Department of Chemistry, Capital Normal University , Beijing, 100048, China.
College of Chemistry and Environmental Engineering, Shandong University of Science and Technology , Qingdao, Shandong 266510, China.
Anal Chem. 2017 Dec 5;89(23):12850-12856. doi: 10.1021/acs.analchem.7b03391. Epub 2017 Nov 17.
Herein, we present a novel gold nanoparticle (AuNP) enumeration-based colorimetric aptamer biosensor for ultrasensitive detection of nucleic acid. This AuNP enumeration-based colorimetric method takes advantages of the distinctive and strong localized surface plasmon resonance light scattering with the dark-field microscope. In our model system, first, cost-effective DNA1 instead of expensive 2-thioethyl ether acetic acid was capped on the surface of AuNPs to form a dense DNA1 layer. Then, two DNA strands (DNA2 and DNA3) in two different solutions were separately asymmetrically functionalized on the AuNPs capped dense DNA1 layer. The subsequent binding of the target DNA could trigger the formation of perfect complementary DNA with a Y shape and adjust the distance between nanoparticles to form AuNP dimers, accompanied by a color change from green to yellow as observed, and thereby modulated the performance of the sensor, which resulted in the ultrahigh sensitivity. With this design, a 43 aM limit of detection was obtained, which exhibited an increase of at least 5-9 orders of magnitude in sensitivity over other colorimetric sensors fabricated using conventional strategies.
在此,我们提出了一种基于金纳米粒子(AuNP)计数的新型比色适体生物传感器,用于超灵敏检测核酸。这种基于 AuNP 计数的比色方法利用了独特且强的局域表面等离子体共振光散射与暗场显微镜。在我们的模型系统中,首先,使用具有成本效益的 DNA1 代替昂贵的 2-硫乙醚乙酸来覆盖 AuNPs 表面,形成致密的 DNA1 层。然后,两条 DNA 链(DNA2 和 DNA3)分别在两种不同的溶液中不对称地功能化在覆盖致密 DNA1 层的 AuNPs 上。随后,目标 DNA 的结合可以触发具有 Y 形的完美互补 DNA 的形成,并调整纳米颗粒之间的距离以形成 AuNP 二聚体,同时观察到颜色从绿色变为黄色,从而调节传感器的性能,从而实现超高灵敏度。通过这种设计,获得了 43 aM 的检测限,与使用传统策略制备的其他比色传感器相比,灵敏度提高了至少 5-9 个数量级。