4 results match your criteria: "University of Warwick CV4 7AL UK.[Affiliation]"

Cryopreservation is crucial to fields including immune and stem cell therapies, reproductive technology, blood banking, regenerative medicine and across all biotechnology. During cryopreservation, cryoprotectants are essential to protect cells from the damage caused by exposure to freezing temperatures. The most common penetrating cryoprotectants, such as DMSO and glycerol do not give full recovery and have a cytotoxicity limit on the concentration which can be applied.

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Article Synopsis
  • - Glycan-lectin interactions are critical in biological processes like pathogen attachment and immune response, but current methods to study these interactions are often expensive and not widely accessible.
  • - Recently developed glycosylated plasmonic nanoparticles offer a cost-effective biosensor alternative that detects glycan-protein binding through noticeable color changes, which can be analyzed with simple equipment.
  • - This research suggests optimal parameters (gold core size and polymer tether length) for using these nanoparticles, allowing lab users to efficiently investigate new glycan/protein interactions with minimal optimization needed.
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Hyaluronic acid (HA), the only non-sulphated glycosaminoglycan, serves numerous structural and biological functions in the human body, from providing viscoelasticity in tissues to creating hydrated environments for cell migration and proliferation. HA is also involved in the regulation of morphogenesis, inflammation and tumorigenesis through interactions with specific HA-binding proteins. Whilst the physicochemical and biological properties of HA have been widely studied for decades, the exact mechanisms by which HA exerts its multiple functions are not completely understood.

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Galectins are potential biomarkers and therapeutic targets. However, galectins display broad affinity towards β-galactosides meaning glycan-based (nano)biosensors lack the required selectivity and affinity. Using a polymer-stabilized nanoparticle biosensing platform, we herein demonstrate that the specificity of immobilised lacto--biose towards galectins can be 'turned on/off' by using site-specific glycan fluorination and in some cases reversal of specificity can be achieved.

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