首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Highly sensitive fluorescence biosensor for intracellular telomerase detection based on a single patchy gold/carbon nanosphere via the combination of nanoflare and hybridization chain reaction
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Highly sensitive fluorescence biosensor for intracellular telomerase detection based on a single patchy gold/carbon nanosphere via the combination of nanoflare and hybridization chain reaction

机译:高敏感的荧光生物传感器,用于细胞内端粒酶检测通过纳米缺陷和杂交链反应的组合基于单斑的金/碳纳米晶胞检测

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摘要

How to in situ detect intracellular telomerase activity with high sensitivity still faces many challenges. This paper constructs a new fluorescence biosensing platform for the sensitive detection of intracellular telomerase activity via the combination of nanoflare and hybridization chain reaction (HCR)-based signal amplification on a single patchy gold/carbon nanosphere (PG/CNS), which has two or more distinct parts and allows hybridized-DNA (HS-DNA/Primer-DNA/Flare-DNA) and Hl/H2-DNA (a pair of cross complementary DNA hairpins) to bind onto their surfaces via Au-S bond and electrostatic interaction, respectively. In the presence of telomerase, Primer-DNA (telomerase primer) extends at its 3' end to produce a telomeric repeated sequence, resulting in the release of Flare-DNA followed by the recovery of the fluorescence. Subsequently, the released Flare-DNA further initiates cross hybridization of H1 and H2 DNA from mimic-HCR system to amplify the fluorescence signal. The in vivo confocal microscopy studies demonstrate that resulting sensor can enter into the cancer cells such as A549 cells, and lead to the increase in luminescence, which is stronger than the sensor without the HCR-based signal amplification system. A linear relationship between the fluorescence intensity and the amount of A549 cells is observed, and the limit of detection of the sensor reaches about 280 A549 cells.
机译:如何原位检测细胞内端粒酶活性,具有高灵敏度仍面临许多挑战。本文构建了一种新的荧光生物传感平台,通过纳米缺陷和杂交链反应(HCR)的组合在单块斑块金/碳纳米(PG / CNS)上的纳米缺陷和杂交链反应(HCR)的信号放大来敏感检测细胞内端粒酶活性的敏感性检测。更明显的部分,允许杂交 - DNA(HS-DNA / PRIMER-DNA / FLARE-DNA)和HL / H2-DNA(一对交叉互补DNA发夹)通过AU-S键和静电相互作用将其结合到它们的表面上,分别。在端粒酶的存在下,引物-DNA(端粒酶引物)在其3'末端延伸以产生端粒重复序列,导致释放闪光DNA,然后释放荧光。随后,释放的FLARE-DNA进一步引发了来自模拟-HCR系统的H1和H 2 DNA的交叉杂交,以扩增荧光信号。体内共聚焦显微镜研究表明,所得传感器可以进入癌细胞,如A549细胞,导致发光的增加,这比没有基于HCR的信号放大系统的传感器更强。观察到荧光强度和A549细胞的量之间的线性关系,并且传感器的检测极限达到约280A549细胞。

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