State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Laboratory of Advanced Materials, Fudan University, Shanghai 200433, China.
Langmuir. 2013 May 21;29(20):6147-55. doi: 10.1021/la4006828. Epub 2013 May 9.
A new approach for sensitive detection of a specific ssDNA (single-stranded DNA) sequence based on the surface enhanced Raman spectroscopy (SERS) liquid chip is demonstrated. In this method, the probe DNA (targeting to one part of target ssDNA) was attached to the nano-SERS-tags (poly(styrene-co-acrylic acid)/(silver nanoparticles)/silica composite nanospheres), and the capture DNA (targeting to the other part of target ssDNA) was attached to the Fe3O4/poly(acrylic acid) core/shell nanospheres. The nano-SERS-tags with probe DNA were first allowed to undergo hybridization with the target ssDNA in solution to achieve the best efficiency. Subsequently, the magnetic composite nanospheres with capture DNA were added as the capturing substrates of the target ssDNA combined with the nano-SERS-tags. Upon attraction with an external magnet, the nanospheres (including the nano-SERS-tags) were deposited together due to the hybridization, and the deposit sediment was then analyzed by SERS. Quantitative detection of target ssDNA was achieved based on the well-defined linear correlation between the SERS signal intensity and the target ssDNA quantity in the range of 10 nM to 10 pM, and the limit of detection was approximately 10 pM. Multiplexed detection of up to three different ssDNA targets in one sample was demonstrated using three different types of nano-SERS-tags under a single excitation laser. The experimental results indicated that the liquid-phase DNA sequencing method, thus named the SERS liquid chip (SLC) method, holds significant promises for specific detection of trace targets of organisms.
基于表面增强拉曼光谱(SERS)液体芯片,展示了一种用于灵敏检测特定单链 DNA(ssDNA)序列的新方法。在该方法中,探针 DNA(靶向目标 ssDNA 的一部分)连接到纳米 SERS 标签(聚(苯乙烯-co-丙烯酸)/(银纳米粒子)/硅复合纳米球)上,而捕获 DNA(靶向目标 ssDNA 的另一部分)连接到 Fe3O4/聚(丙烯酸)核/壳纳米球上。首先,让带有探针 DNA 的纳米 SERS 标签在溶液中与目标 ssDNA 进行杂交,以达到最佳效率。随后,加入带有捕获 DNA 的磁性复合纳米球作为与纳米 SERS 标签结合的目标 ssDNA 的捕获底物。在外加磁场的吸引下,由于杂交,纳米球(包括纳米 SERS 标签)一起沉积,然后通过 SERS 分析沉积沉淀物。基于 SERS 信号强度与 10 nM 至 10 pM 范围内目标 ssDNA 量之间的良好线性关系,实现了目标 ssDNA 的定量检测,检测限约为 10 pM。使用三种不同类型的纳米 SERS 标签,在单个激发激光下,在一个样品中演示了多达三种不同 ssDNA 靶标的多重检测。实验结果表明,该液相 DNA 测序方法,即 SERS 液体芯片(SLC)方法,有望用于特定检测痕量生物目标物。