277 research outputs found
Diffraction from the beta-sheet crystallites in spider silk
We analyze the wide angle x-ray scattering from oriented spider silk fibers
in terms of a quantitative scattering model, including both structural and
statistical parameters of the -sheet crystallites of spider silk in the
amorphous matrix. The model is based on kinematic scattering theory and allows
for rather general correlations of the positional and orientational degrees of
freedom, including the crystallite's size, composition and dimension of the
unit cell. The model is evaluated numerically and compared to experimental
scattering intensities allowing us to extract the geometric and statistical
parameters. We show explicitly that for the experimentally found mosaicity
(width of the orientational distribution) inter-crystallite effects are
negligible and the data can be analyzed in terms of single crystallite
scattering, as is usually assumed in the literature.Comment: 15 pages, 14 figures, on average 0.93 figures per pag
Anomalous X-ray scattering at the sulfur edge of poly(3-octylthiophene)
Anomalous X-ray diffraction was performed at the sulfur K edge of the partially crystalline conducting polymer poly(3-octylthiophene) (P3OT). This is the first time anomalous diffraction at the sulfur edge has been used to obtain additional information on the structure of a polymer. A strong wavelength intensity variation of the 100 reflection was observed. This intensity change and the variation of the fluorescent scattered background corroborate excellently with the theory and theoretical intensity calculations confirm previously suggested structural models
Microfluidics: From Crystallization to Serial Time-Resolved Crystallography
Capturing protein structural dynamics in real-time has tremendous potential in elucidating biological functions and providing information for structure-based drug design. While time-resolved structure determination has long been considered inaccessible for a vast majority of protein targets, serial methods for crystallography have remarkable potential in facilitating such analyses. Here, we review the impact of microfluidic technologies on protein crystal growth and X-ray diffraction analysis. In particular, we focus on applications of microfluidics for use in serial crystallography experiments for the time-resolved determination of protein structural dynamics
Characterization of activated carbon fiber/polyaniline materials by position-resolved microbeam small-angle X-ray scattering
Activated carbon fiber (ACF)/polyaniline (PANI) materials have been prepared using two different methods, viz. chemical and electrochemical polymerization. Electrochemical characterization of both materials shows that the electrodes with polyaniline have a higher capacitance than does a pristine porous carbon electrode. To analyze the distribution of PANI within the ACF, characterization by position-resolved microbeam small-angle X-ray scattering (μSAXS) has been carried out. μSAXS results obtained with a single ACF indicate that, for the experimental conditions used, a PANI coating is formed inside the micropores and that it is higher in the external regions of the ACF than in the core. Additionally, it seems that the penetration of PANI inside the fibers occurs in a larger extent for the chemical polymerization or, in other words, for the electrochemically polymerized sample there is a slightly larger accumulation of PANI in the external regions of the ACF.Fil: Salinas-Torres, D.. Universida de Alicante; EspañaFil: Sieben, Juan Manuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; ArgentinaFil: Lozano-Castelló, D.. Universida de Alicante; EspañaFil: Morallón, E.. Universida de Alicante; EspañaFil: Burghammer, M.. EuropeanSynchrotronRadiationFacility; FranciaFil: Riekel, C.. EuropeanSynchrotronRadiationFacility; FranciaFil: Cazorla Amorós, Diego. Universida de Alicante; Españ
Large Thermoelectric Power Factor in TiS2 Crystal with Nearly Stoichiometric Composition
A TiS crystal with a layered structure was found to have a large
thermoelectric power factor.The in-plane power factor at 300 K is
37.1~W/Kcm with resistivity () of 1.7 mcm and
thermopower () of -251~V/K, and this value is comparable to that of the
best thermoelectric material, BiTe alloy. The electrical
resistivity shows both metallic and highly anisotropic behaviors, suggesting
that the electronic structure of this TiS crystal has a
quasi-two-dimensional nature. The large thermoelectric response can be ascribed
to the large density of state just above the Fermi energy and inter-valley
scattering. In spite of the large power factor, the figure of merit, of
TiS is 0.16 at 300 K, because of relatively large thermal conductivity,
68~mW/Kcm. However, most of this value comes from reducible lattice
contribution. Thus, can be improved by reducing lattice thermal
conductivity, e.g., by introducing a rattling unit into the inter-layer sites.Comment: 11 pages, 4 figures, to be published in Physical Review
Protein crystallography with a micrometre-sized synchrotron-radiation beam
For the first time, protein microcrystallography has been performed with a focused synchrotron-radiation beam of 1 µm using a goniometer with a sub-micrometre sphere of confusion. The crystal structure of xylanase II has been determined with a flux density of about 3 × 1010 photons s−1 µm−2 at the sample
Identification and dynamics of polyglycine II nanocrystals in Argiope trifasciata flagelliform silk
Spider silks combine a significant number of desirable characteristics in one material, including large tensile strength and strain at breaking, biocompatibility, and the possibility of tailoring their properties. Major ampullate gland silk (MAS) is the most studied silk and their properties are explained by a double lattice of hydrogen bonds and elastomeric protein chains linked to polyalanine β-nanocrystals. However, many basic details regarding the relationship between composition, microstructure and properties in silks are still lacking. Here we show that this relationship can be traced in flagelliform silk (Flag) spun by Argiope trifasciata spiders after identifying a phase consisting of polyglycine II nanocrystals. The presence of this phase is consistent with the dominant presence of the –GGX– and –GPG– motifs in its sequence. In contrast to the passive role assigned to polyalanine nanocrystals in MAS, polyglycine II nanocrystals can undergo growing/collapse processes that contribute to increase toughness and justify the ability of Flag to supercontract
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