State Key Laboratory of NBC Protection for Civilian, Beijing, 102205, China.
State Key Laboratory of NBC Protection for Civilian, Beijing, 102205, China.
Talanta. 2023 Aug 1;260:124563. doi: 10.1016/j.talanta.2023.124563. Epub 2023 Apr 18.
Aiming for precise, real-time, and on-site analysis of proteins, an innovative binary-emission fluorescence imprinted polymer was designed by sol-gel method after mixing MIL-101(Cr), green CdTe (g-CdTe) and red CdTe (r-CdTe) for detection of protein. In this proposal, MIL-101(Cr), as a favorable supporter, provided high surface area and porosity for imprinting sites, which ameliorated the transfer rate and the sensitivity of the nanosensor. And g-CdTe and r-CdTe were served as signal transduction for dual-emission response. Based on strengthened recognition reaction between high-affinity imprinting sites and protein, the fluorescence intensities of g-CdTe and r-CdTe yielded conspicuous two responses at 528 nm and 634 nm for protein under the excitation of 350 nm. The cytochrome c (Cyt c) and trypsin were served as model proteins to verify the generality of strategy. Given prominent merits of MIL-101(Cr), g-CdTe/r-CdTe@MIL-101(Cr)@MIP exhibited good linear range of 1-30 μM for Cyt c and 0.15-4 μM for trypsin, and the limit of detection were 0.13 μM and 0.014 μM, respectively. Significantly, an unsophisticated smartphone-based sensing device was developed by integrating g-CdTe/r-CdTe@MIL-101(Cr)@MIP with a 3D printing portable device to obtain precise on-site results. As expected, this portable platform was successfully applied for monitoring Cyt c and trypsin with a detection limit of 0.71 μM and 0.026 μM, respectively. These results indicated this dual-response molecularly imprinted fluorescence senor based on smartphone provided promising perspectives on futural on-site protein analysis.
为了实现对蛋白质的精确、实时和现场分析,本研究通过溶胶-凝胶法设计了一种创新的双发射荧光印迹聚合物,该聚合物混合了 MIL-101(Cr)、绿色 CdTe(g-CdTe)和红色 CdTe(r-CdTe),用于蛋白质检测。在该方案中,MIL-101(Cr)作为有利的载体,为印迹位点提供了高的表面积和孔隙率,改善了纳米传感器的传输速率和灵敏度。g-CdTe 和 r-CdTe 则作为双发射响应的信号转导。基于高亲和力印迹位点与蛋白质之间的增强识别反应,在 350nm 激发下,蛋白质的荧光强度在 528nm 和 634nm 处产生明显的两个响应。细胞色素 c(Cyt c)和胰蛋白酶被用作模型蛋白来验证该策略的通用性。鉴于 MIL-101(Cr)的突出优点,MIL-101(Cr)@MIP 显示出对 Cyt c 的良好线性范围为 1-30μM,对胰蛋白酶的线性范围为 0.15-4μM,检测限分别为 0.13μM 和 0.014μM。值得注意的是,通过将 g-CdTe/r-CdTe@MIL-101(Cr)@MIP 与 3D 打印便携式设备集成,开发了一种简单的基于智能手机的传感装置,以获得精确的现场结果。不出所料,该便携式平台成功地用于监测 Cyt c 和胰蛋白酶,检测限分别为 0.71μM 和 0.026μM。这些结果表明,基于智能手机的这种双响应分子印迹荧光传感器为未来的现场蛋白质分析提供了有前景的前景。