Zeng Ruijin, Luo Zhongbin, Zhang Lijia, Tang Dianping
Key Laboratory of Analytical Science for Food Safety and Biology (MOE & Fujian Province), State Key Laboratory of Photocatalysis on Energy and Environment, Department of Chemistry , Fuzhou University , Fuzhou , 350108 , People's Republic of China.
Anal Chem. 2018 Oct 16;90(20):12299-12306. doi: 10.1021/acs.analchem.8b03889. Epub 2018 Sep 28.
Pressure-based bioassays incorporating biomolecular recognition with a catalyzed gas-generation reaction have been developed for gas biosensors, but most involve poor sensitivity and are unsuitable for routine use. Herein we design an innovative gas pressure-based biosensing platform for the detection of Kanamycin (Kana) on polyaniline nanowires-functionalized reduced graphene oxide (PANI/rGO) framework by using platinum nanozyme-catalyzed gas generation. The signal was amplified by coupling with catalytic hairpin assembly (CHA) and strand-displacement amplification (SDA). Upon target Kana introduction, the analyte initially triggered a SDA reaction between hairpin DNA1 and hairpin DNA2, and then induced CHA conjugation between magnetic bead-labeled hairpin DNA3 (MB-H3) and platinum nanoparticle-labeled hairpin DNA4 (Pt-H4) to form a three-dimensional network. Numerous platinum nanoparticles (peroxidase-like nanozymes) were carried over with magnetic beads to reduce hydrogen peroxide into oxygen. The as-produced gas compressed PANI/rGO frameworks (modified to polyurethane sponge, used as the piezoelectric materials) in a homemade pressure-tight device, thus causing the increasing current of PANI/rGO sponge thanks to its deformation. The change in the current caused by the as-generated gas pressure was determined on an electrochemical workstation. Under optimum conditions, PANI/rGO sponge exhibited outstanding compressibility, stable signal-waveform output, fast response and recovery time (≈109 ms), and the current increased with the increasing Kana concentration within a dynamic working range of 0.2-50 pM at a detection limit of 0.063 pM. Good reproducibility, specificity, and acceptable precision were acquired for Kana analysis. In addition, the accuracy of this method was monitored to evaluate real milk samples with the well-matched results obtained by using the referenced Kana ELISA kit.
基于压力的生物测定法将生物分子识别与催化气体生成反应相结合,已被用于气体生物传感器的开发,但大多数灵敏度较低,不适合常规使用。在此,我们设计了一种创新的基于气体压力的生物传感平台,通过使用铂纳米酶催化气体生成,来检测聚苯胺纳米线功能化还原氧化石墨烯(PANI/rGO)框架上的卡那霉素(Kana)。通过与催化发夹组装(CHA)和链置换扩增(SDA)耦合来放大信号。引入目标Kana后,分析物首先触发发夹DNA1和发夹DNA2之间的SDA反应,然后诱导磁珠标记的发夹DNA3(MB-H3)和铂纳米颗粒标记的发夹DNA4(Pt-H4)之间的CHA结合,形成三维网络。大量铂纳米颗粒(类过氧化物酶纳米酶)随磁珠携带,将过氧化氢还原为氧气。产生的气体在自制的压力密封装置中压缩PANI/rGO框架(改性为聚氨酯海绵,用作压电材料),由于其变形,从而导致PANI/rGO海绵的电流增加。在电化学工作站上测定由产生的气体压力引起的电流变化。在最佳条件下,PANI/rGO海绵表现出出色的压缩性、稳定的信号波形输出、快速的响应和恢复时间(≈109 ms),并且在0.2-50 pM的动态工作范围内,电流随Kana浓度的增加而增加,检测限为0.063 pM。Kana分析具有良好的重现性、特异性和可接受的精密度。此外,通过使用参考Kana ELISA试剂盒获得的结果与实际牛奶样品评估的该方法的准确性相匹配。