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Ultrasensitive nuclease activity and inhibition assay using microchip electrophoresis with laser induced fluorescence detection

机译:微芯片电泳和激光诱导荧光检测的超灵敏核酸酶活性和抑制测定

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摘要

novel microchip electrophoresis method with laser induced fluorescence detection (MCE-LIF) was developed for ultrasensitive detection of nuclease activity and inhibitors. S1 nuclease was chosen as the model nuclease to demonstrate the proof-of-concept of the proposed approach. In this assay, the fluorescein-labeled ssDNA (FAM-ssDNA) was used as a signal reporter. In the presence of nuclease, FAM-ssDNA was digested to 5-FAM-nucleoside monophosphates and short oligonucleotide fragments. However, the cleavage reaction of FAM-ssDNA with nuclease was prohibited in the presence of inhibitors. Detection of S1 nuclease activity and inhibitors can be achieved by separating FAM-ssDNA and FAM-5-nucleoside monophosphates, and detecting the fluorescence intensity of FAM-5-nucleoside monophosphates in the MCE-LIF platform. The calibration curve showed a linearity in the range of S1 nuclease concentrations from 0.002 to 0.2 U mL(-1). Based on a signaloise ratio (S/N) of 3, the detection limit was estimated to be 0.001 U mL(-1), which was about 1-3 orders of magnitude more sensitive than those of the developed approaches. The proposed method was low-cost and simple in its operation, and the capabilities for target detection from complex fluids and screening of nuclease inhibitors were verified.
机译:开发了一种新型的激光诱导荧光检测微芯片电泳方法(MCE-LIF),用于核酸酶活性和抑制剂的超灵敏检测。选择S1核酸酶作为模型核酸酶,以证明所提出方法的概念验证。在该测定中,将荧光素标记的ssDNA(FAM-ssDNA)用作信号报告基因。在存在核酸酶的情况下,将FAM-ssDNA消化成5-FAM-核苷单磷酸和短寡核苷酸片段。然而,在抑制剂存在下,FAM-ssDNA与核酸酶的裂解反应被禁止。通过分离FAM-ssDNA和FAM-5-核苷单磷酸,并在MCE-LIF平台上检测FAM-5-核苷单磷酸的荧光强度,可以检测S1核酸酶活性和抑制剂。校正曲线在S1核酸酶浓度范围为0.002至0.2 U mL(-1)范围内显示线性关系。基于3的信噪比(S / N),检测极限估计为0.001 U mL(-1),其灵敏度比已开发方法高1-3个数量级。该方法成本低廉,操作简便,并验证了从复杂流体中进行目标检测和核酸酶抑制剂筛选的能力。

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