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Investigations of fluorescence resonance energy transfer between CdTe quantum dot donors and gold nanoparticle quenchers in DNA sensing

机译:DNA传感中CdTe量子点供体与金纳米粒子猝灭剂之间的荧光共振能量转移的研究

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We used luminescent CdTe quantum dots (QDs) as energy donors and gold nanoparticles (AuNPs) as accepter in fluorescent resonance energy transfer (FRET) assays. CdTe QDs donors with 2.5 nm in size and AuNPs with 16 nm in size were synthesized, and more than 95% overlap between emission spectrum of the CdTe QDs and the absorption spectrum of AuNPs was confirmed. The synthesized donor and accepter were linked to 5' and 3' end of two designed complementary single-stranded DNA (ssDNA), respectively, sensing system was then composed by hybridizing the ssDNA into a double stranded DNA (dsDNA; i.e. CdTe-dsDNA-Au). The prepared CdTe QDs, AuNPs, and CdTe-dsDNA-Au were characterized by UV-vis spectra, fluorescence spectra, and electrophoresis method. Furthermore, FRET efficiency was estimated to be 74.6% for the FRET-pairs in dsDNA. The complementary single-stranded target-DNA was subjected to this sensing system to measure the fluorescence recovery. The dependence of fluorescence intensity on pH value, time, and amount of added target-DNA was investigated, respectively. The resulting data exhibited that pH 7.0 is optimum for both interaction of CdTe QDs and AuNPs and stability of DNA helix. After 12h of stand, the CdTe-dsDNA-Au sensing system becomes unstable. Fluorescence spectra of the sensing system showed that fluorescence recovery was enhanced with increasing addition of target-DNA in a certain range. Our data showed that an effective biosensing system was constructed base on fluorescent resonance energy transfer.
机译:我们用发光CDTE量子点(QDS)作为能量供体和金纳米颗粒(AUNP),作为荧光共振能量转移(FRET)测定中的Accepter。合成了CdTe QDS供体,尺寸为2.5nm,尺寸为16nm,尺寸为16nm,CdTe QD的发射谱之间的发射光谱与AUNP的吸收光谱之间有超过95%的重叠。合成的供体和accepter分别与两个设计的互补单链DNA(SSDNA)的5'和3'末端连接,然后通过将SSDNA杂交成双链DNA(DSDNA;即CDTE-DSDNA - au)。通过UV-Vis光谱,荧光光谱和电泳方法表征制备的CDTE QDS,AUNP和CDTE-DSDNA-Au。此外,在DSDNA中的FRET对估计FRET效率为74.6%。对该感测系统进行互补的单链靶DNA以测量荧光回收率。研究了荧光强度对pH值,时间和添加的靶DNA的量的依赖性。所得到的数据表明,pH 7.0对于CdTe QD的相互作用和DNA螺旋的稳定性是最佳的。在12小时后,CDTE-DSDNA-AU传感系统变得不稳定。感测系统的荧光光谱显示,随着在一定范围内的增加的靶-DNA增加,增强了荧光回收。我们的数据表明,荧光谐振能量转移构建有效的生物传感系统。

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