Tannin-on-protein adlayers: Secondary adsorption quantified by quartz crystal microbalance with dissipation monitoring (QCM-D)

被引:2
|
作者
Larcinese-Hafner, Valeria [1 ]
Erni, Philipp [1 ]
机构
[1] Formulat & Mat Sci Dept, Sci & Res Div, DSM Firmenich, 7 Rue Bergere, CH-1242 Geneva, Switzerland
关键词
BETA-LACTOGLOBULIN ADSORPTION; HYDROLYZABLE TANNINS; SALIVARY PROTEINS; CONDENSED TANNINS; ASTRINGENCY; BINDING; GRAPE; PRECIPITATION; ELECTROPHORESIS; PROCYANIDINS;
D O I
10.1016/j.foodhyd.2024.110443
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The quartz crystal microbalance with dissipation monitoring (QCM-D) technique allows to detect adsorption and mechanical characteristics of protein adsorption layers at solid surfaces, including subsequent secondary adsorption of additional species interacting with the proteins. Here, we study the secondary adsorption of two different classes of tannins- hydrolysable vs. condensed- onto a beta- lactoglobulin base layer using QCM-D in a protein/tannin adlayer configuration. Sequential flow experiments of protein solutions, tannin solutions and neat solvent or buffer are used to distinguish reversible from desorption-resistant layer formation, evaluate the viscoelastic characteristics the layers, and map protein/tannin interactions in view of their structural properties and origin. We find that for the majority of tannins, secondary layer structural changes (detected via a change in the dissipation factor) occur before significant mass adsorption (detected via the resonance frequency shift). In contrast, simultaneous onset of structural change and adsorbed mass within an observation window of 100 ms was only found for certain hydrolysable tannins. We use these data to build adsorption maps and group the tannins according to their adlayer properties, providing a physical basis for an improved understanding of the organoleptic perception of tannins and polyphenols, in particular with respect to attributes such as 'astringency' and 'lingering'. Moreover, these maps provide insight into the capacity of different tannins to modify the mechanical properties of protein adsorption layers.
引用
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页数:11
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