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Using optical tweezers, single molecule fluorescence and the ZIF268 protein-DNA system to probe mechanotransduction mechanisms

机译:使用光学镊子,单分子荧光和ZIF268蛋白质-DNa系统来探测机械转导机制

摘要

Optical tweezers instruments use laser radiation pressure to trap microscopic dielectric beads. With the appropriate chemistry, such a bead can be attached to a single molecule as a handle, permitting the application of force on the single molecule. Measuring the force applied in real-time is dependent on detecting the bead's displacement from the trapping laser beam axis. Back-focal-plane detection provides a way of measuring the displacement, in two-dimensions, at nanometer or better resolution. The first part of this work will describe the design of a simple and inexpensive position sensing module customized for optical tweezers applications. Single molecule fluorescence is another powerful technique used to obtain microscopic details in biological systems. This technique can detect the arrival of a single molecule into a small volume of space or detect the conformational changes of a single molecule. Combining optical tweezers with single-molecule fluorescence so that one can apply forces on a single molecule while monitoring its effects via single molecule fluorescence provides an even more powerful experimental platform to perform such microscopic studies. Due to the enhanced photobleaching of fluorophores caused by the trapping laser, this combined technology has only been demonstrated under optimized conditions.
机译:光学镊子仪器使用激光辐射压力来捕获微观介电珠。通过适当的化学反应,这种珠子可以附着在单个分子上作为手柄,从而允许在单个分子上施加力。实时测量施加的力取决于检测磁珠从捕获激光束轴的位移。后焦平面检测提供了一种以纳米或更高分辨率测量二维位移的方法。这项工作的第一部分将描述为光镊应用定制的简单且廉价的位置传感模块的设计。单分子荧光是用于获得生物系统微观细节的另一种强大技术。该技术可以检测单个分子进入小空间或检测单个分子的构象变化。将光镊与单分子荧光相结合,以便人们可以在单个分子上施加力,同时通过单分子荧光监控其效果,为进行此类微观研究提供了更为强大的实验平台。由于由捕获激光引起的荧光团增强的光致漂白,这种结合的技术仅在最佳条件下得到证明。

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