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Electrokinetic trapping at the one nanometer limit

机译:一纳米极限的电动捕获

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Anti-Brownian electrokinetic traps have been used to trap and study the free-solution dynamics of large protein complexes and long chains of DNA. Small molecules in solution have thus far proved too mobile to trap by any means. Here we explore the ultimate limits on trapping single molecules. We developed a feedback-based anti-Brownian electrokinetic trap in which classical thermal noise is compensated to the maximal extent allowed by quantum measurement noise. We trapped single fluorophores with a molecular weight of <1 kDa and a hydrodynamic radius of 6.7 A for longer than one second, in aqueous buffer at room temperature. This achievement represents an 800-fold decrease in the mass of objects trapped in solution, and opens the possibility to trap and manipulate any soluble molecule that can be fluores-cently labeled. To illustrate the use of this trap, we studied the binding of unlabeled RecA to f luorescently labeled single-stranded DNA. Binding of RecA induced changes in the DNA diffusion coefficient, electrophoretic mobility, and brightness, all of which were measured simultaneously and on a molecule-by-molecule basis. This device greatly extends the size range of molecules that can be studied by room temperature feedback trapping, and opens the door to further studies of the binding of unmodified proteins to DNA in free solution.
机译:反布朗电动势阱已用于捕获和研究大蛋白复合物和DNA长链的自由溶液动力学。迄今为止,溶液中的小分子已被证明太易移动而无法以任何方式捕获。在这里,我们探索捕获单个分子的极限。我们开发了一种基于反馈的抗布朗电动势阱,其中经典的热噪声被补偿到了量子测量噪声所允许的最大程度。我们在室温下在水性缓冲液中捕获分子量小于1 kDa且流体动力学半径为6.7 A的单个荧光团超过一秒钟。这一成就代表了溶液中捕获的物体质量减少了800倍,并为捕获和操作任何可被荧光标记的可溶性分子打开了可能性。为了说明此陷阱的用途,我们研究了未标记的RecA与荧光标记的单链DNA的结合。 RecA的结合导致DNA扩散系数,电泳迁移率和亮度的变化,所有这些变化都是同时且逐个分子地进行测量的。该装置大大扩展了可通过室温反馈捕获法研究的分子的大小范围,并为进一步研究未修饰蛋白质与游离溶液中DNA的结合打开了大门。

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