State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Science of Guangxi Normal University, Guilin, 541004, China.
Mikrochim Acta. 2018 Jan 16;185(2):119. doi: 10.1007/s00604-018-2673-1.
The authors describe a fluorescence polarization assay for HIV-DNA. It is based on the use of gold nanoparticles (AuNPs) modified with DNA dendritic macromolecules that act as signal amplifiers. In the presence of HIV-DNA, the AuNP-DNA dendritic macromolecules and fluorescently labeled DNA probe combine with HIV-DNA in a sandwich format to form a conjugate. This reaction slows down the rotational speed of the labeled DNA probe because of the increase of molecular weight and volume. This increases fluorescence polarization and the sensitivity of the system. The relative fluorescence polarization values increase linearly in the 150 pM to 6 nM HIV-DNA concentration range, with a 73 pM detection limit. The results show this amplification strategy to be most useful for ultrasensitive determination of oligonucleotides by means of fluorescence polarization. Graphical abstract Schematic of a novel fluorescence polarization assay for the HIV-DNA. Ultrasensitive detection is accomplished by using AuNP-DNA dendritic macromolecules as signal amplification factor.
作者描述了一种用于 HIV-DNA 的荧光偏振测定法。它基于使用金纳米粒子 (AuNP) 修饰 DNA 树枝状大分子,这些大分子作为信号放大器。在 HIV-DNA 的存在下,AuNP-DNA 树枝状大分子和荧光标记的 DNA 探针与 HIV-DNA 以三明治的形式结合形成缀合物。由于分子量和体积的增加,这会减缓标记 DNA 探针的旋转速度。这会增加荧光偏振和系统的灵敏度。相对荧光偏振值在 150 pM 至 6 nM HIV-DNA 浓度范围内呈线性增加,检测限为 73 pM。结果表明,这种扩增策略对于通过荧光偏振法对寡核苷酸进行超灵敏测定非常有用。