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Quantification and Imaging of Antigens on Cell Surface with Lipid-Encapsulated Fluorescent Nanodiamonds

机译:脂质包裹的荧光纳米金刚石对细胞表面抗原的定量和成像

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摘要

Quantifying the density and locating the position of antigens on cell surface has been a challenge in molecular biology research. The challenge lies in the need for a chemically and photophysically stable fluorophore to achieve the required sensitivity and accuracy. Here, we present a method suitable for the purpose by using lipid-encapsulated fluorescent nanodiamonds (FNDs) of 35 nm in diameter as biolabels. The encapsulation of FNDs in biotinylated phospholipids not only facilitates good dispersion of the particles in biological buffers, but also endows them with high specific targeting ability. We demonstrated a viable application of the technique for biotin-mediated immunostaining of antigens on fixed human cells, identifying their positions by two-color confocal fluorescence imaging, and determining their densities by magnetically modulated fluorescence detection. A binding capacity of 6 ± 1 × 104 antigens/cell was measured specifically for CD44 on HeLa cell surface. The result agreed well with the assay of R-phycoerythrin-conjugated antibodies by flow cytometry, supporting the reliability of this new nanoparticle-based method.
机译:定量密度和定位抗原在细胞表面的位置一直是分子生物学研究的挑战。挑战在于需要一种化学和光物理稳定的荧光团,以实现所需的灵敏度和准确性。在这里,我们通过使用直径35 nm的脂质包裹的荧光纳米金刚石(FND)作为生物标记物,提出了一种适用于此目的的方法。 FNDs在生物素化磷脂中的包裹不仅促进了颗粒在生物缓冲液中的良好分散,而且赋予了它们较高的特异性靶向能力。我们证明了该技术在固定人细胞上生物素介导的抗原免疫染色,通过双色共聚焦荧光成像确定其位置并通过磁调制荧光检测确定其密度的技术的可行应用。对HeLa细胞表面的CD44的特异性结合能力为6±1×10 4 /细胞。结果与流式细胞仪检测R-藻红蛋白结合的抗体非常吻合,支持了这种新的基于纳米颗粒的方法的可靠性。

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