Department of Chemistry, Susquehanna University, 514 University Avenue, Selinsgrove, PA 17870, USA.
J Anal Methods Chem. 2012;2012:327603. doi: 10.1155/2012/327603. Epub 2012 Mar 27.
Gold nanoparticles have been used as a probe to detect low (<10 ppb) concentrations of quadruplex DNA. These nanoparticles display a tendency to form aggregates in the presence of certain quadruplex forms, as observed via enhanced plasmon resonance light scattering (PRLS) signals. These nanoparticles showed differing degrees of interactions with different types of quadruplex and mixed sequences but no interaction with duplex DNA. Enhancement of PRLS signals greater than 50% was observed at nanomolar DNA concentration, and a lower limit of detection of 2.1 nM was established for three different quadruplex DNA sequences, including the thrombin-inhibiting single-stranded 15 mer aptamer DNA, d(GGTTGGTGTGGTTGG), and the double-stranded 12 mer DNA, d(G4T4G4). Two different sample preparation protocols were used for the PRLS experiments, and they yielded similar results.
金纳米粒子已被用作探针来检测四链体 DNA 的低浓度 (<10 ppb)。这些纳米粒子在存在某些四链体形式时表现出形成聚集体的趋势,这可以通过增强的等离子体共振光散射 (PRLS) 信号观察到。这些纳米粒子与不同类型的四链体和混合序列表现出不同程度的相互作用,但与双链 DNA 没有相互作用。在纳摩尔 DNA 浓度下观察到 PRLS 信号增强超过 50%,并且为三个不同的四链体 DNA 序列(包括抑制凝血酶的单链 15 mer 适体 DNA、d(GGTTGGTGTGGTTGG)和双链 12 mer DNA、d(G4T4G4))建立了 2.1 nM 的检测下限。PRLS 实验使用了两种不同的样品制备方案,它们产生了相似的结果。