Publications by authors named "G C Sanderson"

Article Synopsis
  • Researchers captured tiny oil droplets using a polymer brush made from a hydrophilic aldehyde-functional material.
  • The brush was created through a specific polymerization process and modified to add aldehyde groups.
  • The study shows that these nanosized droplets can bind to the polymer brush through chemical bonds, which can be adjusted by altering the pH of the solution, providing insights into oil droplet behavior on soft surfaces.
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Article Synopsis
  • * Recent advancements involve using a pump beam to enhance signal conversion via four-wave mixing (FWM), focusing on resonances at the pump wavelength to achieve better nonlinear imaging.
  • * This approach allows for broadband nonlinear imaging across a wide infrared range (1000-4000 nm) with metasurfaces, representing a significant improvement for future compact photonic devices in all-optical infrared imaging.
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Compared to lipids, block copolymer vesicles are potentially robust nanocontainers for enzymes owing to their enhanced chemical stability, particularly in challenging environments. Herein we report that -diol-functional diblock copolymer vesicles can be chemically adsorbed onto a hydrophilic aldehyde-functional polymer brush via acetal bond formation under mild conditions (pH 5.5, 20 °C).

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Ferritin, a spherical protein shell assembled from 24 subunits, functions as an efficient iron storage and release system through its channels. Understanding how various chemicals affect the structural behavior of ferritin is crucial for unravelling the origins of iron-related diseases in living organisms including humans. In particular, the influence of chemicals on ferritin's dynamics and iron release is barely explored at the single-protein level.

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Recently, we reported the synthesis of a hydrophilic aldehyde-functional methacrylic polymer (, , , 12032-12037). Herein we demonstrate that such polymers can be reacted with arginine in aqueous solution to produce arginine-functional methacrylic polymers without recourse to protecting group chemistry. Careful control of the solution pH is essential to ensure regioselective imine bond formation; subsequent reductive amination leads to a hydrolytically stable amide linkage.

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