Time-resolved fluorescence spectroscopy and imaging of DNA labeled with DAPI and hoechst 33342 using three-photon excitation

被引:63
作者
Lakowicz, JR
Gryczynski, I
Malak, H
Schrader, M
Engelhardt, P
Kano, H
Hell, SW
机构
[1] UNIV TURKU,CTR BIOTECHNOL,FIN-20521 TURKU,FINLAND
[2] UNIV MARYLAND,SCH MED,DEPT BIOCHEM & MOL BIOL,CTR FLUORESCENCE SPECT,BALTIMORE,MD 21201
[3] UNIV MARYLAND,SCH MED,DEPT BIOCHEM & MOL BIOL,CTR MED BIOTECHNOL,BALTIMORE,MD 21201
[4] UNIV TURKU,DEPT MED PHYS & CHEM,FIN-20521 TURKU,FINLAND
[5] UNIV HELSINKI,HAARTMAN INST,DEPT VIROL,FIN-00014 HELSINKI,FINLAND
关键词
D O I
10.1016/S0006-3495(97)78696-X
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We examined the fluorescence spectral properties of the DNA stains DAPI (4',6-diamidino-2-phenylindole, hydrochloride) and Hoechst 33342 (bis-benzimide, or 2,5'-bi-H-1-benzimidazole2'-(4-ethoxyphenyl)-5-(4-methyl-1-piperazinyl)) with two-photon (2h nu) and three-photon (3h nu) excitation using femtosecond purses from a Ti:sapphire laser from 830 to 885 nm. The mode of excitation of DAPI bound to DNA changed from two-photon at 830 nm to three-photon at 885 nm. In contrast, Hoechst 33342 displayed only two-photon excitation from 830 to 885 nm. DAPI-DNA displayed the same emission spectra and decay times for 2h nu and 3h nu excitation. Hoechst 33342-DNA displayed the same intensity decay for excitation at 830 and 885 nm. Both probes displayed higher anisotropies for multiphoton excitation as compared to one-photon excitation with ultraviolet wavelengths, and DAPI-DNA displays a higher anisotropy for 3h nu at 885 nm than for 2h nu at 830 nm. We used 970-nm excitation of DAPI-stained chromosomes to obtain the first three-dimensional images with three-photon excitation. Three-photon excitation of DAPI-stained chromosomes at 970 nm was demonstrated by the power dependence in the fluorescence microscope.
引用
收藏
页码:567 / 578
页数:12
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