Department of Bioproducts and Biosystems Engineering, University of Minnesota Twin Cities, St. Paul, MN, USA.
USDA Forest Service, Northern Research Station, St. Paul, MN, 55108, USA.
Sci Rep. 2017 Oct 25;7(1):14011. doi: 10.1038/s41598-017-14580-w.
The aggregation of gold nanoparticles (AuNPs) is known to induce an enhancement of localized surface plasmon resonance due to the coupling of plasmonic fields of adjacent nanoparticles. Here we show that AuNPs aggregation also causes a significant enhancement of chemiluminescence in the presence of luminophores. The phenomenon is used to introduce a rapid and sensitive DNA detection method that does not require amplification. DNA probes conjugated to AuNPs were used to detect a DNA target sequence specific to the fungus Ceratocystis fagacearum, causal agent of oak wilt. The hybridization of the DNA target with the DNA probes results in instantaneous aggregation of AuNPs into nanoballs, leading to a significant enhancement of luminol chemiluminescence. The enhancement reveals a linear correlation (R = 0.98) to the target DNA concentration, with a limit of detection down to 260 fM (260 × 10 M), two orders of magnitude higher than the performance obtained with plasmonic colorimetry and absorption spectrometry of single gold nanoparticles. Furthermore, the detection can be performed within 22 min using only a portable luminometer.
金纳米粒子(AuNPs)的聚集已知会由于相邻纳米粒子的等离子体场的耦合而引起局部表面等离子体共振的增强。在这里,我们表明 AuNPs 聚集也会导致在存在发光体的情况下化学发光的显著增强。该现象用于引入一种快速灵敏的 DNA 检测方法,该方法不需要扩增。AuNPs 偶联的 DNA 探针用于检测特定于真菌 Ceratocystis fagacearum 的 DNA 靶序列,该真菌是橡树萎蔫病的病原体。DNA 靶与 DNA 探针的杂交导致 AuNPs 瞬间聚集形成纳米球,从而显著增强了鲁米诺化学发光。增强显示出与靶 DNA 浓度的线性相关性(R = 0.98),检测限低至 260 fM(260×10 M),比等离子体比色法和单金纳米粒子吸收光谱法的性能高两个数量级。此外,仅使用便携式光度计即可在 22 分钟内完成检测。