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通过无信号放大策略,基于 DNA 诱导碳点在金纳米粒子上的组装实现对 microRNA 的超灵敏荧光检测。

Ultrasensitive fluorescence detection of microRNA through DNA-induced assembly of carbon dots on gold nanoparticles with no signal amplification strategy.

机构信息

College of Chemistry and Chemical Engineering, Xinyang Normal University, Xinyang, 464000, China.

出版信息

Mikrochim Acta. 2022 May 10;189(6):217. doi: 10.1007/s00604-022-05309-2.

Abstract

An ultrasensitive fluorescence assay strategy on the basis of carbon dots (CDs) and cDNA-modified gold nanoparticles (AuNP-cDNA) was developed for the determination of microRNA-21 (miRNA-21) via internal filtering effect (IFE). Positively charged CDs (PEI-CDs), the fluorophores in IFE, were synthesized via a hydrothermal method using polyethyleneimine (PEI) as surface ligand. The maximum emission wavelength is located at 500 nm under the excitation of 410 nm. AuNPs, the absorbers, were modified with single-stranded DNA (cDNA), which is completely complementary to miRNA-21. The fluorescence of PEI-CDs is quenched due to the assembly of PEI-CDs and AuNPs-cDNA. In the presence of miRNA-21, the hybridization between miRNA-21 and cDNA causes the release of PEI-CDs and the recovery of fluorescence intensity.The fluorescence recovery degree is linearly correlated with the logarithm of miRNA-21 concentration in the range of 1-1000 fM. This method can be applied to determine miRNA-21 in real serum samples, and the detection results are in well agreement with those of qRT-PCR. The determination of miRNA-21 spiked into diluted human serum samples displays satisfactory recovery within the range 88.44-112.7%, which confirmed the reliability for miRNAs detection in real samples.

摘要

基于碳点 (CDs) 和 cDNA 修饰的金纳米粒子 (AuNP-cDNA) 的超灵敏荧光分析策略,通过内滤效应 (IFE) 用于测定 microRNA-21 (miRNA-21)。正电荷 CDs (PEI-CDs),IFE 中的荧光团,通过水热法使用聚乙烯亚胺 (PEI) 作为表面配体合成。在 410nm 激发下,最大发射波长位于 500nm 处。AuNPs 被修饰为单链 DNA (cDNA),其完全与 miRNA-21 互补。由于 PEI-CDs 和 AuNPs-cDNA 的组装,PEI-CDs 的荧光被猝灭。在 miRNA-21 的存在下,miRNA-21 与 cDNA 之间的杂交导致 PEI-CDs 的释放和荧光强度的恢复。荧光恢复程度与 miRNA-21 浓度的对数在 1-1000 fM 范围内呈线性相关。该方法可用于测定真实血清样品中的 miRNA-21,检测结果与 qRT-PCR 吻合良好。在稀释的人血清样品中添加 miRNA-21 的测定显示出 88.44-112.7%的范围内令人满意的回收率,这证实了在真实样品中检测 miRNAs 的可靠性。

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