Institute of Chemistry for Life and Health Sciences i-CLeHS, Chimie ParisTech-PSL/CNRS 8060 , Paris, France.
Instituto de Química, Universidade Federal de Goiás, Goiânia, Brazil.
Electrophoresis. 2022 Oct;43(20):2044-2048. doi: 10.1002/elps.202200057. Epub 2022 Aug 10.
A low-cost and straightforward hybrid NOA (Norland optical adhesive) 81-glass microchip electrophoresis device was designed and developed for protein separation using indirect fluorescence detection. This new microchip was first characterized in terms of surface charge density via electroosmotic mobility measurement and stability over time. A systematic determination of the electroosmotic mobility (μ ) over a wide pH range (2-10) and at various ionic strengths (20-50 mM) was developed for the first time via the neutral marker approach in an original simple frontal methodology. The evolution of μ was proved consistent with the silanol and thiol functions arising from the glass and the NOA materials, respectively. The repeatability and reproducibility of the measurements on different microchips (RSD < 14%) and within 15 days (less than 5% decrease) were successfully demonstrated. The microchip was then applied for the efficient electrophoretic separation of proteins in a zonal mode coupled with indirect fluorescence detection, which is, to our knowledge, the first proof of concept of capillary zone electrophoresis in this hybrid microsystem.
设计并开发了一种低成本、简单的混合 NOA(诺兰光学胶)81 玻璃微芯片电泳装置,用于使用间接荧光检测进行蛋白质分离。首次通过电渗流迁移率测量和随时间的稳定性来对这种新微芯片的表面电荷密度进行了表征。首次通过中性标记法在原始简单的前沿方法中,在很宽的 pH 范围(2-10)和不同的离子强度(20-50 mM)下系统地确定了电渗流迁移率(μ)。μ的变化与玻璃和 NOA 材料分别产生的硅烷醇和硫醇官能团一致。成功证明了在不同微芯片上(RSD < 14%)和 15 天内(小于 5%的下降)测量的重复性和再现性。然后,该微芯片被应用于在带有间接荧光检测的带状模式下进行蛋白质的有效电泳分离,据我们所知,这是在这种混合微系统中首次证明毛细管区带电泳的概念。