State Key Laboratory of Heavy Oil Processing and Center for Bioengineering and Biotechnology, China University of Petroleum (East China), Qingdao, 266580, Shandong, People's Republic of China.
The Affiliated Hospital of Qingdao University, Qingdao, 266003, Shandong, People's Republic of China.
Mikrochim Acta. 2020 May 27;187(6):349. doi: 10.1007/s00604-020-04321-8.
A peptide (Li5-025)-modified gold nanoparticle (AuNP)/(titania (TiO) + 5,10,15,20-tetrakis(4-aminophenyl)-21H,23H-porphine (TAPP))/glassy carbon electrode (GCE) was developed for lipopolysaccharide (LPS) determination. This electrode not only performs well in the electrochemical impedance determination of LPS in serum but can also be easily regenerated under light irradiation. Using Fe(CN) as a redox probe, LPS recognition can be indicated by the significantly increased electron-transfer resistance (R) as a result of the coaction of the increased steric hindrance from the peptide-LPS complex and the electrostatic repulsion between LPS and Fe(CN). The impedimetric signal was acquired in the frequency range 0.1 Hz ~ 100 kHz with an initial voltage of 174 mV and an amplitude of 10 mV. The resistance changes (ΔR) are linearly related to the LPS concentrations in a broad range (0.1 pg mL ~ 100 ng mL) with a low detection limit (0.08 pg mL). Importantly, the electrode shows high selectivity to LPS from Escherichia coli O55:B5 compared to other bacterial sources and considerable anti-interference to 0.1% fetal calf serum, demonstrating its potential application in clinically relevant samples. Another highlight is that the AuNP/(TiO + TAPP)/GCE surface can be photocatalytically regenerated under light irradiation (50 mW cm, 300-2500 nm) without any obvious damage to the electrode microstructure. After simple peptide re-immobilization, the regenerated electrode demonstrates LPS response similar to the peptide less one, and the deviation is only 2.89% after 5-cycle reuse. Graphical abstract A peptide (Li5-025)-modified AuNP/(TiO + TAPP porphine)/GCE was proposed, which not only has excellent electrochemical analytical performances for LPS assay in serum but also can be reused after light irradiation and subsequent peptide re-immobilization.
一种肽(Li5-025)修饰的金纳米粒子(AuNP)/(二氧化钛(TiO)+5,10,15,20-四(4-氨基苯基)-21H,23H-卟啉(TAPP))/玻碳电极(GCE)被开发用于测定脂多糖(LPS)。该电极不仅在血清中 LPS 的电化学阻抗测定中表现出色,而且在光照射下也可以轻松再生。使用 Fe(CN)作为氧化还原探针,由于肽-LPS 复合物的增加的空间位阻和 LPS 与 Fe(CN)之间的静电排斥的共同作用,LPS 识别可以通过电子转移电阻(R)的显著增加来指示。在 0.1 Hz100 kHz 的频率范围内,初始电压为 174 mV,幅度为 10 mV,获得阻抗信号。电阻变化(ΔR)与宽浓度范围内(0.1 pg mL100 ng mL)的 LPS 浓度呈线性关系,检测限低(0.08 pg mL)。重要的是,与其他细菌来源相比,该电极对大肠杆菌 O55:B5 的 LPS 表现出高选择性,对 0.1%胎牛血清具有相当大的抗干扰性,表明其在临床相关样本中的潜在应用。另一个亮点是,AuNP/(TiO+TAPP)/GCE 表面在光照下(50 mW cm,300-2500 nm)可以进行光催化再生,而对电极微结构没有任何明显的损坏。简单地进行肽再固定后,再生电极表现出与未修饰肽相似的 LPS 响应,在 5 次循环重复使用后偏差仅为 2.89%。