Institute of Materials Research and Engineering, Agency for Science, Technology, and Research, Singapore 117602, Singapore.
Nucleic Acid Ther. 2013 Aug;23(4):273-80. doi: 10.1089/nat.2013.0421.
Gold nanorods (AuNRs) were used as spectroscopic sensing elements to detect specific DNA sequences with a single-base mismatch sensitivity. The assay was based on the observation that the stabilizing repulsive forces between CTA(+)-coated AuNRs can be removed by citrate ions, which causes aggregation among AuNRs; whereas nucleic acids of different structures[ i.e., peptide nucleic acid (PNA), single-stranded DNA (ssDNA), PNA-DNA complex, and double-stranded DNA (dsDNA)] can retard the aggregation. Moreover, the dsDNA PNA-DNA duplexes provide larger retardation than that by unhybridized ssDNA and PNA probe. This assay can differentiate single-base mismatched targets with base substitution at different locations (center and end) with AuNRs of a larger aspect ratio. Besides ultraviolet-visable spectroscopy measurement of particle assembly-induced plasmonic coupling that in turn provides a spectroscopic detection of the specific DNA, dynamic light scattering and transmission electron microscope (TEM) were used to measure smaller degree of aggregation that can reveal sodium citrate- and dsDNA-AuNRs interactions in fine detail.
金纳米棒(AuNRs)被用作光谱传感元件,以具有单碱基错配灵敏度的方式检测特定的 DNA 序列。该测定基于以下观察结果:CTA(+)包覆的 AuNRs 之间的稳定排斥力可以被柠檬酸根离子去除,这导致 AuNRs 聚集;而不同结构的核酸[即肽核酸(PNA)、单链 DNA(ssDNA)、PNA-DNA 复合物和双链 DNA(dsDNA)]可以阻止聚集。此外,dsDNA PNA-DNA 双链体比未杂交的 ssDNA 和 PNA 探针提供更大的延迟。该测定可以使用更大纵横比的 AuNRs 区分具有不同位置(中心和末端)碱基取代的单碱基错配靶标。除了通过颗粒组装诱导的等离子体耦合的紫外可见光谱测量,这反过来提供了对特定 DNA 的光谱检测之外,还使用动态光散射和透射电子显微镜(TEM)来测量更小程度的聚集,这可以更详细地揭示柠檬酸钠和 dsDNA-AuNRs 相互作用。