Voltammetric behaviour of biological macromolecules at arrays of aqueous|organogel micro-interfaces

The behaviour of two biological macromolecules, bovine pancreatic insulin and hen-egg-whitelysozyme (HEWL), at aqueous-organogel interfaces confined within an array of solid-state membrane micropores was investigated via cyclic voltammetry (CV). The behaviour observed is discussed in terms of possib...

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Main Authors: Scanlon, M., Strutwolf, J., Arrigan, Damien
Format: Journal Article
Published: Royal Society of Chemistry 2010
Online Access:http://hdl.handle.net/20.500.11937/26812
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author Scanlon, M.
Strutwolf, J.
Arrigan, Damien
author_facet Scanlon, M.
Strutwolf, J.
Arrigan, Damien
author_sort Scanlon, M.
building Curtin Institutional Repository
collection Online Access
description The behaviour of two biological macromolecules, bovine pancreatic insulin and hen-egg-whitelysozyme (HEWL), at aqueous-organogel interfaces confined within an array of solid-state membrane micropores was investigated via cyclic voltammetry (CV). The behaviour observed is discussed in terms of possible charge transferring species and mass transport in the interfacial reaction. Comparison of CV results for HEWL, insulin, and the well-characterised model ion tetraethylammonium cation (TEA+) revealed that the biomacromolecules undergo an interfacial reaction comprising biomacromolecular adsorption and facilitated transfer of electrolyte anions from the organic phase to a protein layer on the aqueous side of the interface, whereas TEA+ undergoes a simple ion transfer process. Evidence for biomacromolecular adsorption on the aqueous side of the micro-interfaces is provided by comparison of the CVs for TEA+ ion transfer in the presence and absence of the biomacromolecules. Similar experiments in the presence of the low generation polypropylenimine tetraamine dendrimer, (DAB-AM-4), a smaller synthetic molecule, revealed it to be non-adsorbing. The behaviour of biological macromolecules at miniaturised aqueous-organogel interfaces involves adsorption on the aqueous side of the interface and transfer of organic phase electrolyte anions across the interface to associate with the adsorbed biomacro molecule. The data presented support the previously suggested mechanism forbiomacromolecular voltammetry at liquid-liquid interfaces, involving adsorption and facilitated ion-transfer of organic electrolyte anions.
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institution Curtin University Malaysia
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publishDate 2010
publisher Royal Society of Chemistry
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spelling curtin-20.500.11937-268122017-10-02T02:28:22Z Voltammetric behaviour of biological macromolecules at arrays of aqueous|organogel micro-interfaces Scanlon, M. Strutwolf, J. Arrigan, Damien The behaviour of two biological macromolecules, bovine pancreatic insulin and hen-egg-whitelysozyme (HEWL), at aqueous-organogel interfaces confined within an array of solid-state membrane micropores was investigated via cyclic voltammetry (CV). The behaviour observed is discussed in terms of possible charge transferring species and mass transport in the interfacial reaction. Comparison of CV results for HEWL, insulin, and the well-characterised model ion tetraethylammonium cation (TEA+) revealed that the biomacromolecules undergo an interfacial reaction comprising biomacromolecular adsorption and facilitated transfer of electrolyte anions from the organic phase to a protein layer on the aqueous side of the interface, whereas TEA+ undergoes a simple ion transfer process. Evidence for biomacromolecular adsorption on the aqueous side of the micro-interfaces is provided by comparison of the CVs for TEA+ ion transfer in the presence and absence of the biomacromolecules. Similar experiments in the presence of the low generation polypropylenimine tetraamine dendrimer, (DAB-AM-4), a smaller synthetic molecule, revealed it to be non-adsorbing. The behaviour of biological macromolecules at miniaturised aqueous-organogel interfaces involves adsorption on the aqueous side of the interface and transfer of organic phase electrolyte anions across the interface to associate with the adsorbed biomacro molecule. The data presented support the previously suggested mechanism forbiomacromolecular voltammetry at liquid-liquid interfaces, involving adsorption and facilitated ion-transfer of organic electrolyte anions. 2010 Journal Article http://hdl.handle.net/20.500.11937/26812 10.1039/c003323e Royal Society of Chemistry fulltext
spellingShingle Scanlon, M.
Strutwolf, J.
Arrigan, Damien
Voltammetric behaviour of biological macromolecules at arrays of aqueous|organogel micro-interfaces
title Voltammetric behaviour of biological macromolecules at arrays of aqueous|organogel micro-interfaces
title_full Voltammetric behaviour of biological macromolecules at arrays of aqueous|organogel micro-interfaces
title_fullStr Voltammetric behaviour of biological macromolecules at arrays of aqueous|organogel micro-interfaces
title_full_unstemmed Voltammetric behaviour of biological macromolecules at arrays of aqueous|organogel micro-interfaces
title_short Voltammetric behaviour of biological macromolecules at arrays of aqueous|organogel micro-interfaces
title_sort voltammetric behaviour of biological macromolecules at arrays of aqueous|organogel micro-interfaces
url http://hdl.handle.net/20.500.11937/26812