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Sökning: WFRF:(Rutland Mark W.)

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1.
  • Perriman, Adam W., et al. (författare)
  • Surface movement in water of splendipherin, the aquatic male sex pheromone of the tree frog Litoria splendida
  • 2008
  • Ingår i: The FEBS Journal. - : Wiley. - 1742-464X .- 1742-4658. ; 275:13, s. 3362-3374
  • Tidskriftsartikel (refereegranskat)abstract
    • The aquatic sex pheromone splendipherin (GLVSSIGKALGGLLADVVKSKGQPA-OH) of the male green tree frog Litoria splendida moves across the surface of water to reach the female. Surface pressure and X-ray reflectometry measurements confirm that splendipherin is a surface-active molecule, and are consistent with it having an ordered structure, whereby the hydrophilic portion of the peptide interacts with the underlying water and the hydrophobic region is adjacent to the vapour phase. The movement of splendipherin over the surface of water is caused by a surface pressure gradient. In order to better define the structure of splendipherin at the water/air interface we used 2D NMR studies of the pheromone with the solvent system trifluoroethanol/water (1 : 1 v/v). In this solvent system, splendipherin adopts a bent alpha helix from residues V3 to K21. The bending of the helix occurs in the centre of the peptide in the vicinity of G11 and G12. The region of splendipherin from V3 to G11 has well-defined amphipathicity, whereas the amphipathicity from G12 to A25 is reduced by K19 and P24 intruding into the hydrophobic and hydrophilic regions respectively. A helical structure is consistent with X-ray reflectometry data.
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4.
  • Rutland, Mark W., et al. (författare)
  • Analysis of atomic force microscopy data for deformable materials
  • 2004
  • Ingår i: Journal of Adhesion Science and Technology. - : Informa UK Limited. - 0169-4243 .- 1568-5616. ; 18:10, s. 1199-1215
  • Tidskriftsartikel (refereegranskat)abstract
    • A protocol for measuring the interaction, deformation and adhesion of soft polymeric substrates with the atomic force microscope (AFM) is described. The technique obtains the photodiode response of the AFM (constant compliance factor) by independent calibration against the rigid substrate adjacent to the deformable particle or patchy film. The zero of separation is taken as the end-point of the jump into contact. A method is given for correcting the velocity dependence of the piezodrive expansion factor, the neglect of which will cause artefacts in dynamic viscoelastic measurements. It is emphasised that conventional force curve analysis, which uses the apparently linear large force region for calibration, will generate erroneous results for deformable substrates. Results are obtained for cellulose particles and for polystyrene films, and their Young's moduli are found to be 22 MPa and 100 MPa, respectively. The latter is about a factor of 30 less than for bulk polystyrene, which indicates that the polystyrene surface is in a less glassy state than the bulk.
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5.
  • Sörensen, Malin H., et al. (författare)
  • AFM-Porosimetry : Density and pore volume measurements ofparticulate materials
  • 2008
  • Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 24, s. 7024-7030
  • Tidskriftsartikel (refereegranskat)abstract
    • We introduced the novel technique of AFM-porosimetry and applied it to measure the total pore volume of porous particles with a spherical geometry. The methodology is based on using an atomic force microscope as a balance to measure masses of individual particles. Several particles within the same batch were measured, and by plotting particle mass versus particle volume, the bulk density of the sample can be extracted from the slope of the linear fit. The pore volume is then calculated from the densities of the bulk and matrix materials, respectively. In contrast to nitrogen sorption and mercury porosimetry, this method is capable of measuring the total pore volume regardless of pore size distribution and pore connectivity. In this study, three porous samples were investigated by AFM-porosimetry: one ordered mesoporous sample and two disordered foam structures. All samples were based on a matrix of amorphous silica templated by a block copolymer, Pluronic F127, swollen to various degrees with poly(propylene glycol). In addition, the density of silica spheres without a template was measured by two independent techniques: AFM and the Archimedes principle.
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6.
