METU-MEMS Research and Application Center, Middle East Technical University (METU), Ankara, Turkey.
METU-MEMS Research and Application Center, Middle East Technical University (METU), Ankara, Turkey; Electrical and Electronics Engineering Department, Middle East Technical University (METU), Universiteler Mah., Dumlupinar Bulv. No: 1, 06800 Cankaya, Ankara, Turkey.
Biosens Bioelectron. 2014 Apr 15;54:27-34. doi: 10.1016/j.bios.2013.10.042. Epub 2013 Oct 31.
Glass microfibers are commonly used as biomolecule adsorption media, as structural or disposable components of the optical biosensors. While any improvement in these components are appreciated, utilizing basic tools of traditional approaches may lead to original sensor opportunities as simple, functional designs that can be easily disseminated. Following this pursuit, surface modification of glass microfiber paper surface was performed by 3-aminopropyltriethoxysilane (APTES) and resulting improvement in the cell entrapment capacity could be observed visually, only after Gram staining. Gram staining offered rapid validation of enhanced binding on the glass surface. The same APTES-modified samples were also tested for binding of complementary DNA sequences and the results were less straightforward due to the necessity of DNA visualization by using a fluorescent stain, YOYO-1. Accordingly, when there were no surface modification, DNA and YOYO-1 adsorbed readily on the glass microfiber filter paper, and prolonged the interaction between DNA and YOYO-1. YOYO-1 adsorption on glass could be recognized from the color profile of YOYO-1 emission. This phenomenon can be used to examine suitability of APTES coverage on glass surfaces since YOYO-1 emission can be distinguished by its glass adsorbed versus DNA-bound forms. Aptness of surface coverage is vital to biosensor studies in the sense that it is preceding the forthcoming surface modifications and its precision is imperative for attaining the anticipated interaction kinetics of the surface-immobilized species. The proposed testing scheme offered in this study secures the work, which is aimed to be carried out utilizing such sensing systems and device components.
玻璃微纤维通常被用作生物分子吸附介质,作为光学生物传感器的结构或一次性组件。虽然任何改进这些组件都值得赞赏,但利用传统方法的基本工具可能会带来原始传感器的机会,例如简单、功能的设计,可以很容易地传播。基于此追求,通过 3-氨丙基三乙氧基硅烷 (APTES) 对玻璃微纤维纸表面进行了表面修饰,只有在革兰氏染色后才能观察到细胞包埋能力的明显提高。革兰氏染色为玻璃表面增强结合提供了快速验证。同样的 APTES 修饰样品也被测试了与互补 DNA 序列的结合,结果并不那么直接,因为需要使用荧光染料 YOYO-1 来可视化 DNA。因此,当没有表面修饰时,DNA 和 YOYO-1 很容易吸附在玻璃微纤维滤纸上,并延长了 DNA 和 YOYO-1 之间的相互作用。玻璃上的 YOYO-1 吸附可以从 YOYO-1 发射的颜色轮廓中识别出来。这种现象可用于检查 APTES 在玻璃表面上的覆盖度是否合适,因为可以通过其玻璃吸附形式与 DNA 结合形式来区分 YOYO-1 发射。表面覆盖度的适宜性对于生物传感器研究至关重要,因为它是在即将进行的表面修饰之前进行的,其精度对于获得表面固定化物质的预期相互作用动力学至关重要。本研究中提出的测试方案确保了旨在利用这种传感系统和器件组件进行的工作。