Backer Adam S, Moerner W E
Opt Express. 2015 Feb 23;23(4):4255-76. doi: 10.1364/OE.23.004255.
Measurements of the orientational freedom with which a single molecule may rotate or 'wobble' about a fixed axis have provided researchers invaluable clues about the underlying behavior of a variety of biological systems. In this paper, we propose a measurement and data analysis procedure based on a widefield fluorescence microscope image for quantitatively distinguishing individual molecules that exhibit varying degrees of rotational mobility. Our proposed technique is especially applicable to cases in which the molecule undergoes rotational motions on a timescale much faster than the framerate of the camera used to record fluorescence images. Unlike currently available methods, sophisticated hardware for modulating the polarization of light illuminating the sample is not required. Additional polarization optics may be inserted in the microscope's imaging pathway to achieve superior measurement precision, but are not essential. We present a theoretical analysis, and benchmark our technique with numerical simulations using typical experimental parameters for single-molecule imaging.
对单个分子围绕固定轴旋转或“摆动”的取向自由度的测量,为研究人员提供了关于各种生物系统潜在行为的宝贵线索。在本文中,我们提出了一种基于宽场荧光显微镜图像的测量和数据分析程序,用于定量区分表现出不同程度旋转流动性的单个分子。我们提出的技术特别适用于分子在比用于记录荧光图像的相机帧率快得多的时间尺度上进行旋转运动的情况。与目前可用的方法不同,不需要用于调制照射样品的光的偏振的复杂硬件。可以在显微镜的成像路径中插入额外的偏振光学元件以实现更高的测量精度,但这不是必需的。我们进行了理论分析,并用典型的单分子成像实验参数进行数值模拟对我们的技术进行了基准测试。