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首页> 外文期刊>Analytical and bioanalytical chemistry >Aptamer-mediated colorimetric and electrochemical detection of Pseudomonas aeruginosa utilizing peroxidase-mimic activity of gold NanoZyme
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Aptamer-mediated colorimetric and electrochemical detection of Pseudomonas aeruginosa utilizing peroxidase-mimic activity of gold NanoZyme

机译:适体介导的色素和电化学检测假单胞菌铜绿假单胞菌利用金纳比二沸酶的过氧化物酶 - 模拟活性

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摘要

Despite of various advancements in biosensing, a rapid, accurate, and on-site detection of a bacterial pathogen is a real challenge due to the lack of appropriate diagnostic platforms. To address this unmet need, we herein report an aptamer-mediated tunable NanoZyme sensor for the detection of Pseudomonas aeruginosa, an infectious bacterial pathogen. Our approach exploits the inherent peroxidase-like NanoZyme activity of gold nanoparticles (GNPs) in combination with high affinity and specificity of a Pseudomonas aeruginosa-specific aptamer (F23). The presence of aptamer inhibits the inherent peroxidase-like activity of GNPs by simple adsorption on to the surface of GNPs. However, in the presence of cognate target (P. aeruginosa), owing to the high affinity for P. aeruginosa, the aptamer leaves the GNP surface, allowing GNPs to resume their peroxidase-like activity, resulting in oxidation of 3,3,5,5-tetramethylbenzidine (TMB). As TMB is an electrochemically active species, we have been able to translate the NanoZyme-based method into an ultrasensitive electrochemical assay using disposable carbon screen-printed electrode. This approach is highly sensitive and allows us to rapidly detect P. aeruginosa with a low-end detection limit of 60CFU/mL in water within 10min. This generic aptamer-NanoZyme-based electrochemical sensing strategy may, in principle, be applicable for the detection of various other bacterial pathogens.
机译:尽管在生物传感的各种进步,但由于缺乏适当的诊断平台,即可对细菌病原体的快速,准确和现场检测是一个真正的挑战。为了解决这种未满足的需求,我们在本文中报告了一种用于检测假单胞菌铜绿假单胞菌的适体介导的可调谐纳米酶传感器,一种感染性细菌病原体。我们的方法利用金纳米颗粒(GNP)的固有过氧化物酶样纳佐活性与铜绿假单胞菌特异性适体(F23)的高亲和力和特异性组合。 Aptamer的存在通过简单吸附于GNPS的表面上抑制GNP的固有过氧化物酶样活性。然而,在同源靶(P. Aerginosa)的存在下,由于对铜绿假单胞菌的高亲和力,适体留下了GNP表面,使GNP恢复其过氧化物酶样活性,导致氧化3,3,5 ,5-四甲基苯胺(TMB)。由于TMB是一种电化学活性物质,我们能够使用一次性碳丝网印刷电极将基于纳佐的方法转化为超敏电化学测定。这种方法具有高度敏感性,并允许我们在10mIn内以60cfu / ml的低端检测极限进行快速检测P. eruginosa。该基于通用适体 - 纳佐的电化学传感策略原则上可以适用于检测各种其他细菌病原体。

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