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- Perriman, Adam W., et al.
(författare)
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Surface movement in water of splendipherin, the aquatic male sex pheromone of the tree frog Litoria splendida
- 2008
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Ingår i: The FEBS Journal. - : Wiley. - 1742-464X .- 1742-4658. ; 275:13, s. 3362-3374
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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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| 3. |
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| 4. |
- Abbott, Andrew, et al.
(författare)
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Ionic liquids at interfaces : general discussion
- 2018
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Ingår i: Faraday discussions. - : Royal Society of Chemistry (RSC). - 1359-6640 .- 1364-5498. ; 206, s. 549-586
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
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| 5. |
- Abraham, T., et al.
(författare)
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Polyelectrolyte-mediated interaction between similarly charged surfaces : Role of divalent counter ions in tuning surface forces
- 2001
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Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 17:26, s. 8321-8327
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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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| 8. |
- Álvarez-Asencio, Rubén, et al.
(författare)
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Nanomechanical properties of human skin and introduction of a novel hair indenter
- 2016
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Ingår i: Journal of The Mechanical Behavior of Biomedical Materials. - : Elsevier. - 1751-6161 .- 1878-0180. ; 54, s. 185-193
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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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| 9. |
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| 10. |
- Álvarez Asencio, Rubén, et al.
(författare)
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Nanotribology : Tribotronics, ionic liquids and control of surface interactions
- 2013
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Ingår i: 5th World Tribology Congress, WTC 2013. ; , s. 3106-3108
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Konferensbidrag (refereegranskat)abstract
- The interfacial ordering of Ionic liquids leads to interesting nanotribological properties as revealed by colloid probe studies. The first of these is the clear correlation between the number of ion pairs trapped in the tribological contact and the friction coefficient displayed. The second is the fact that the surface electrical potential can be used to control the composition of the boundary layer and thus tune the friction. Thirdly, the interfacial ordering appears to significantly affect the fluid dynamics over large distances.
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