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Single-Molecule Enzymology Based On The Principle Of The Millikan Oil Drop Experiment

机译:基于密立根油滴实验原理的单分子酶学

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摘要

The ability to monitor the progress of single molecule enzyme reactions is often limited by the need to use fluorogenic substrates. A method based on the principle of the Millikan Oil Drop Experiment was developed to monitor the change in charge of substrates bound to a nanoparticle and offers a means of detecting single enzyme reactions without fluorescence detection. As a proof of principle of the ability to monitor reactions which result in a change in substrate charge, polymerization on a single DNA template was detected. A custom oligonucleotide was synthesized which allowed for the attachment of single DNA templates to gold nanoparticles with a single polymer tether. The nanoparticles were then tethered to the surface of a microfluidic channel where the positions of the nanoparticles, subjected to an oscillating electric field, were monitored using darkfield microscopy. With short averaging times, the signal-to-noise level was low enough to discriminate changes in charge of less than 1.2%. Polymerization of a long DNA template demonstrated the ability to use the system to monitor single molecule enzymatic activity. Finally, nanoparticle surfaces were modified with thiolated moieties in order to reduce and/or shield the number of unproductive charges and allow for improved sensitivity.
机译:监测单分子酶反应进程的能力通常受使用荧光底物的限制。开发了一种基于密立根油滴实验原理的方法,用于监测与纳米颗粒结合的底物电荷的变化,并提供了无需荧光检测即可检测单个酶反应的方法。作为监测导致底物电荷变化的反应的能力原理的证明,检测到单个DNA模板上的聚合。合成了定制的寡核苷酸,该寡核苷酸允许使用单个聚合物链将单个DNA模板附着到金纳米颗粒上。然后将纳米颗粒束缚到微流体通道的表面,在该表面上,使用暗场显微镜监测纳米颗粒经受振荡电场的位置。平均时间短时,信噪比水平很低,足以区分小于1.2%的电荷变化。长DNA模板的聚合显示了使用该系统监控单分子酶活性的能力。最后,用硫醇化部分修饰纳米颗粒表面,以减少和/或屏蔽非生产性电荷的数量并提高灵敏度。

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