Département de Pharmacochimie Moléculaire, UMR 5063, Grenoble Alpes University - CNRS, France; Département de Biochimie, Toxicologie et Pharmacologie, CHU de Grenoble Site Nord - Institut de Biologie et de Pathologie, F-38041, Grenoble, France.
Département de Pharmacochimie Moléculaire, UMR 5063, Grenoble Alpes University - CNRS, France.
Anal Chim Acta. 2023 Feb 22;1243:340840. doi: 10.1016/j.aca.2023.340840. Epub 2023 Jan 13.
Herein, we report a novel approach for the design of a colorimetric aptasensor, relying on a Dye Salt Aggregation-based Colorimetric Oligonucleotide assay (DYSACO assay). This method is based on the use of an intercalating agent, Nile Blue (NB), whose aggregation capacities (and thus modification of its absorption spectrum) are drastically amplified by adding salts to the working solution. The presence of an aptamer could protect NB from such aggregation process due to its intercalation into double-stranded DNA and/or interaction with nucleobases. In response to the addition of the specific ligand, the competition between NB and the target for binding to the aptamer occurs, resulting in an increase in the dye salt aggregation and then in the blue-to-blank color change of the solution. The proof-of-principle was demonstrated by employing the anti-l-tyrosinamide aptamer and the assay was successfully applied to the trace enantiomer detection, allowing the detection of an enantiomeric impurity down to approximately 2% in a non-racemic sample. Through a reversed mechanism based on the increased capture of NB by DNA upon analyte binding, the sensing platform was further demonstrated for the Hg(II) detection. Water samples of different origin were spiked with Hg(II) analyte at final range concentrations comprised between (0.5-15 μM). An excellent overall recovery of 122 ± 14%; 105 ± 14%; 99 ± 9%; was respectively obtained from river, tap and mineral water, suggesting that the sensor can be used under real sample conditions. The assay was also shown to work for sensing the ochratoxin A and d-arginine vasopressin compounds, revealing its simplicity and generalizability potentialities.
在此,我们报告了一种设计比色适体传感器的新方法,该方法依赖于基于染料盐聚集的比色寡核苷酸测定法(DYSACO 测定法)。该方法基于使用嵌入剂尼罗蓝(NB),其聚集能力(以及因此其吸收光谱的修饰)通过向工作溶液中添加盐而大大增强。由于适体的嵌入双链 DNA 中和/或与碱基相互作用,存在适体可以保护 NB 免受这种聚集过程的影响。响应于添加特定配体,NB 与靶标之间发生与适体结合的竞争,导致染料盐聚集增加,然后溶液颜色从蓝色变为空白。通过使用抗 l-邻苯二胺甲酰胺适体证明了原理验证,并且该测定法成功地应用于痕量对映体检测,允许在非对映体样品中检测到约 2%的对映体杂质。通过基于分析物结合后 DNA 对 NB 的捕获增加的反向机制,该传感平台进一步用于 Hg(II)检测。不同来源的水样以最终浓度范围(0.5-15 μM)加入 Hg(II)分析物。从河水、自来水和矿泉水分别获得了 122 ± 14%;105 ± 14%;99 ± 9%的出色总体回收率,表明该传感器可以在实际样品条件下使用。该测定法还被证明可用于检测赭曲霉毒素 A 和 d-精氨酸加压素化合物,显示出其简单性和通用性潜力。