Li Chao, Li Xiaoxi, Wei Luming, Liu Muyun, Chen Yangyang, Li Genxi
State Key Laboratory of Pharmaceutical Biotechnology , Department of Biochemistry , Nanjing University , 210093 , China . Email:
Laboratory of Biosensing Technology , School of Life Sciences , Shanghai University , 200444 , China.
Chem Sci. 2015 Jul 1;6(7):4311-4317. doi: 10.1039/c5sc00891c. Epub 2015 May 5.
Various strategies have been proposed for the detection of disease protein biomarkers; however, most methods are too expensive, cumbersome or limited in sensitivity for clinical use. Here, we report that a fabricated complex can be used as a powerful tool to detect trace proteins in complex samples. In this strategy, a DNA-protein complex that comprises of one target molecule and two or more deoxyribozyme-containing probes can exhibit autonomous cleavage behavior on the surface of the substrate DNA modified electrode. In the meantime, the complex can remove the cleaved DNA fragment from the electrode surface by taking advantage of the proximity effect. The proposed approach allows one-step and highly sensitive detection of a variety of targets based on the changes of the direct electrochemical readout. Moreover, this method may also have considerable advantages over the commonly reported DNA amplification-assisted immunoassays, particularly in terms of assay simplicity and cost, which may hold great potential for application in resource-constrained regions.
已经提出了各种用于检测疾病蛋白质生物标志物的策略;然而,大多数方法对于临床应用来说过于昂贵、繁琐或灵敏度有限。在这里,我们报告一种人工合成的复合物可以用作检测复杂样品中痕量蛋白质的强大工具。在这种策略中,由一个靶分子和两个或更多含脱氧核酶的探针组成的DNA-蛋白质复合物可以在底物DNA修饰电极表面表现出自主切割行为。同时,该复合物可以利用邻近效应从电极表面去除切割后的DNA片段。所提出的方法基于直接电化学读数的变化,能够一步实现对多种靶标的高灵敏度检测。此外,该方法相对于常见报道的DNA扩增辅助免疫测定法可能也具有相当大的优势,特别是在检测简便性和成本方面,这可能在资源有限的地区具有巨大的应用潜力。