Sachl Radek, Mikhalyov Ilya, Hof Martin, Johansson Lennart B A
Department of Chemistry, Biophysical Chemistry, Umeå University, S-901 87, Umeå, Sweden.
Phys Chem Chem Phys. 2009 Jun 7;11(21):4335-43. doi: 10.1039/b821658d. Epub 2009 Mar 25.
Ganglioside (G(M1)) micelles have been studied by means of three different techniques: fluorescence correlation spectroscopy (FCS), electronic energy transfer, as monitored by time-resolved fluorescence spectroscopy, as well as static and dynamic light scattering. The aggregation numbers obtained, 168 +/- 4, remain constant over a wide range of G(M1) concentrations (0.764-156 muM), are very consistent when using different donor-acceptor energy transfer pairs and have served as reference values in tests of the FCS method. It is recommended to calibrate the focal volume by using known dye concentrations. For this the rhodamine dye, 5-TAMRA, turns out to be most suitable. It is also shown that FCS provides correct values of the aggregation numbers, provided that the focal volume is calibrated by using updated values of the diffusion constant of Rhodamine 6G. These results also support recent methodological advances in FCS.
已通过三种不同技术对神经节苷脂(G(M1))胶束进行了研究:荧光相关光谱法(FCS)、通过时间分辨荧光光谱监测的电子能量转移以及静态和动态光散射。所获得的聚集数为168±4,在很宽的G(M1)浓度范围(0.764 - 156 μM)内保持恒定,使用不同的供体 - 受体能量转移对时非常一致,并已作为FCS方法测试中的参考值。建议使用已知染料浓度来校准焦体积。为此,罗丹明染料5 - TAMRA被证明是最合适的。还表明,只要通过使用罗丹明6G扩散常数的更新值来校准焦体积,FCS就能提供正确的聚集数。这些结果也支持了FCS最近的方法学进展。