smallest sample that can be imaged. The ability to capture snapshots on the timescale of atomic vibrations, while keeping the sample at room temperature, may allow probing the entire conformational phase space of macromolecules. Here we show the first observation of an X-ray diffraction pattern from a single protein, that of Escherichia coli GroEL which at 14 nm in diameter is the smallest biological sample ever imaged by X-rays, and demonstrate that the concept of diffraction before destruction extends to single proteins. From the pattern, it is possible to determine the approximate orientation of the protein. Our experiment demonstrates the feasibility of ultrafast imaging of single proteins, opening the way to single-molecule time-resolved studies on the femtosecond timescale.
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5.
  • Ignatenko, O. V., et al. (författare)
  • Electrochemistry of chemically trapped dimeric and monomeric recombinant horseradish peroxidase
  • 2013
  • Ingår i: Advances in Biosensors and Bioelectronics. - : Science and Engineering Publishing Company. - 2326-473X. ; 2:3, s. 25-34
  • Tidskriftsartikel (refereegranskat)abstract
    • Native horseradish peroxidase (nHRP) exists in the aggregated form in concentrated water solutions as shown by dynamic light scattering (DLS). This is in contrast to recombinant horseradish peroxidase (recHRP) which mainly exists as a dimer. The native enzyme aggregates could be broken into the particles of nm-size only under the conditions of high ionic strength (0.5-1 M NaCl). Chemical cross-linking of recHRP with glutaraldehyde in water solutions yields 40% of the dimer. The chemically trapped dimeric and monomeric forms of recHRP were separated by gel-filtration, their substrate specificity towards a number of organic substrates compared. Parameters of direct and mediated electron transfer on graphite electrodes catalyzed by both preparations were analyzed. The difference in behavior of the monomeric and dimeric enzyme forms observed in electrochemical experiments was interpreted as a result of a “double” coverage of the electrode surface with the molecules of cross-linked dimeric enzyme, in contrast to both modified monomeric and original, unmodified recHRP providing “monolayer” coverage. In addition to the stabilization effects achieved due to enzyme surface modification with glutaraldehyde, the “double” coverage doubles the enzyme activity per surface unit.
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