Lucarelli Fausto, Marrazza Giovanna, Mascini Marco
Department of Chemistry, University of Florence, via della Lastruccia 3, 50019 Sesto Fiorentino, Florence, Italy.
Langmuir. 2006 Apr 25;22(9):4305-9. doi: 10.1021/la053187m.
This study describes the development and characterization of a novel dendritic-like signal amplification pathway. Such an analytical strategy relies on the use of streptavidin and biotinylated alkaline phosphatase, which can be simply and conveniently self-assembled to build nanoarchitectures rich in enzyme labels. The performance of this enzyme-based amplification route was demonstrated in connection with the electrochemical sensing of DNA sequences. Compared to the commercially available streptavidin-conjugated alkaline phosphatase labels, a single generation of the streptavidin/biotinylated alkaline phosphatase assembly allowed a 15-20-fold enhancement of the electroanalytical signals. The higher sensitivity allowed by the dendritic-like route was attributed to the lower steric hindrance of the proteins employed for this amplification path. As low as 50 pmol/L of a 388-bp-long amplicon identifying Salmonella spp. was easily detected. The experimental results additionally demonstrated that the sensitivity of the method could be further increased in a linear fashion with the number of protein-enzyme generations.
本研究描述了一种新型树状信号放大途径的开发与特性。这种分析策略依赖于链霉亲和素和生物素化碱性磷酸酶的使用,它们可以简单方便地自组装以构建富含酶标记的纳米结构。这种基于酶的放大途径的性能在与DNA序列的电化学传感相关方面得到了证明。与市售的链霉亲和素偶联碱性磷酸酶标记相比,单代链霉亲和素/生物素化碱性磷酸酶组装使电分析信号增强了15至20倍。树状途径所允许的更高灵敏度归因于用于此放大途径的蛋白质的空间位阻较低。低至50 pmol/L的识别沙门氏菌属的388 bp长扩增子很容易被检测到。实验结果还表明,该方法的灵敏度可以随着蛋白质 - 酶代的数量以线性方式进一步提高。