  • Abbott, Andrew, et al. (författare)
  • Ionic liquids at interfaces : general discussion
  • 2018
  • Ingår i: Faraday discussions. - : Royal Society of Chemistry (RSC). - 1359-6640 .- 1364-5498. ; 206, s. 549-586
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
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7.
  • Abraham, T., et al. (författare)
  • Polyelectrolyte-mediated interaction between similarly charged surfaces : Role of divalent counter ions in tuning surface forces
  • 2001
  • Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 17:26, s. 8321-8327
  • Tidskriftsartikel (refereegranskat)abstract
    • The effects of divalent salts (CaCl2, MgCl2 and BaCl2) in promoting the adsorption of weakly charged polyelectrolyte (polyacrylic acid), PAA, Mw similar to 250000 g/mol) on mica surfaces and their role in tuning the nature of interactions between such adsorbed polyelectrolyte layers were studied using the interferometric surface forces apparatus. With mica surfaces in 3 mM MgCl2 solutions at pH similar to8.0-9.0, the addition of 10 ppm PAA resulted in a long-range attractive bridging force and a short-range repulsive steric force. This force profile indicates a low surface coverage and weak adsorption. The range of the force can be related to the characteristic length scale R-G of polyelectrolyte chains using a scaling description. An increase of the PAA concentration to 50 ppm changed the attractive force profile to a monotonic, long-range repulsive interaction extending up to 600 Angstrom due to the increased surface coverage of polyelectrolyte chains on the mica surfaces. Comparison of the measured forces with a scaling mean field model suggests that the adsorbed polyelectrolyte chains are stretched, which eventually give rise to the polyelectrolyte brush like structure. When the mica surfaces were preincubated in 3 mM CaCl2 at pH similar to8.0-9.0, in contrast to the case of 3 MM MgCl2, the addition of 10 ppm PAA resulted in a more complex force profile: long-range repulsive forces extending up to 800 Angstrom followed by an attractive force regime and a second repulsive force regime at shorter separations. The long-range electrosteric forces can be attributed to strong adsorption of polyelectrolyte chains on mica surfaces (high surface coverage) which is facilitated by the presence of Ca2+ ions, while the intermediate range attractive forces can be ascribed to Ca2+ assisted bridging between adsorbed polyelectrolyte chains. Also interesting is to note various relaxation processes present in this system. In contrast to both MgCl2 and CaCl2 systems, with mica surfaces in 3 mM BaCl2 solution at pH similar to8.0-9.0, the addition of 10 ppm PAA resulted in precipitation of polyelectrolyte chains on mica surfaces, resulting in an extremely long-range monotonic repulsive force profile. In summary, our study showed that divalent counterions (Mg2+, Ca2+, and Ba2+) exhibit significantly different behavior in promoting PAA adsorption on mica surfaces, modifying and controlling various surface interactions.
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  • Álvarez-Asencio, Rubén, et al. (författare)
  • Nanomechanical properties of human skin and introduction of a novel hair indenter
  • 2016
  • Ingår i: Journal of The Mechanical Behavior of Biomedical Materials. - : Elsevier. - 1751-6161 .- 1878-0180. ; 54, s. 185-193
  • Tidskriftsartikel (refereegranskat)abstract
    • The mechanical resistance of the stratum corneum, the outermost layer of skin, to deformation has been evaluated at different length scales using Atomic Force Microscopy. Nanomechanical surface mapping was first conducted using a sharp silicon tip and revealed that Young’s modulus of the stratum corneum varied over the surface with a mean value of about 0.4 GPa. Force indentation measurements showed permanent deformation of the skin surface only at high applied loads (above 4 μN). The latter effect was further demonstrated using nanomechanical imaging in which the obtained depth profiles clearly illustrate the effects of increased normal force on the elastic/plastic surface deformation. Force measurements utilizing the single hair fiber probe supported the nanoindentation results of the stratum corneum being highly elastic at the nanoscale, but revealed that the lateral scale of the deformation determines the effective elastic modulus.This result resolves the fact that the reported values in the literature vary greatly and will help to understand the biophysics of the interaction of razor cut hairs that curl back during growth and interact with the skin.
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