CNR-IFN CSMFO Lab. and FBK CMM, via alla Cascata 56/C, 38123 Povo Trento, Italy.
FBK-LaBSSAH, via Sommarive 18, 38123 Povo Trento, Italy.
Sensors (Basel). 2018 Dec 7;18(12):4326. doi: 10.3390/s18124326.
In this paper, we described a versatile two steps approach for the realization of silica inverse opals functionalized with DNA-aptamers labelled with Cy3 fluorophore. The co-assembly method was successfully employed for the realization of high quality inverse silica opal, whilst the inverse network was functionalized via epoxy chemistry. Morphological and optical assessment revealed the presence of large ordered domains with a transmission band gap depth of 32%, after the functionalization procedure. Finite Difference Time-Domain (FDTD) simulations confirmed the high optical quality of the inverse opal realized. Photoluminescence measurements evidenced the effective immobilization of DNA-aptamer molecules labelled with Cy3 throughout the entire sample thickness. This assumption was verified by the inhibition of the fluorescence of Cy3 fluorophore tailoring the position of the photonic band gap of the inverse opal. The modification of the fluorescence could be justified by a variation in the density of states (DOS) calculated by the Plane Wave Expansion (PWE) method. Finally, the development of the aforementioned approach could be seen as proof of the concept experiment, suggesting that this type of system may act as a suitable platform for the realization of fluorescence-based bio-sensors.
在本文中,我们描述了一种通用的两步法,用于实现带有 Cy3 荧光团标记的 DNA 适体功能化的二氧化硅反蛋白石。共组装方法成功地用于实现高质量的反硅质蛋白石,而反网络则通过环氧化学进行功能化。形态和光学评估显示,在功能化后存在具有 32%传输带隙深度的大有序域。有限差分时域 (FDTD) 模拟证实了所实现的反蛋白石的高光学质量。光致发光测量证明了整个样品厚度内标记有 Cy3 的 DNA 适体分子的有效固定化。通过调整光子带隙的位置来抑制 Cy3 荧光团的荧光,证实了这一假设。通过平面波展开 (PWE) 方法计算的态密度 (DOS) 的变化可以解释荧光的变化。最后,上述方法的发展可以被视为概念实验的证明,表明这种类型的系统可以作为基于荧光的生物传感器的合适平台。