Interfacial Engineering of Hybrid Polydopamine/Polypyrrole Nanosheets with Narrow Band Gaps for Fluorescence Sensing of MicroRNA

材料科学 聚吡咯 生物传感器 石墨烯 荧光 电子转移 纳米技术 聚合 猝灭(荧光) 检出限 光诱导电子转移 聚合物 组合化学 光化学 化学 物理 色谱法 量子力学 复合材料
作者
Mengnan Yang,Zhenqiang Wang,Tao Ding,Jia Tang,Xiyue Xie,Yuxin Xing,Lu Wang,Jixi Zhang,Kaiyong Cai
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:13 (35): 42183-42194 被引量:21
标识
DOI:10.1021/acsami.1c11301
摘要

Nanoquencher-based biosensors have emerged as powerful tools for the detection of tumor markers, where challenges in efficiently docking the π-electron interaction interface toward nucleic acid probes containing π-electron-rich units of bases and fluorescent dyes still remain. Herein, we present hybrid polydopamine/polypyrrole nanosheets (PDA-PPy-NS) with π electron coupling and ultranarrow band gap (0.29 eV) by interfacial engineering of polymer hybrids at the nanoscale. PDA-PPy-NS were first prepared through oxidant-induced polymerization of pyrrole on PDA nanosheets. By utilizing fluorescent-dye-labeled single-stranded DNA as a probe, the hybrid nanoquencher showed ultrahigh fluorescence quenching ability, i.e., a Cy5-ssDNA/nanoquencher mass ratio of 36.9 under the complete quenching condition, which is comparable to that of graphene oxide. It was demonstrated that the energy level coupling of nanosheets and nucleic acid dye (Cy5) was the key factor contributing to the efficient photoinduced electron transfer (PET). Subsequently, the nanoquencher/DNA probe was proved to possess superior sensitivity and selectivity for efficient and reliable detection of miRNA-21 with a detection limit of 23.1 pM. Our work proves that the π-electron-rich biosensor interface can significantly enhance the PET efficiency, providing a theoretical basis for developing novel high-performance sensors.
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