Cain Department of Chemical Engineering, Louisiana State University, 3307 Patrick F. Taylor Hall, Baton Rouge, LA, 70803, USA.
Anal Bioanal Chem. 2019 Jan;411(1):157-170. doi: 10.1007/s00216-018-1448-1. Epub 2018 Nov 28.
The use of high-throughput multiplexed screening platforms has attracted significant interest in the field of on-site disease detection and diagnostics for their capability to simultaneously interrogate single-cell responses across different populations. However, many of the current approaches are limited by the spectral overlap between tracking materials (e.g., organic dyes) and commonly used fluorophores/biochemical stains, thus restraining their applications in multiplexed studies. This work demonstrates that the downconversion emission spectra offered by rare earth (RE)-doped β-hexagonal NaYF nanoparticles (NPs) can be exploited to address this spectral overlap issue. Compared to organic dyes and other tracking materials where the excitation and emission is separated by tens of nanometers, RE elements have a large gap between excitation and emission which results in their spectral independence from the organic dyes. As a proof of concept, two differently doped NaYF NPs (europium: Eu, and terbium: Tb) were employed on a fluorescent microscopy-based droplet microfluidic trapping array to test their feasibility as spectrally independent droplet trackers. The luminescence tracking properties of Eu-doped (red emission) and Tb-doped (green emission) NPs were successfully characterized by co-encapsulating with genetically modified cancer cell lines expressing green or red fluorescent proteins (GFP and RFP) in addition to a mixed population of live and dead cells stained with ethidium homodimer. Detailed quantification of the luminescent and fluorescent signals was performed to confirm no overlap between each of the NPs and between NPs and cells. Thus, the spectral independence of Eu-doped and Tb-doped NPs with each other and with common fluorophores highlights the potential application of this novel technique in multiplexed systems, where many such luminescent NPs (other doped and co-doped NPs) can be used to simultaneously track different input conditions on the same platform. Graphical abstract ᅟ.
高通量多路复用筛选平台因其能够同时检测不同群体中单细胞的反应而在现场疾病检测和诊断领域引起了极大的兴趣。然而,许多当前的方法受到跟踪材料(例如有机染料)和常用荧光团/生化染色剂之间光谱重叠的限制,从而限制了它们在多路复用研究中的应用。这项工作表明,可以利用稀土(RE)掺杂的β-六方 NaYF 纳米粒子(NPs)的下转换发射光谱来解决这个光谱重叠问题。与有机染料和其他跟踪材料相比,激发和发射之间的距离相差数十纳米,而 RE 元素的激发和发射之间存在较大的间隙,这使得它们的光谱与有机染料无关。作为概念验证,两种不同掺杂的 NaYF NPs(铕:Eu 和铽:Tb)被用于基于荧光显微镜的液滴微流控捕获阵列上,以测试它们作为光谱独立的液滴跟踪器的可行性。通过共包封表达绿色或红色荧光蛋白(GFP 和 RFP)的基因修饰癌细胞系以及用 ethidium homodimer 染色的活细胞和死细胞的混合群体,成功地对 Eu 掺杂(红色发射)和 Tb 掺杂(绿色发射)NPs 的发光跟踪特性进行了表征。详细定量了发光和荧光信号,以确认每个 NPs 之间以及 NPs 与细胞之间没有重叠。因此,Eu 掺杂和 Tb 掺杂 NPs 之间以及它们与常见荧光团之间的光谱独立性突出了这项新技术在多路复用系统中的潜在应用,其中许多这样的发光 NPs(其他掺杂和共掺杂 NPs)可以用于同时跟踪同一平台上的不同输入条件。