Lakowicz J R, Gryczynski I, Gryczynski Z, Dattelbaum J D
University of Maryland School of Medicine, 725 West Lombard Street, Baltimore, Maryland, 21201, USA.
Anal Biochem. 1999 Feb 15;267(2):397-405. doi: 10.1006/abio.1998.3029.
We describe a new approach to fluorescence sensing based on measurements of steady-state anisotropies in the presence of reference fluorophores with known anisotropies. The basic concept is that the anisotropy of a mixture reflects a weighted average of the anisotropies of the emitting species. By use of reference fluorophores the starting anisotropy can be near zero, or near 0.9 for oriented films which contain the reference fluorophore. Changing intensities of the analyte result in changes in anisotropy. A wide dynamic range of anisotropies is available because of the freedom to select high or low starting values. Anisotropy-based sensing was demonstrated for pH using 6-carboxyfluorescein and for protein affinity or immunoassay using an oriented film with high anisotropy and a protein labeled with a metal-ligand complex. The latter measurements were performed with a simple light-emitting diode excitation source without an excitation polarizer. The sensitive range of the assay can be adjusted by changing the intensity of the reference fluorophore. Anisotropy-based sensing can have numerous applications in clinical and analytical chemistry.
我们描述了一种基于在存在具有已知各向异性的参考荧光团的情况下测量稳态各向异性的荧光传感新方法。基本概念是混合物的各向异性反映了发射物种各向异性的加权平均值。通过使用参考荧光团,起始各向异性可以接近零,对于含有参考荧光团的取向膜则接近0.9。分析物强度的变化会导致各向异性的变化。由于可以自由选择高或低的起始值,因此可获得宽范围的各向异性。使用6-羧基荧光素对pH进行了基于各向异性的传感演示,并使用具有高各向异性的取向膜和用金属-配体复合物标记的蛋白质对蛋白质亲和力或免疫测定进行了演示。后者的测量是使用简单的发光二极管激发源进行的,没有激发偏振器。通过改变参考荧光团的强度可以调节测定的敏感范围。基于各向异性的传感在临床和分析化学中可以有许多应用。