Szmacinski H, Lakowicz J R
Department of Biological Chemistry, University of Maryland School of Medicine, Baltimore, USA.
Cell Calcium. 1995 Jul;18(1):64-75. doi: 10.1016/0143-4160(95)90046-2.
We characterized the fluorescence probe Fura-2 for calcium measurements using frequency-domain phase-modulation fluorometry. By the use of different excitation wavelengths from 345 to 380 nm, the apparent calcium dissociation constants can be altered from 41 nM to 1.92 microM Ca2+. This change in apparent Kd results from changes in the relative extent of excitation of the calcium-bound and calcium-free forms, and the excitation wavelength-dependent contribution of each form to the intensity decay. These results indicate that lifetime-based measurements with Fura-2 can be used for imaging of calcium over a wide range of concentrations. An additional favorable feature of Fura-2 is that the calcium-free form can be almost exclusively excited at wavelength of 390 nm or longer, and can thus be used as a reference providing the lifetime in the absence of calcium, without removing the calcium. Additionally, exposure of Fura-2 to intense illumination shifts but does not distort the frequency response. For cellular imaging, these favorable properties of Fura-2 may allow calibration of the calcium concentrations without the use of ionophores.
我们使用频域相位调制荧光法对用于钙测量的荧光探针Fura-2进行了表征。通过使用345至380 nm的不同激发波长,表观钙解离常数可从41 nM改变至1.92 μM Ca²⁺。表观解离常数(Kd)的这种变化源于钙结合形式和游离钙形式相对激发程度的变化,以及每种形式对强度衰减的激发波长依赖性贡献。这些结果表明,基于寿命测量的Fura-2可用于在广泛的浓度范围内对钙进行成像。Fura-2的另一个有利特性是,游离钙形式几乎可以在390 nm或更长波长下被专门激发,因此可以用作在不存在钙的情况下提供寿命的参考,而无需去除钙。此外,Fura-2暴露于强光下会发生偏移,但不会扭曲频率响应。对于细胞成像,Fura-2的这些有利特性可能允许在不使用离子载体的情况下校准钙浓度。