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Hybridization chain reaction and DNAzyme-based dual signal amplification strategy for sensitive colorimetric sensing of acetylcholinesterase activity and inhibitor screening in rat blood

机译:杂交链反应和基于DNAzyme的双信号放大策略用于大鼠血液中乙酰胆碱酯酶活性的敏感比色传感和抑制剂筛选

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摘要

We have constructed a novel colorimetric sensing platform for quantitative detection of acetylcholinesterase (AChE) activity and its inhibitor (donepezil) in rat blood, which integrates the signal amplification of DNAzyme and hybridization chain reaction (HCR) with the assembly of gold nanoparticles (AuNPs). Herein, in the presence of AChE and its substrate acetylthiocholine (ATCh), the sensing system exhibits a dramatic decrease in absorbance at 522 nm, where AChE hydrolyzes ATCh into thiocholine, the resulting thiols capture Cu2+from DNAzyme, and then the substrate strand of DNAzyme acts as an initiator to trigger HCR process. The HCR products can induce the assembly of AuNPs via DNA hybridization, accompanying by a sharp color-change from red to blue. When donepezil is added, the enzymatic activity of AChE is suppressed, resulting in an increase in the absorbance at 522 nm. Under optimal conditions, the colorimetric sensing platform shows sensitive responses to AChE and donepezil in the range of 0.02–1.5 mU mL−1and 0.5–100 nM, respectively. The detection limits of AChE and donepezil are as low as 5 μU mL−1and 0.5 nM, respectively. Owing to high sensitivity of the proposed method, various nonspecific interactions can be eliminated with a sufficient dilution, indicating that our strategy has great potential for practical application in neurobiology and pharmacology fields.
机译:我们构建了一种新型比色传感平台,用于定量检测大鼠血液中的乙酰胆碱酯酶(AChE)活性及其抑制剂(多奈哌齐),该平台将DNAzyme和杂交链反应(HCR)的信号放大与金纳米颗粒(AuNPs)组装在一起。在此,在存在AChE及其底物乙酰硫胆碱(ATCh)的情况下,传感系统在522 nm处的吸光度显着降低,其中AChE将ATCh水解为硫代胆碱,所得的硫醇从DNAzyme捕获Cu2 +,然后从底物链DNAzyme充当引发HCR过程的引发剂。 HCR产品可以通过DNA杂交诱导AuNP组装,并伴随着从红色到蓝色的急剧颜色变化。加入多奈哌齐后,AChE的酶活性受到抑制,导致522 nm处的吸光度增加。在最佳条件下,比色传感平台显示出对AChE和多奈哌齐的敏感响应,分别在0.02–1.5 mU mL-1和0.5–100 nM范围内。 AChE和多奈哌齐的检出限分别低至5μUUmLmL-1和0.5μnM。由于该方法的高灵敏度,可以通过充分稀释消除各种非特异性相互作用,这表明我们的策略在神经生物学和药理学领域具有实际应用的巨大潜力。

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