Hirshfield K M, Toptygin D, Packard B S, Brand L
Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218.
Anal Biochem. 1993 Mar;209(2):209-18. doi: 10.1006/abio.1993.1109.
A fluorescence technique for characterizing ligand binding is evaluated. This technique uses the combination of steady-state and time-resolved methods to recover molar concentrations and overcomes errors inherent in the use of either method alone. The technique is applicable to time-resolved measurements made either with time-domain or frequency-domain instrumentation. A straightforward single-frequency phase/modulation approach is presented to determine whether an experimental system can be described by a two-state system. The approach is based on a nonlinear transformation of the phase/modulation data that results in a linear model function. Here, the theory is applied to the fluorescent calcium-binding probes Quin-2 and Calcium Green, but is relevant to studies involving other interacting systems. The technique described is used to assess the fraction of bound ligand (Ca2+) and binding constants for these probes.
对一种用于表征配体结合的荧光技术进行了评估。该技术结合了稳态和时间分辨方法来测定摩尔浓度,并克服了单独使用任何一种方法时固有的误差。该技术适用于使用时域或频域仪器进行的时间分辨测量。提出了一种简单的单频相位/调制方法,以确定实验系统是否可以用双态系统来描述。该方法基于相位/调制数据的非线性变换,从而得到一个线性模型函数。在此,该理论应用于荧光钙结合探针喹啉-2和钙黄绿素,但与涉及其他相互作用系统的研究相关。所描述的技术用于评估这些探针的结合配体(Ca2+)分数和结合常数。