首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >A DNA hybridization detection based on fluorescence resonance energy transfer between dye-doped core-shell silica nanoparticles and gold nanoparticles
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A DNA hybridization detection based on fluorescence resonance energy transfer between dye-doped core-shell silica nanoparticles and gold nanoparticles

机译:基于染料核壳二氧化硅纳米粒子和金纳米粒子之间荧光共振能量转移的DNA杂交检测

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摘要

A novel and efficient method to evaluate the DNA hybridization based on a fluorescence resonance energy transfer (FRET) system, with fluorescein isothiocyanate (FITC)-doped fluorescent silica nanoparticles (SiNPs) as donor and gold nanoparticles (AuNPs) as acceptor, has been reported. The strategy for specific DNA sequence detecting is based on DNA hybridization event, which is detected via excitation of SiNPs-oligonucleotide conjugates and energy transfer to AuNPs-oligonucleotide conjugates. The proximity required for FRET arises when the SiNPs-oligonucleotide conjugates hybridize with partly complementary AuNPs-oligonucleotide conjugates, resulting in the fluorescence quenching of donors, SiNPs-oligonucleotide conjugates, and the formation of a weakly fluorescent complex, SiNPs-dsDNA-AuNPs. Upon the addition of the target DNA sequence to SiNPs-dsDNA-AuNPs complex, the fluorescence restores (turn-on). Based on the restored fluorescence, a homogeneous assay for the target DNA is proposed. Our results have shown that the linear range for target DNA detection is 0-35.0 nM with a detection limit (3σ) of 3.0 picomole. Compared with FITC-dsDNA-AuNPs probe system, the sensitivity of the proposed probe system for target DNA detection is increased by a factor of 3.4-fold.
机译:已经报道了一种新颖有效的方法,用于评估基于荧光共振能量转移(FRET)系统的DNA杂交,其中掺有异硫氰酸荧光素(FITC)的荧光二氧化硅纳米颗粒(SiNPs)作为施主,而金纳米颗粒(AuNPs)作为受主。特定DNA序列检测的策略基于DNA杂交事件,该事件通过SiNPs-寡核苷酸结合物的激发和能量转移到AuNPs-寡核苷酸结合物来检测。当SiNPs-寡核苷酸共轭物与部分互补的AuNPs-寡核苷酸共轭物杂交时,FRET所需的接近性出现,导致供体SiNPs-寡核苷酸共轭物的荧光猝灭,并形成弱荧光复合物SiNPs-dsDNA-AuNPs。在将靶DNA序列添加到SiNPs-dsDNA-AuNPs复合物后,荧光恢复(开启)。基于恢复的荧光,提出了对靶DNA的均相测定。我们的结果表明,目标DNA检测的线性范围是0-35.0 nM,检测限(3σ)为3.0皮摩尔。与FITC-dsDNA-AuNPs探针系统相比,该探针系统对目标DNA的检测灵敏度提高了3.4倍。

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