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金纳米棒聚集的紫外-可见光谱和动态光散射研究。

UV-vis spectroscopy and dynamic light scattering study of gold nanorods aggregation.

机构信息

Institute of Materials Research and Engineering, Agency for Science, Technology, and Research, Singapore 117602, Singapore.

出版信息

Nucleic Acid Ther. 2013 Aug;23(4):273-80. doi: 10.1089/nat.2013.0421.

Abstract

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.

摘要

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。

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