Department of Chemistry, ‡Institute of Applied Mechanics, and §Center for Emerging Material and Advanced Devices, National Taiwan University , Taipei 106, Taiwan.
ACS Sens. 2018 Jan 26;3(1):174-182. doi: 10.1021/acssensors.7b00823. Epub 2018 Jan 16.
In this work, we report a highly sensitive colorimetric sensing strategy for cancer biomarker diagnosis using gold nanoparticles (AuNPs) labeled with biotinylated poly(adenine) ssDNA sequences and streptavidin-horseradish peroxidase for enzymatic signal enhancement. By adopting this DNA-AuNP nanoconjugate sensing strategy, we were able to eliminate the complicated and costly thiol-binding process typically used to modify AuNP surfaces with ssDNA. In addition, different antibodies can be introduced to the AuNP surfaced via electrostatic interactions to provide highly specific recognition sites for biomolecular sensing. Moreover, multiple, simultaneous tests can be rapidly performed with low sample consumption by incorporating these surface-modified AuNPs into a paper-based analytical device that can be read using just a smartphone. As a result of these innovations, we were able to achieve a detection limit of 10 pg/mL for a prostate specific antigen in a test that could be completed in as little as 15 min. These results suggest that the proposed paper platform possesses the capability for sensitive, high-throughput, and on-site prognosis in resource-limited settings.
在这项工作中,我们报告了一种使用生物素化聚(腺嘌呤)ssDNA 序列标记的金纳米粒子(AuNPs)和链霉亲和素-辣根过氧化物酶进行酶信号增强的用于癌症生物标志物诊断的高灵敏比色传感策略。通过采用这种 DNA-AuNP 纳米共轭传感策略,我们能够消除通常用于用 ssDNA 修饰 AuNP 表面的复杂且昂贵的巯基结合过程。此外,可以通过静电相互作用将不同的抗体引入 AuNP 表面,为生物分子传感提供高度特异性的识别位点。此外,通过将这些表面修饰的 AuNP 整合到仅使用智能手机即可读取的基于纸张的分析设备中,可以快速进行多次同时测试,同时消耗的样品量很少。由于这些创新,我们能够在 15 分钟内完成的测试中实现对前列腺特异性抗原的检测限为 10pg/mL。这些结果表明,所提出的纸张平台具有在资源有限的环境中进行敏感、高通量和现场预后的能力。