College of Chemistry and Chemical Engineering, Qingdao Application Technology Innovation Center of Photoelectric Biosensing for Clinical Diagnosis and Treatment, Shandong Sino-Japanese Center for Collaborative Research of Carbon Nanomaterials, Instrumental Analysis Center of Qingdao University, Qingdao University, Qingdao, 266071, China.
College of Chemistry and Chemical Engineering, Qingdao Application Technology Innovation Center of Photoelectric Biosensing for Clinical Diagnosis and Treatment, Shandong Sino-Japanese Center for Collaborative Research of Carbon Nanomaterials, Instrumental Analysis Center of Qingdao University, Qingdao University, Qingdao, 266071, China; School of Rehabilitation Sciences and Engineering, University of Health and Rehabilitation Sciences, Qingdao, 266071, China.
Biosens Bioelectron. 2024 Jul 15;256:116236. doi: 10.1016/j.bios.2024.116236. Epub 2024 Apr 3.
Au nano-clusters (Au NCs) were promising electrochemiluminescence (ECL) nano-materials. However, the small size of Au NCs presented a challenge in terms of their immobilization during the construction of an ECL biosensing platform. This limitation significantly hindered the wider application of Au NCs in the ECL field. In this work, we successfully used the reducibility of TiC to fabricate in situ a self-enhanced nano-probe TiC-TiO-Au NCs. The strategy of in situ generation not only improved the immobilization of Au NCs on the probe but also eliminated the requirement of adding reducing agents during preparation. In addition, in situ generated TiO could serve as a co-reaction accelerator, shortening the electron transfer distance between SO and Au NCs, thereby improving the utilization of intermediates and enhancing the ECL response of Au NCs. The constructed ECL sensing platform could achieve sensitive detection of polynucleotide kinase (PNK). At the same time, the 5'-end phosphate group of DNA phosphorylation could chelate with a large amount of Ti on the surface of TiC, thereby achieving the goal of specific detection of PNK. The sensor based on self-enhanced ECL probes had a broad dynamic range spanning for PNK detection from 10.0 to 1.0 × 10 μU mL, with a limit of detection of 1.6 μU mL. Moreover, the ECL sensor showed satisfactory detection performance in HeLa cell lysate and serum. This study not only provided insights for addressing the issue of ECL luminescence efficiency in Au NCs but also presented novel concepts for ECL self-enhancement strategies.
金纳米簇(Au NCs)是一种很有前途的电致化学发光(ECL)纳米材料。然而,Au NCs 的小尺寸在构建 ECL 生物传感平台时对其固定化提出了挑战。这一限制极大地阻碍了 Au NCs 在 ECL 领域的更广泛应用。在这项工作中,我们成功地利用了 TiC 的还原性原位制备了自增强纳米探针 TiC-TiO-Au NCs。这种原位生成的策略不仅提高了探针上 Au NCs 的固定化程度,而且消除了在制备过程中添加还原剂的要求。此外,原位生成的 TiO 可以作为共反应加速剂,缩短 SO 和 Au NCs 之间的电子转移距离,从而提高中间体的利用率,增强 Au NCs 的 ECL 响应。构建的 ECL 传感平台可以实现对多核苷酸激酶(PNK)的灵敏检测。同时,DNA 磷酸化的 5'-端磷酸基团可以与 TiC 表面的大量 Ti 螯合,从而实现 PNK 的特异性检测。基于自增强 ECL 探针的传感器具有较宽的动态检测范围,可用于检测 10.0 至 1.0×10 μU mL 的 PNK,检测限低至 1.6 μU mL。此外,ECL 传感器在 HeLa 细胞裂解液和血清中表现出令人满意的检测性能。本研究不仅为解决 Au NCs 的 ECL 发光效率问题提供了思路,也为 ECL 自增强策略提供了新的概念。