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Single‐Nanoparticle Cell Barcoding by Tunable FRET from Lanthanides to Quantum Dots

机译:可调谐FRET从镧系元素到量子点的单纳米颗粒细胞条形码

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摘要

Fluorescence barcoding based on nanoparticles provides many advantages for multiparameter imaging. However, creating different concentration‐independent codes without mixing various nanoparticles and by using single‐wavelength excitation and emission for multiplexed cellular imaging is extremely challenging. Herein, we report the development of quantum dots (QDs) with two different SiO2 shell thicknesses (6 and 12 nm) that are coated with two different lanthanide complexes (Tb and Eu). FRET from the Tb or Eu donors to the QD acceptors resulted in four distinct photoluminescence (PL) decays, which were encoded by simple time‐gated (TG) PL intensity detection in three individual temporal detection windows. The well‐defined single‐nanoparticle codes were used for live cell imaging and a one‐measurement distinction of four different cells in a single field of view. This single‐color barcoding strategy opens new opportunities for multiplexed labeling and tracking of cells.
机译:基于纳米粒子的荧光条形码为多参数成像提供了许多优势。但是,在不混合各种纳米粒子的情况下创建不同的浓度无关代码,以及通过使用单波长激发和发射进行多路细胞成像是非常具有挑战性的。在这里,我们报道了具有两种不同的SiO2壳厚度(6和12 nm)的量子点(QDs)的发展,该壳层被两种不同的镧系元素络合物(Tb和Eu)包覆。从Tb或Eu供体到QD受体的FRET导致四个不同的光致发光(PL)衰减,这些衰减通过在三个独立的时间检测窗口中通过简单的时间门控(TG)PL强度检测进行编码。定义明确的单纳米粒子代码用于活细胞成像,并在单个视野中对四个不同细胞进行一次测量区分。这种单色条形码策略为细胞的多重标记和跟踪带来了新的机会。

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