Hwang Ling Chin, Wohland Thorsten
Department of Chemistry, National University of Singapore.
J Chem Phys. 2005 Mar 15;122(11):114708. doi: 10.1063/1.1862614.
It was shown recently that fluorescence cross-correlation spectroscopy (FCCS) can be performed using a single laser wavelength for excitation (SW-FCCS) [L. C. Hwang and T. Wohland, Chem. Phys. Chem 5, 549 (2004).]. This method simplifies the FCCS setup since it does not require the simultaneous alignment of two lasers to the same focal spot. But up to now the method was shown to work only with dyes possessing large Stokes' shifts, and thus was limited to the use of quantum dots and tandem dyes. In this work we show that standard organic dyes with overlapping emission spectra, for instance fluorescein and tetramethylrhodamine, can be used as fluorescent pairs in SW-FCCS. As a biological model system for ligand-receptor interactions we studied the binding of biotin to streptavidin. To investigate the applicability of SW-FCCS for binding studies we adapt the existing FCCS theory for SW-FCCS and calculate limits for the measurement of dissociation constants in dependence on sample concentration, sample purity, and spectral cross talk between the different detection channels.
最近研究表明,荧光交叉相关光谱法(FCCS)可使用单一激光波长进行激发(单波长FCCS)[L.C. 黄和T. 沃兰德,《化学物理化学》5,549(2004年)]。该方法简化了FCCS装置,因为它不需要将两台激光器同时对准同一个焦点。但到目前为止,该方法仅适用于具有大斯托克斯位移的染料,因此仅限于使用量子点和串联染料。在这项工作中,我们表明发射光谱重叠的标准有机染料,例如荧光素和四甲基罗丹明,可作为单波长FCCS中的荧光对。作为配体 - 受体相互作用的生物模型系统,我们研究了生物素与链霉亲和素的结合。为了研究单波长FCCS在结合研究中的适用性,我们将现有的FCCS理论应用于单波长FCCS,并根据样品浓度、样品纯度以及不同检测通道之间的光谱串扰计算解离常数测量的极限。