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Autor(en) / Beteiligte
Titel
QCM sensing of multivalent interactions between lectins and well-defined glycosylated nanoplatforms
Ist Teil von
  • Biosensors & bioelectronics, 2019-08, Vol.139, p.111328, Article 111328
Ort / Verlag
England: Elsevier B.V
Erscheinungsjahr
2019
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Quartz crystal microbalance (QCM) methodology has been adopted to unravel important factors contributing to the “cluster glycoside effect” observed in carbohydrate-lectin interactions. Well-defined, glycosylated nanostructures of precise sizes, geometries and functionalization patterns were designed and synthesized, and applied to analysis of the interaction kinetics and thermodynamics with immobilized lectins. The nanostructures were based on Borromean rings, dodecaamine cages, and fullerenes, each of which carrying a defined number of carbohydrate ligands at precise locations. The synthesis of the Borromeates and dodecaamine cages was easily adjustable due to the modular assembly of the structures, resulting in variations in presentation mode. The binding properties of the glycosylated nanoplatforms were evaluated using flow-through QCM technology, as well as hemagglutination inhibition assays, and compared with dodecaglycosylated fullerenes and a monovalent reference. With the QCM setup, the association and dissociation rate constants and the associated equilibrium constants of the interactions could be estimated, and the results used to delineate the multivalency effects of the lectin-nanostructure interactions. [Display omitted] •QCM can be used to delineate multivalency effects in carbohydrate-lectin interactions.•Well-defined, precisely glycosylated nanoplatforms of various symmetry, charge and size are important tools to probe the “cluster glycoside effect”.•Optimal carbohydrate distribution patterns are essential to obtain high affinities, in combination with matching polyelectrolyte effects.
Sprache
Englisch
Identifikatoren
ISSN: 0956-5663, 1873-4235
eISSN: 1873-4235
DOI: 10.1016/j.bios.2019.111328
Titel-ID: cdi_swepub_primary_oai_DiVA_org_lnu_86911

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