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Reduced background autofluorescence for cell imaging using nanodiamonds and lanthanide chelates

机译:使用纳米金刚石和镧系元素螯合剂减少细胞成像的背景自发荧光

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摘要

Bio-imaging is a key technique in tracking and monitoring important biological processes and fundamental biomolecular interactions, however the interference of background autofluorescence with targeted fluorophores is problematic for many bio-imaging applications. This study reports on two novel methods for reducing interference with cellular autofluorescence for bio-imaging. The first method uses fluorescent nanodiamonds (FNDs), containing nitrogen vacancy centers. FNDs emit at near-infrared wavelengths typically higher than most cellular autofluorescence; and when appropriately functionalized, can be used for background-free imaging of targeted biomolecules. The second method uses europium-chelating tags with long fluorescence lifetimes. These europium-chelating tags enhance background-free imaging due to the short fluorescent lifetimes of cellular autofluorescence. In this study, we used both methods to target E-selectin, a transmembrane glycoprotein that is activated by inflammation, to demonstrate background-free fluorescent staining in fixed endothelial cells. Our findings indicate that both FND and Europium based staining can improve fluorescent bio-imaging capabilities by reducing competition with cellular autofluorescence. 30 nm nanodiamonds coated with the E-selectin antibody was found to enable the most sensitive detective of E-selectin in inflamed cells, with a 40-fold increase in intensity detected.
机译:生物成像是跟踪和监测重要的生物过程和基本生物分子相互作用的关键技术,但是,背景自发荧光对目标荧光团的干扰对于许多生物成像应用而言都是成问题的。这项研究报告了两种新颖的方法来减少对生物成像的细胞自发荧光的干扰。第一种方法使用包含氮空位中心的荧光纳米金刚石(FND)。 FND发射的近红外波长通常高于大多数细胞自发荧光。适当地功能化后,可用于目标生物分子的无背景成像。第二种方法使用荧光寿命长的euro螯合标签。这些cellular螯合标签由于细胞自体荧光的荧光寿命短而增强了无背景成像。在这项研究中,我们使用了两种方法来靶向E-选择素(一种被炎症激活的跨膜糖蛋白),以证明固定内皮细胞的无背景荧光染色。我们的发现表明,基于FND和Euro的染色均可通过减少与细胞自体荧光的竞争来提高荧光生物成像能力。发现用E-选择素抗体包被的30μnm纳米金刚石能够使发炎细胞中E-选择素的灵敏度最高,检测强度增加40倍。

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