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Gold nanoclusters-based chemiluminescence resonance energy transfer method for sensitive and label-free detection of trypsin

机译:基于金纳米团簇的化学发光共振能量转移方法用于胰蛋白酶的灵敏和无标记检测

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摘要

A chemiluminescence resonance energy transfer (CRET) platform was developed for sensitive and label-free detection of protease by using trypsin as a model analyte. In this CRET platform, bis(2,4,6-trichlorophenyl)oxalate-hydrogen peroxide chemiluminescence (CL) reaction was utilized as an energy donor and bovine serum albumin (BSA)-stabilized gold nanoclusters (Au NCs) as an energy acceptor. The BSA-stabilized Au NCs triggered the CRET phenomenon by accepting the energy from TCPO-H2O2 CL reaction, thus producing intense CL. In the presence of trypsin, the protein template of BSA-stabilized Au NCs was digested, which frustrated the energy transfer efficiency between the CL donor and the BSA-stabilized Au NCs, leading to a significant decrease in the CL signal. The decreased CL signal was proportional to the logarithm of trypsin concentration in the range of 0.01-50.0 mu g mL(-1). The detection limit for trypsin was 9 ng mL(-1) and the relative standard deviations were lesser than 3% (n=11). This Au NCs-based CRET platform was successfully applied to the determination of trypsin in human urine samples, demonstrating its potential application in clinical diagnosis. (C) 2015 Elsevier B.V. All rights reserved.
机译:通过使用胰蛋白酶作为模型分析物,开发了一种化学发光共振能量转移(CRET)平台,用于灵敏且无标记的蛋白酶检测。在此CRET平台中,草酸双(2,4,6-三氯苯基)草酸酯-过氧化氢化学发光(CL)反应用作能量供体,牛血清白蛋白(BSA)稳定化的金纳米簇(Au NCs)作为能量受体。 BSA稳定的Au NCs接受TCPO-H2O2 CL反应产生的能量,从而触发了CRET现象,从而产生了强烈的CL。在存在胰蛋白酶的情况下,消化了BSA稳定的Au NCs的蛋白质模板,这破坏了CL供体和BSA稳定的Au NCs之间的能量转移效率,导致CL信号显着降低。降低的CL信号与胰蛋白酶浓度的对数成正比,范围为0.01-50.0μg mL(-1)。胰蛋白酶的检出限为9 ng mL(-1),相对标准偏差小于3%(n = 11)。这个基于Au NCs的CRET平台已成功应用于人尿样品中胰蛋白酶的测定,证明了其在临床诊断中的潜在应用。 (C)2015 Elsevier B.V.保留所有权利。

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