Zhou Xin, Cao Peng, Zhu Ye, Lu Wuguang, Gu Ning, Mao Chuanbin
State Key Laboratory of Bioelectronics, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China.
Laboratory of Cellular and Molecular Biology, Jiangsu Branch of China Academy of Chinese Medical Sciences, Nanjing 210028, China.
Nat Mater. 2015 Oct;14(10):1058-64. doi: 10.1038/nmat4377. Epub 2015 Aug 17.
The ability to count biomolecules such as cancer-biomarker miRNAs with the naked eye is seemingly impossible in molecular diagnostics. Here, we show an ultrasensitive naked-eye-counting strategy for quantifying miRNAs by employing T7 phage-a bacteria-specific virus nanoparticle-as a surrogate. The phage is genetically engineered to become fluorescent and capable of binding a miRNA-capturing gold nanoparticle (GNP) in a one-to-one manner. Target miRNAs crosslink the resultant phage-GNP couple and miRNA-capturing magnetic microparticles, forming a sandwich complex containing equimolar phage and miRNA. The phage is then released from the complex and developed into one macroscopic fluorescent plaque in a Petri dish by plating it in a host bacterial medium. Counting the plaques by the naked eye enables the quantification of miRNAs with detection limits of ∼3 and ∼5 aM for single-target and two-target miRNAs, respectively. This approach offers ultrasensitive and convenient quantification of disease biomarkers by the naked eye.
在分子诊断中,用肉眼计数生物分子(如癌症生物标志物微小RNA)似乎是不可能的。在此,我们展示了一种超灵敏的肉眼计数策略,通过使用T7噬菌体(一种细菌特异性病毒纳米颗粒)作为替代物来定量微小RNA。对噬菌体进行基因工程改造,使其具有荧光,并能够以一对一的方式结合捕获微小RNA的金纳米颗粒(GNP)。目标微小RNA使所得的噬菌体-GNP偶联物与捕获微小RNA的磁性微粒交联,形成包含等摩尔噬菌体和微小RNA的夹心复合物。然后将噬菌体从复合物中释放出来,并通过将其接种在宿主细菌培养基中,在培养皿中形成一个宏观的荧光噬菌斑。通过肉眼计数噬菌斑能够分别对单靶标和双靶标微小RNA进行定量,检测限分别约为3 aM和5 aM。这种方法提供了一种超灵敏且方便的通过肉眼对疾病生物标志物进行定量的方法。