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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Discrimination of the false-positive signals of molecular beacons by combination of heat inactivation and using single walled carbon nanotubes
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Discrimination of the false-positive signals of molecular beacons by combination of heat inactivation and using single walled carbon nanotubes

机译:通过热灭活和使用单壁碳纳米管来区分分子信标的假阳性信号

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摘要

Molecular beacons (MBs) have been extensively used for real-time monitoring of RNA/DNA and protein molecules. However, such versatility also brings about multiple sources of positive signals. Moreover, the covalently attached quencher or fluorophore may even be cleaved from the strand by the exonucleases, followed by complete degradation of the probe. These undesirable false-positive signals (FPSs) have seriously limited the application of MBs to detect real world samples. In this paper, we propose a novel and efficient approach for discrimination of FPSs of MBs due to non-specific MB-protein interactions and nuclease degradation by combination of heat inactivation and using single walled carbon nanotubes (SWNTs). The mechanisms of different DNA-protein interactions that are responsible for the generation of FPSs of MBs were investigated in detail. The proposed strategy can quickly identify the possible sources of FPSs caused by mechanisms other than hybridization in detecting real samples, which would be very helpful in choosing a proper way to modify the structure of the MBs or using a specific inhibitor. The established method was successfully applied to verify the FPSs in the measurement of a plant tissue sample.
机译:分子信标(MBs)已被广泛用于RNA / DNA和蛋白质分子的实时监控。但是,这种多功能性也带来了积极信号的多种来源。而且,共价连接的猝灭剂或荧光团甚至可以被核酸外切酶从链上切割下来,然后探针完全降解。这些不良假阳性信号(FPS)严重限制了MB在检测现实世界样本中的应用。在本文中,我们提出了一种新颖而有效的方法,用于通过结合热灭活和使用单壁碳纳米管(SWNTs)来区分由于非特异性MB蛋白相互作用和核酸酶降解引起的MB FPS。详细研究了导致MBs FPS产生的不同DNA-蛋白质相互作用的机制。所提出的策略可以快速识别由FPS而不是杂交引起的检测实际样品的机制所引起的可能来源,这对于选择适当的方法来修饰MBs的结构或使用特定的抑制剂非常有帮助。所建立的方法已成功地应用于验证植物组织样品测量中的FPS。

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