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Understanding the competitive interactions in aptamer–gold nanoparticle based colorimetric assays using surface enhanced Raman spectroscopy (SERS)

机译:使用表面增强拉曼光谱(SERS)了解基于适体-金纳米颗粒的比色测定法中的竞争相互作用

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Aptamera€“gold nanoparticle (AuNP) based colorimetric assays have become increasingly popular as viable rapid detection methods, but the molecular interactions governing the mechanism and successful interpretation of color changes have not been explored well. The objective of this study was to evaluate the competitive interactions that occur in this detection assay at the molecular level by employing surface enhanced Raman spectroscopy (SERS). The SERS signals of molecules in close proximity to AuNPs were exploited to give information on AuNP surface coverage as well as ssDNA aptamer conformational changes during target capture. Two antibiotics, ampicillin and kanamycin, and their respective aptamers were used in this study. The results indicate that the reason for the lack of AuNP aggregation with ampicillin could be due to a stronger binding affinity of AuNPs to ampicillin than to the aptamer. Kanamycin, on the other hand, induced AuNP aggregation to produce a color change and the SERS data indicate a stronger binding affinity of kanamycin to the aptamer than to the AuNPs as well as aptamer conformational changes. The use of SERS can be a potential tool to rapidly screen and validate the aptamer and target interaction for the application of aptamera€“gold nanoparticle (AuNP) based colorimetric assays.
机译:Aptamera金纳米颗粒(AuNP)的比色测定法已成为可行的快速检测方法,但控制该机理和成功解释颜色变化的分子相互作用尚未得到很好的探索。这项研究的目的是通过使用表面增强拉曼光谱(SERS)评估在分子水平上此检测分析中发生的竞争性相互作用。利用与AuNPs紧密接近的分子的SERS信号来提供目标捕获过程中AuNP表面覆盖率以及ssDNA适体构象变化的信息。在这项研究中使用了两种抗生素,氨苄青霉素和卡那霉素,以及它们各自的适体。结果表明,氨苄青霉素缺乏AuNP聚集的原因可能是由于AuNP与氨苄青霉素的结合亲和力强于适体。另一方面,卡那霉素诱导AuNP聚集以产生颜色变化,并且SERS数据表明卡那霉素对适体的结合亲和力大于对AuNP以及适体构象变化的结合亲和力。 SERS的使用可能是快速筛选和验证适体和靶相互作用的潜在工具,适用于基于适体,金纳米颗粒(AuNP)的比色测定。

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