Colyer Ryan A, Scalia Giuseppe, Kim Taiho, Rech Ivan, Resnati Daniele, Marangoni Stefano, Ghioni Massimo, Cova Sergio, Weiss Shimon, Michalet Xavier
Department of Chemistry & Biochemistry, UCLA, Los Angeles, CA.
Proc SPIE Int Soc Opt Eng. 2010 Jan 23;7571:75710G-75710G11. doi: 10.1117/12.841398.
Solution-based single-molecule spectroscopy and fluorescence correlation spectroscopy (FCS) are powerful techniques to access a variety of molecular properties such as size, brightness, conformation, and binding constants. However, this is limited to low concentrations, which results in long acquisition times in order to achieve good statistical accuracy. Data can be acquired more quickly by using parallelization. We present a new approach using a multispot excitation and detection geometry made possible by the combination of three powerful new technologies: (i) a liquid crystal spatial light modulator to produce multiple diffraction-limited excitation spots; (ii) a multipixel detector array matching the excitation pattern and (iii) a low-cost reconfigurable multichannel counting board. We demonstrate the capabilities of this technique by reporting FCS measurements of various calibrated samples as well as single-molecule burst measurements.
基于溶液的单分子光谱和荧光相关光谱(FCS)是获取多种分子特性(如大小、亮度、构象和结合常数)的强大技术。然而,这仅限于低浓度情况,这导致为了获得良好的统计精度需要较长的采集时间。通过并行化可以更快地采集数据。我们提出了一种新方法,该方法使用由三种强大的新技术组合而成的多点激发和检测几何结构:(i)一种液晶空间光调制器,用于产生多个衍射极限激发光斑;(ii)一个与激发图案匹配的多像素探测器阵列;以及(iii)一个低成本的可重构多通道计数板。我们通过报告各种校准样品的FCS测量结果以及单分子猝发测量结果来展示该技术的能力。