Department of Chemistry, University of California-Irvine, Irvine, California 92697, USA.
Biointerphases. 2008 Sep;3(3):FD23-9. doi: 10.1116/1.2994689.
An ex situ nanoparticle DNA detection assay utilizing DNA-modified nanoparticles attached to DNA monolayer gratings on glass substrates is developed. The assay utilizes the simultaneous hybridization of a single stranded DNA (ssDNA) target molecule to both an amine-modified DNA oligonucleotide attached to an amine-reactive glass surface and a thiol-modified DNA oligonucleotide attached to a 13 nm gold nanoparticle. Surface plasmon resonance imaging measurements are used to characterize the two sequential hybridization adsorption processes employed in the assay, and fluorescence microscopy is used to characterize the formation of DNA monolayer gratings via the photopatterning of the amine-reactive glass slides. First order diffraction measurements utilizing incoherent collimated white light source and a 10 nm bandpass filter centered at 600 nm provided quantitative measurements of target ssDNA down to a concentration of 10 pM. Fourth order diffraction measurements employing a HeNe laser and avalanche photodiode were used to detect target ssDNA adsorption from 10 microl of a solution with a concentration as low as 10 fM, corresponding to 60,000 target DNA molecules. This simple yet sensitive grating-based nanoparticle DNA detection assay should be directly applicable for genetic screening, mRNA expression assays, and microRNA profiling.
开发了一种利用附着在玻璃基底上的 DNA 单层光栅上的 DNA 修饰纳米粒子的体外纳米粒子 DNA 检测分析方法。该分析方法利用单链 DNA (ssDNA) 靶分子同时与附着在胺反应性玻璃表面上的胺修饰 DNA 寡核苷酸和附着在 13nm 金纳米粒子上的巯基修饰 DNA 寡核苷酸杂交。表面等离子体共振成像测量用于表征分析中使用的两个顺序杂交吸附过程,荧光显微镜用于通过胺反应性玻片的光图案化来表征 DNA 单层光栅的形成。利用非相干准直白光光源和中心波长为 600nm 的 10nm 带通滤波器进行的一阶衍射测量提供了定量测量低至 10pM 浓度的靶 ssDNA 的方法。利用氦氖激光器和雪崩光电二极管进行的四阶衍射测量可用于从浓度低至 10fM(对应于 60000 个靶 DNA 分子)的 10 微升溶液中检测靶 ssDNA 的吸附。这种简单而灵敏的基于光栅的纳米粒子 DNA 检测分析方法应该可以直接应用于基因筛选、mRNA 表达分析和 microRNA 分析。