Hadley R W, Kirby M S, Lederer W J, Kao J P
Department of Physiology, University of Maryland School of Medicine, Baltimore 21201.
Biophys J. 1993 Dec;65(6):2537-46. doi: 10.1016/S0006-3495(93)81328-6.
Emission spectra of the photolabile Ca2+ chelators DM-nitrophen, nitr-5, and diazo-2 were studied alone, and in the presence of indo-1, to investigate potential interactions that would make the simultaneous manipulation and ratiometric measurement of the intracellular Ca2+ concentration difficult. Neither diazo-2 nor its photoproduct were found to be significantly fluorescent, and consequently concentrations of diazo-2 up to 20 times that of indo-1 did not distort the emission spectra of indo-1. DM-nitrophen was scarcely fluorescent, but its fluorescence did increase upon photolysis. In contrast to diazo-2 and DM-nitrophen, nitr-5 itself was found to be quite fluorescent, and this fluorescence was significantly increased upon photolysis. Thus, combined use of nitr-5 and indo-1 poses the most difficulty. The emission spectra of all the investigated compounds were used to define experimental conditions and calibration procedures that make possible simultaneous measurement and manipulation of the intracellular Ca2+ concentration.
研究了光不稳定的Ca2+螯合剂DM-硝基苯酚、硝氮唑-5和重氮-2单独存在时以及在吲哚-1存在时的发射光谱,以研究可能导致细胞内Ca2+浓度同时操纵和比率测量困难的潜在相互作用。未发现重氮-2及其光产物有明显荧光,因此,重氮-2浓度高达吲哚-1浓度20倍时也不会扭曲吲哚-1的发射光谱。DM-硝基苯酚几乎没有荧光,但其荧光在光解后确实增强。与重氮-2和DM-硝基苯酚不同,硝氮唑-5本身具有较强荧光,且光解后荧光显著增强。因此,硝氮唑-5和吲哚-1联合使用带来的困难最大。所有研究化合物的发射光谱用于确定实验条件和校准程序,以实现细胞内Ca2+浓度的同时测量和操纵。