Molecular Dynamics of Biological Probes by Fluorescence Correlation Microscopy with Two-Photon Excitation

被引:0
|
作者
E. Guiot
M. Enescu
B. Arrio
G. Johannin
G. Roger
S. Tosti
F. Tfibel
F. Mérola
A. Brun
P. Georges
M. P. Fontaine-Aupart
机构
[1] UMR 8501,Laboratoire Charles Fabry de l'Institut d'Optique
[2] UPR 3361,Laboratoire de Photophysique Moléculaire
[3] Faculté des Sciences,undefined
[4] Laboratoire de Bioénergie Membranaire,undefined
[5] Laboratoire Charles Fabry de l'Institut d'Optique,undefined
[6] UMR 8501,undefined
[7] Laboratoire pour l'Utilisation du Rayonnement Electromagnétique,undefined
来源
Journal of Fluorescence | 2000年 / 10卷
关键词
Two-photon excitation; fluorescence correlation microscopy; translational diffusion; single-molecule detection;
D O I
暂无
中图分类号
学科分类号
摘要
We report on the application of fluorescence correlation microscopy under two-photon excitation of fluorophores of biological interest: FITC–dextran (MW, from 20 to 150 kDa), green fluorescent protein (MW, 27 kDa), and fluorescein (MW, 330 Da). Under these experimental conditions, the translational diffusion coefficients of these molecules in aqueous solutions derived from the fluorescence intensity autocorrelation function were determined for the first time and were found to be 24 × 10−7, 8.2 × 10−7, and 3 × 10−7 cm2 s−1 for 150-kDa FITC–dextran, green fluorescent protein, and fluorescein, respectively. These results are discussed in connection with previously reported results obtained by different methods. The great sensibility of the system has been applied to single-molecule detection of the smaller fluorophore, fluorescein.
引用
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页码:413 / 419
页数:6
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